USE OF A TRUNCATED EIF-5A1 POLYNUCLEOTIDE TO INDUCE APOPTOSIS IN CANCER CELLS

Abstract

The present invention relates to the combinatorial use of an siRNA targeted against an endogenous gene to knock out or knock down expression of the endogenous gene in a host and a delivery of a polynucleotide encoding the gene in a delivery vehicle/expression vector to the host to provide expression in the host of the protein encoded by the polynucleotide. The present invention also relates to a truncated form of eIF-5A1 that is useful for inducing apoptosis and killing of cells, especially cancer cells in a mammal.

Description

RELATED APPLICATIONS

This application claims priority to U.S. provisional application 61/093,749, which was filed on Sep. 3, 2008, and U.S. application Ser. No. 12/400,742 filed on Mar. 19, 2009, which are herein incorporated by reference in its entirety.

BACKGROUND OF THE INVENTION

Relatively recently, researchers observed that double stranded RNA (“dsRNA”) could be used to inhibit protein expression. This ability to silence a gene has broad potential for treating human diseases, and many researchers and commercial entities are currently investing considerable resources in developing therapies based on this technology.

Double stranded RNA induced gene silencing can occur on at least three different levels: (i) transcription inactivation, which refers to RNA guided DNA or histone methylation; (ii) siRNA induced mRNA degradation; and (iii) mRNA induced transcriptional attenuation.

It is generally considered that the major mechanism of RNA induced silencing (RNA interference, or RNAi) in mammalian cells is mRNA degradation. Initial attempts to use RNAi in mammalian cells focused on the use of long strands of dsRNA. However, these attempts to induce RNAi met with limited success, due in part to the induction of the interferon response, which results in a general, as opposed to a target-specific, inhibition of protein synthesis. Thus, long dsRNA is not a viable option for RNAi in mammalian systems.

More recently it has been shown that when short (18-30 bp) RNA duplexes are introduced into mammalian cells in culture, sequence-specific inhibition of target mRNA can be realized without inducing an interferon response. Certain of these short dsRNAs, referred to as small inhibitory RNAs (“siRNAs”), can act catalytically at sub-molar concentrations to cleave greater than 95% of the target mRNA in the cell. A description of the mechanisms for siRNA activity, as well as some of its applications are described in

Provost et al. (2002) Ribonuclease Activity and RNA Binding of Recombinant Human Dicer, EMBO J. 21(21): 5864-5874; Tabara et al. (2002) The dsRNA Binding Protein RDE-4 Interacts with RDE-1, DCR-1 and a DexH-box Helicase to Direct RNAi in C. elegans, Cell 109(7):861-71; Ketting et al. (2002) Dicer Functions in RNA Interference and in Synthesis of Small RNA Involved in Developmental Timing in C. elegans; Martinez et al., Single-Stranded Antisense siRNAs Guide Target RNA Cleavage in RNAi, Cell 110(5):563; Hutvagner & Zamore (2002) A microRNA in a multiple-turnover RNAi enzyme complex, Science 297:2056.

From a mechanistic perspective, introduction of long double stranded RNA into plants and invertebrate cells is broken down into siRNA by a Type III endonuclease known as Dicer. Sharp, RNA interference—2001, Genes Dev. 2001, 15:485. Dicer, a ribonuclease-III-like enzyme, processes the dsRNA into 19-23 base pair short interfering RNAs with characteristic two base 3′ overhangs. Bernstein, Caudy, Hammond, & Hannon (2001) Role for a bidentate ribonuclease in the initiation step of RNA interference, Nature 409:363. The siRNAs are then incorporated into an RNA-induced silencing complex (RISC) where one or more helicases unwind the siRNA duplex, enabling the complementary antisense strand to guide target recognition. Nykanen, Haley, & Zamore (2001), ATP requirements and small interfering RNA structure in the RNA interference pathway, Cell 107:309. Upon binding to the appropriate target mRNA, one or more endonucleases within the RISC cleaves the target to induce silencing. Elbashir, Lendeckel, & Tuschl (2001) RNA interference is mediated by 21- and 22-nucleotide RNAs, Genes Dev. 15:188, FIG. 1.

The interference effect can be long lasting and may be detectable after many cell divisions. Moreover, RNAi exhibits sequence specificity. Kisielow, M. et al. (2002), Isoform-specific knockdown and expression of adaptor protein ShcA using small interfering RNA, J. Biochem. 363:1-5. Thus, the RNAi machinery can specifically knock down one type of transcript, while not affecting closely related mRNA. These properties make siRNA a potentially valuable tool for inhibiting gene expression and studying gene function and drug target validation. Moreover, siRNAs are potentially useful as therapeutic agents against: (1) diseases that are caused by over-expression or misexpression of genes; and (2) diseases brought about by expression of genes that contain mutations.

Successful siRNA-dependent gene silencing depends on a number of factors. One of the most contentious issues in RNAi is the question of the necessity of siRNA design, i.e., considering the sequence of the siRNA used. Early work in C. elegans and plants circumvented the issue of design by introducing long dsRNA (see, for instance, Fire, A. et al. (1998) Nature 391:806-811). In this primitive organism, long dsRNA molecules are cleaved into siRNA by Dicer, thus generating a diverse population of duplexes that can potentially cover the entire transcript. While some fraction of these molecules are non-functional (i.e., induce little or no silencing) one or more have the potential to be highly functional, thereby silencing the gene of interest and alleviating the need for siRNA design. Unfortunately, due to the interferon response, this same approach is unavailable for mammalian systems. While this effect can be circumvented by bypassing the Dicer cleavage step and directly introducing siRNA, this tactic carries with it the risk that the chosen siRNA sequence may be non-functional or semi-functional.

A number of researches have expressed the view that siRNA design is not a crucial element of RNAi. On the other hand, others in the field have begun to explore the possibility that RNAi can be made more efficient by paying attention to the design of the siRNA.

To treat various diseases or disorders, the upregulation of certain proteins is desirable but this may not be all that is needed. For example, the combinatorial use of siRNA to knock down or knock out expression of an endogenous protein or a different protein may be needed. The present invention fulfills this need and provides methods of treating cancer, especially multiple myeloma.

Cancer, including multiple myeloma are diseases which would benefit from the ability to induce apoptosis. Conventional therapies for of multiple myeloma include chemotherapy, stem cell transplantation, high-dose chemotherapy with stem cell transplantation, and salvage therapy. Chemotherapies include treatment with Thalomid®(thalidomide), bortezomib, Aredia® (pamidronate), steroids, and Zometa® (zoledronic acid). However many chemotherapy drugs are toxic to actively dividing non-cancerous cells, such as of the bone marrow, the lining of the stomach and intestines, and the hair follicles. Therefore, chemotherapy may result in a decrease in blood cell counts, nausea, vomiting, diarrhea, and loss of hair.

Conventional chemotherapy, or standard-dose chemotherapy, is typically the primary or initial treatment for patients with of multiple myeloma. Patients also may receive chemotherapy in preparation for high-dose chemotherapy and stem cell transplant. Induction therapy (conventional chemotherapy prior to a stem cell transplant) can be used to reduce the tumor burden prior to transplant. Certain chemotherapy drugs are more suitable for induction therapy than others, because they are less toxic to bone marrow cells and result in a greater yield of stem cells from the bone marrow. Examples of chemotherapy drugs suitable for induction therapy include dexamethasone, thalidomide/dexamethasone, VAD (vincristine, Adriamycin® (doxorubicin), and dexamethasone in combination), and DVd (pegylated liposomal doxorubicin (Doxil®, Caelyx®), vincristine, and reduced schedule dexamethasone in combination).

The standard treatment for of multiple myeloma is melphalan in combination with prednisone (a corticosteroid drug), achieving a response rate of 50%. Unfortunately, melphalan is an alkylating agent and is less suitable for induction therapy. Corticosteroids (especially dexamethasone) are sometimes used alone for multiple myeloma therapy, especially in older patients and those who cannot tolerate chemotherapy. Dexamethasone is also used in induction therapy, alone or in combination with other agents. VAD is the most commonly used induction therapy, but DVd has recently been shown to be effective in induction therapy. Bortezomib has been approved recently for the treatment of multiple myeloma, but it is very toxic. However, none of the existing therapies offer a significant potential for a cure. Thus, there still remains a need to find a suitable treatment for cancer and multiple myeloma. The present invention fulfills this need.

SUMMARY OF INVENTION

The present invention provides an isolated polynucleotide encoding a truncated form of eIF-5A1 as well as a truncated eIF-A1 polypeptide. The truncated eIF-5A1 polynucleotide is useful in inducing apoptosis and killing cancer cells in a subject The truncated polynucleotide may be used within an expression vector which is then administered to a subject. The truncated eIF-5A form is expressed within the mammal and kills cancer cells. The truncated eIF-5A1 protein is about 16 kDA as opposed to the full length eIf-5A1 protein, which is about 17 kDa. A polynucleotide encoding a truncated eIF5A1 protein may be used to make a medicament used to induce apoptosis in a cancer cell or a tumor in a subject. The polynucleotide encoding a truncated eIF5A1 protein may be used in conjunctions with other embodiments described herein (for example in combination with a polynucleotide encoding full length eIF5A1, with a polynucleotide encoding full length mutant eIF5A1, and/or with an siRNA targeted against the 3′UTR of eIF5A).

The present invention also relates to the combinatorial use of an siRNA targeted against an endogenous gene to knock out or knock down expression of the endogenous gene in a host and a delivery of a polynucleotide encoding the gene in a delivery vehicle/expression vector to the host to provide expression in the host of the protein encoded by the polynucleotide. A polynucleotide encoding a normal (non faulty) protein (or the protein itself) is administered to the host and is expressed (in the case of the polynucleotide) so that the normal protein can perform its necessary function. The siRNA is preferably designed to target a region of the gene so it either knocks down or knocks out endogenous expression of the faulty protein but at the same time will not effect exogenous expression of the administered polynucleotide encoding the normal protein.

The invention provides a composition comprising a complex of an eIF5A1 siRNA targeted against the 3′ end of eIF5A1, an expression vector comprising a polynucleotide encoding a mutant eIF5A1 wherein the mutant eIF5A1 is unable to be hypusinated, and wherein the siRNA and the expression vector are complexed to polyethylenimine to form a complex.

The invention provides a composition comprising an siRNA targeted against a target gene to suppress endogenous expression of the target gene is a subject, and a polynucleotide encoding a target protein capable of being expressed in the subject. In certain embodiments the polynucleotide is in RNAi resistant plasmid (will not be suppressed by the siRNA). The siRNA and the plasmid are preferably complexed to polyethylenimine to form a complex.

In certain embodiments the siRNA has the sequence shown in FIG. 25 and wherein the polynucleotide encoding the mutant eIF5A1 is eIF5A1^K50R. The expression vector comprises a polynucleotide encoding a mutant eIF5A1 and a promoter operably linked to provide expression of the polynucleotide in a subject. The promoter preferably is either tissue specific or systemic. For example, if the composition is used to treat cancer, then preferably the promoter is tissue specific for the tissue in which the cancer resides. For example, for treating multiple myeloma, it is preferable to use a B cell specific promoter, such as B29. In certain embodiments, the expression vector comprises a pCpG plasmid.

In certain embodiments, the eIF5A1 siRNA and the expression vector comprising the mutant eIF5A1 polynucleotide are independently complexed to polyethylenimine, such as in vivo JetPEI™. In other embodiments, the eIF5A1 siRNA and the expression vector comprising the mutant eIF5A1 polynucleotide are complexed together to polyethylenimine.

The present invention further provides a composition comprising an eIF5A1 siRNA targeted against the 3′ end of eIF5A1 and an expression vector comprising a polynucleotide encoding a mutant eIF5A1 wherein the mutant eIF5A1 is unable to be hypusinated, and wherein the siRNA and the expression vector are delivered to a subject to treat cancer. The cancer may be any cancer including multiple myeloma.

The present invention further provides a method of treating cancer comprising administering composition of the present invention to a subject (including but not limited to mammals and humans).

The composition may be administered any acceptable route, such as, but not limited to intravenously, intra peritoneally, subcutaneously or intra tumorally. The siRNA and the expression vector may be administered at different times and via different routes or may be administered together at the same time and via the same route. For example, but not limited to, the siRNA may be delivered naked or complexed to a carrier such as in vivo jetPEI via IV and the expression vector may be administered intra tumorally, or both the siRNA and the expression vector may be administered IV or intratumorally, etc.

The present invention provides a method of inhibiting cancer cell growth and/or killing cancer cells. The present invention also provides a method of inhibiting or slowing down the ability of a cancer cell to metastasize. Inhibiting cancer growth includes a reduction in the size of a tumor, a decrease in the growth of the tumor, and can also encompass a complete remission of the tumor. The cancer can be any cancer or tumor, including but not limited to colon cancer, colorectal adenocarcinoma, bladder carcinoma, cervical adenocarcinoma, and lung carcinoma. Preferably the cancer is multiple myeloma.

In preferred embodiments, the eIF-5A is a mutant that is unable to be hypusinated. Exemplary mutants are described herein.

In addition to providing eIF-5A or a polynucleotide encoding eIF-5A to a subject (to provide expression of the eIF-5A), siRNA is provided to knock out or knock down endogenous expression of eIF-5A.

The present invention also provides the use of eIF5A, polynucleotides encoding eIF5A1 and siRNA against eIF5A1 to make a medicament to treat cancer kill multiple myeloma cells in a subject having multiple myeloma. Preferably the polynucleotides encoding a mutant eIF-5A are unable to be hypusinated.

The present invention also provides a method of treating sickle cell anemia. A polynucleotide encoding a healthy hemoglobin gene (such as HBB) is administered to a patient suffering from sickle cell anemia. In conjunction, the patient is also administered siRNA that targets the gene encoding the faulty hemoglobin gene (such as the gene encoding the mutant HbS) to knock down or knock out expression of the faulty protein. The treatment may further comprise administration of other known medicines or treatments commonly used in treating sickle cell anemia.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 provides the amino acid sequence of human eIF-5A1 and shows various important sites.

FIGS. 2A and 2B show that mutation of eIF-5A1 at K50 and K67 increases accumulation of transfected protein. See example 1.

FIG. 3 shows that mutation of eIF5A1 at K47, K50 and K67 increases accumulation of transfected protein. See example 2.

FIG. 4 shows that mutation of eIF5A1 at K50 and K67 results in induction of apoptosis when transfected into KAS cells. See example 3.

FIG. 5 shows that mutation of eIF5A1 at K50 and K67 results in induction of apoptosis when transfected into KAS cells. See example 4.

FIG. 6 shows that mutation of eIF5A1 at K50 and K67 results in induction of apoptosis when transfected into KAS cells. See example 5.

FIG. 7A shows transfection with siRNA and treating with an adenovirus that is modified to express eIF-5A1 results in apoptosis in KAS cells. See example 6A. FIG. 7B shows that pre-treatment with eIF5A1 siRNA (against target #1 (SEQ ID NO:1)) (the sequence of the siRNA construct shown in FIG. 25 reduced expression of endogenous eIF5A1 but allows accumulation of RNAi-resistant eIF5A1^k50A expressed by adenovirus. See example 6B. FIG. 7C shows that pre-treatment with eIF5A1 siRNA against target #1 prior to adenovirus infection reduces expression of phosphorylated NF-κB in human multiple myeloma cells. See example 6C. FIG. 7D shows that pre-treatment with eIF5A1 siRNA against target #1 prior to Adenovirus infection reduces expression of phosphorylated NF-kB and ICAM-1 in human multiple myeloma cells. See example 6D. FIG. 7E shows that siRNA-mediated suppression of eIFSA in human multiple myeloma cells inhibits LPS-mediated induction of NFkB DNA-Binding Activity. The inhibition of NFkB activity by eIFSA siRNA could explain it's ability to increase apoptosis induction when combined with over-expression of eIF5A^K50R since NF-kB regulates many pro-survival and anti-apoptosis pathways. FIG. 7F shows that pretreatment of KAS cells with siRNA increases apoptosis by eIF5A1^k50R gene delivery in the presence of IL-6. See example 6E.

FIG. 8 shows that co-administration of eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors. The data shown is the tumor volume for all the mice in each group. See example 7.

FIG. 9 shows that co-administration of eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors. The data shown is the average tumor volume per group+/−standard error. See example 7.

FIG. 10 shows that co-administration of eIF5A1 plasmid and eIF5A1 siRNA reduces weight of multiple myeloma subcutaneous tumors. See example 7.

FIG. 11 shows that co-administration of eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors and results in tumor shrinkage. See Example 8.

FIG. 12 shows that administration of eIF5A1 siRNA intra-venously (i.v.) and PEI/eIF5A1K50R plasmid complexes intra-tumorally (i.t.) results in tumor shrinkage of multiple myeloma subcutaneous tumors. See example 9.

FIG. 13A shows that treatment with eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors and results in tumor shrinkage. FIG. 13B shows that co-administration of eIF5A1 plasmid and eIF5A1 siRNA results in tumor shrinkage. FIG. 13C shows that administration of eIF5A1 siRNA intra-venously (i.v.) and PEI/eIF5A1^K50R plasmid complexes intra-tumorally (i.t.) results in tumor shrinkage of multiple myeloma subcutaneous tumors.

FIG. 14 shows that intra-venous co-administration of eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors. See example 10.

FIG. 15 shows that administration of eIF5A1 siRNA intra-venously (i.v.) and PEI/eIF5A1K50R plasmid complexes intra-venously (i.v.) or intra-peritoneal (i.p.) delays growth of multiple myeloma subcutaneous tumors. See example 11.

FIG. 16 shows that treatment with eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors.

FIGS. 17A and 17B show that co-administration of eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors and results in tumor shrinkage. See example 12.

FIGS. 18A and 18B show that administration of eIF5A1 siRNA intra-venously (i.v.) and PEI/eIF5A1K50R plasmid complexes intra-tumorally (i.t.) results in tumor shrinkage of multiple myeloma subcutaneous tumors. See example 13.

FIG. 19 shows co-administration of eIF5A1^K50R plasmid, driven by either the EF1 or B29 promoter, and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors and results in tumor shrinkage (KAS-SQ-5). See example 14.

FIG. 20 shows co-administration of eIF5A1 siRNA increases anti-tumor effect of eIF5A1^K50R plasmid, driven by either the EF1 or B29 promoter, on multiple myeloma subcutaneous tumors and results in reduced tumor burden (KAS-SQ-5). See example 15.

FIG. 21 shows eIF5A1 siRNA synergistically increases apoptosis resulting from infection with Ad-eIF5A in lung adenocarcinoma cells. See example 16.

FIG. 22 shows the map of pExp5A, the construction of which is described in Example 17.

FIG. 23 shows the predicted sequence of pExp5A (3371 bp). See example 17.

FIGS. 24A and 24B show the expression of eIF5A1^K50R in various cell lines. See example 18.

FIG. 25 shows the target sequence and the sequence of a preferred eIF5A1 siRNA.

FIG. 26 provides the results of efficacy studies in multiple myeloma. See example 21.

FIG. 27 provides the results of efficacy studies in multiple myeloma. See example 21.

FIG. 28 provides the sequence of eIF-5A1^K50R cDNA.

FIG. 29 provides the alignment of human eIF-5A1 against human eIF5A1^K50R.

FIG. 30 shows the effect of DNA:siRNA ratio on HA-eIF5A^K50R expression. See example 23.

FIG. 31 shows the effect of DNA:siRNA ratio on apoptosis induced by nanoparticle transfection. See example 24.

FIG. 32 shows administration of PEI complexes (N/P=6 or 8) containing eIF5A1K50R plasmid and eIF5A1 siRNA (siSTABLE or non-siSTABLE) inhibits growth of multiple myeloma subcutaneous tumors and results in tumor shrinkage. See example 25.

FIG. 33 shows that the JET PEI™ nanoparticles are being effectively taken up by tumor tissue and that nanoparticles are delivering plasmid and siRNA to the same cell. See example 26.

FIG. 34 shows that KAS cells undergo apoptosis in response to Actinomycin D. KAS cells were either left untreated or were treated with 0.5 μg/ml Actinomycin D. Twenty-four hours after the initiation of treatment, the cells were harvested, washed, and apoptotic cells were labeled using Annexin/PI (BD Bioscience) and analyzed by flow cytometry.

FIG. 35 shows that a truncated form of eIF-5A1 accumulates in response to actinomycin D treatment. KAS cells were treated with 0.5 μg/ml Actinomycin D for time periods ranging from 0 hours to 30 hours. Cell lysate was harvested and analyzed by Western blot using an antibody against eIF5A1. Accumulation of a smaller molecular weight (cleaved) form of eIF5A1 was observed beginning at approximately 8 hours after Actinomycin D treatment and was present throughout the remainder of the treatment. Equal loading is demonstrated by Western blot of the same membrane using an antibody against actin.

FIG. 36 shows that the truncated form of eIF-5A1 has a higher isoelectric point than the full length eIf-5A1. KAS cells were either left untreated or were treated with 0.5 μg/ml Actinomycin D. Seventeen hours after the initiation of treatment, the cell lysates were harvested and separated by 2-D gel electrophoresis followed by Western blot analysis using an antibody against eIF5A1. A large amount of the full-length eIF5A1 can be observed in the untreated sample while accumulation of a cleaved form of eIF5A1 with a higher pI can be observed in the Actinomycin D-treated sample.

FIG. 37 provides a photograph of the truncated eIF-5A1 2-D gel. KAS cells were treated with 0.5 μg/ml Actinomycin D. Seventeen hours after the initiation of treatment, the cell lysate was harvested and separated by 2-D gel electrophoresis followed by Coomassie Blue staining. The position of the cleaved form of eIF5A1 that was collected for mass spectrometry analysis is indicated.

FIG. 38 provides the results of sequencing by mass spectrometry of the truncated eIF-5A1. (A) The full-length amino acid sequence of eIF5A1 is shown in black. Sequenced peptides identified by Mass spectrometry (B) that aligned with the full-length sequence of eIF5A1 are shown in underlined (A). Note that the first six amino acids of eIF5A1 are missing from the sequenced peptides.

FIG. 39 shows that caspase 3, 8 and 9 inhibitors inhibit formation of the truncated form of eIF-5A1. Human multiple myeloma KAS cells were incubated with different caspase inhibitors 8 hours before being co-treated with 0.5 μg/ml Actinomycin D (ActD) for another 16 hours. Cell lysates were collected. Proteins were isolated by 2D-PAGE and subjected to western analysis using antibody against eIF5A. The caspase inhibitors used were Z-VAD-FMK (general caspase inhibitor), Z-LEHD-FMK (caspase 9 inhibitor), Z-DEVD-FMK (caspase 3/7 inhibitor), Z-IETD-FMK (caspase 6/8 inhibitor), and Z-YVAD-FMK (caspase 1 inhibitor). Data indicated that the general caspase inhibitor and inhibitors for caspase 3, 8 and 9 all strongly prevent the formation of the cleavage form of eIF5A that accumulates during ActD-induced apoptosis in KAS cells. Caspase 1 inhibitor also reduces, but not complete blocks, the formation of the cleavage product. These results indicate that eIF5A1 is cleaved by caspases following genotoxic stress (induced by Actinomycin D); cleavage of eIF5A1 could alter its activity ie increase pro-apoptotic activity.

FIG. 40 shows that a deacetylase inhibitor (nicotinamide) promotes formation of the truncated form of eIF-5A1. eIF5A which can be acetylated on Lysine47 is a substrate of a Sir2-related deacetylase Hst2 (Shirai et al., 2008). Human cervical carcinoma Hela S3 cells were treated with 0.5 μg/ml Actinomycin D (ActD) and/or 20 uM nicotinamide, a potent inhibitor of Sir2, for indicated lengths of time. Cell lysates were collected. Proteins were isolated by 2D-PAGE and subjected to western analysis using antibody against eIF5A. Treatment of Hela S3 cells with ActD or nicotinamide alone does not induce the accumulation of the cleavage form of eIF5A. However, in HeLa cells treated with both Actinomycin D and nicotinamide, the cleavage form of eIF5A is up-regulated at least 4 hours after being exposed to ActD, suggesting that acetylation may promote the cleavage of eIF5A during apoptosis.

FIG. 41 provides the DNA sequence of truncated human eIF5A1.

FIG. 42 provides the protein sequence of full length eIF5A1, truncated eIF5As and the cleavage cite.

FIG. 43: Infection of Hela cells with adenovirus constructs results in accumulation of eIF5A transgene. Hela S3 cells were infected with different adenovirus constructs at 500 infectious units per cell. Cell lysates were collected at 48 and 72 hours after infection and subjected to SDS-PAGE and western blotting analysis using antibodies against eIF5A and actin. Accumulation of truncated eIF5A can be observed.

FIG. 44: Induction of apoptosis through treatment with Actinomycin D, sodium nitroprusside, or withdrawal of IL-6 results in the accumulation of a truncated form of eIF5A1 (eIF5A1AΔ1-6) in human myeloma cells. KAS-6/1 cells were treated as indicated and then subjected to 2D-PAGE and western blotting analysis using antibody against eIF5A. Induction of apoptosis in KAS-6/1 cells via with Actinomycin D, the NO donor, sodium nitroprusside, or IL-6 starvation all induced the accumulation of truncated eIF5A1. Over-expression of truncated eIF5A1 using either Ad-A1 Δ(2-6) or Ad-A1 Δ(2-6)/K50R induced the accumulation of eIF5A1 proteins have a smaller pI than the truncated eIF5A1(eIF5A1Δ1-6) produced during apoptosis, indicating that other post-translational modifications are present on eIF5A1Δ1-6).

FIG. 45: eIF5A1D6E and eIF5A1D6E/K50R are resistant to Actinomycin D-induced cleavage during apoptosis. Human multiple myeloma KAS-6/1 cells were treated as indicated and then subjected to 2D-PAGE and western blot analysis using antibody against eIF5A. Over-expressed eIF5A1 (Ad-A1) is subjected to cleavage during treatment with Actinomycin D. However, eIF5A1D6E or eIF5A1D6E/K50R are resistant to cleavage following treatment with Actinomycin D. These results are consistent with the hypothesis that amino acids 3 to 6 of eIF5A1 constitute a caspase cleavage site.

FIG. 46: eIF5A1 is cleaved in vitro by recombinant caspases. Human eIF5A1 (A1) and the mutants eIF5A1D6E (D6E) and eIF5A1D6E/K50R (D6E/KSOR) were subcloned into the pHM6 vector (Roche) which results in expression of an HA-tagged protein. pHM6-HA-A1, pHM6-HA-A1(D6E), and pHM6-HA-A1(D6E/KSOR) were in vitro transcribed and translated (TNT T7 Quick Coupled Transcription/Translation Systems; Promega) and labelled with Transcend Non-Radioactive Translation Detection Systems (Promega) following the manufacturer's instructions. Three microliters of each the in vitro translation products were incubated with one microliter of recombinant caspase (caspases 1, 2, 3, 6, 7, 8, 9, or 10; Calbiochem) in caspase reaction buffer (50 mM Hepes, 0.1% CHAPS, 10% sucrose, 100 mM NaCl, 10 mM DTT, 1 mM EDTA) at 37° C. for 2 hours. Final products were subjected to SDS-PAGE, and the biotinylated proteins were visualized by incubation with Streptavidin-HRP, followed by chemiluminescent detection. The wild-type eIF5A1 is cleaved by caspases 2, 3, 6, 7, 8, 9, and 10 but not by caspase 1. HA-tagged eIF5A1D6E and eIF5A1D6E/K50R are effectively cleaved in vitro by caspases 3, 7 and 8 but are not efficiently cleaved by caspases 9 and 10. However, this cleavage may be due to the highly abundant caspase activity in the in vitro system as well as the high structural similarity between glutamic acid and aspartic acid, thereby allowing cleavage of eIF5A1D6E, although at a reduced efficiency (particularly since eIF5A1D6E and eIF5A1D6E/K50R were resistant to cleavage in an in vivo assay (FIG. 45).

FIG. 47: Infection of Hela cells with Ad-eIF5A1Δ(2-6) or Ad-eIF5A1K50RΔ(2-6) results in increased apoptosis compared to infection with wild-type Ad-eIF5A1 or Ad-eIF5A1K50R. Human cervical cancer Hela S3 cells were infected with different adenovirus constructs at 500 infectious units per cell. At 48 or 72 hours after infection, cells were collected and subjected to Annexin V/PI staining Cells were then sorted by flow cytometry. Percentages of cells at early stage of apoptosis (Annexin V+/PI−), as well as cells at late stage of apoptosis (Annexin V+/PI+) are shown. Truncation of amino acids 2 to 6 increases the apoptotic activity of eIF5A1 or eIF5A1K50R. Conversely, mutation of the predicted cleavage site reduces, but does not eliminate, the apoptotic activity of eIF5A1 or eIF5A1K50R. These results indicate that caspase-mediated cleavage of eIF5A1 results in a truncated form of eIF5A1 with increased apoptotic activity.

FIG. 48 provides a model of the contribution of caspase-mediated truncation of eIF-5A1 in apoptosis.

FIG. 49 shows that cleaved eIF5A accumulates in the nucleus following actinomycin D treatment in KAS human myeloma cells.

FIG. 50 shows that cleaved eIF5A accumulates in the nucleus following actinomycin D treatment in KAS human myeloma cells. Key: UN=untreated; actD=treatment with actinomycin D; C=cytoplasmic fraction; N=nuclear fraction, α-tubilin and α-PCNA are controls. This figure also shows that the truncated form accumulates predominantly in the nucleus, while the full length eIF5A is evenly distributed between the cytoplasm and nucleus.

FIG. 51 shows that the truncated form of eIF5A accumulates in response to different apoptotic stimuli in multiple cell lines and cell types indicating that caspase-mediated cleavage of eIF5A is a common phenomena during apoptosis. This figure also shows that the truncated form accumulates predominantly in the nucleus, while the full length eIF5A is evenly distributed between the cytoplasm and nucleus.

FIG. 52 provides results of a study that shows truncated eIF5A is produced in different cell lines in response to different apoptotic stimuli—KAS human multiple myeloma cells following treatment with IL-6 starvation or IL-6 and FBS starvation and in UACC 1598 (human ovarian cancer cell line) following treatment with actinomycin D.

FIG. 53 provides the nucleotide sequence of human eIF5A1 and eIF5A2.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides an isolated polynucleotide encoding a truncated form of eIF-5A1 as well as a truncated eIF-A1 polypeptide. The truncated eIF-5A1 polynucleotide is useful in inducing apoptosis and killing cancer cells. The truncated polynucleotide may be used within an expression vector which is then administered to a mammal. The truncated eIF-5A form is expressed within the mammal and kills cancer cells. The truncated eIF-5A1 protein is about 16 kDA as opposed to the full length eIf-5A1 protein, which is about 17 kDa.

Formation of a smaller molecular weight form of eIF5A (˜16 kDa) has been observed in cells undergoing apoptosis. This has been observed in beta islet cells treated with a cytokine cocktail and in human myeloma cells (KAS cells) treated with the cytotoxic drug, Actinomycin D. See FIG. 35. The smaller molecular weight form of eIF5A has also been found to accumulate in HeLa cervical cancer cells undergoing apoptosis following infection with Ad-eIF5A1, suggesting that the smaller molecular weight form of eIF5A results from cleavage by proteases rather than being the result of alternative splicing. The observation that the accumulation of the smaller molecular weight form of eIF5A is accompanied by a dramatic reduction in the amount of full-length hypusinated eIF5A further supports that the smaller molecular weight form of eIF5A is due to cleavage rather than alternative splicing. See FIG. 36.

The present invention provides a composition comprising an eIF5A1 polynucleotide that encodes a truncated eIF5A1 protein. This composition is useful to make a medicament used to induce apoptosis in a cancer cell or a tumor in a subject. The eIF5A1 polynucleotide encodes a truncated eIF5A1 protein preferably comprising the amino acid sequence set forth in SEQ ID NO:37 shown in FIG. 38. In certain embodiments, the eIF5A1 polynucleotide encodes a truncated eIF5A1 protein that is about 16 kDA.

The composition and or the medicament can be administered to mammals, including humans. As used herein, “subject” includes mammals and humans.

Inducing apoptosis can have the following effects in a cancer cell or tumor: slows cancer cell or tumor growth, arrests cancer cell or tumor cell growth, or kills the cancer cell or reduces the tumor size and any combination of the above. Any cancer can be treated and in certain embodiments, the cancer is multiple myeloma.

In certain embodiments the eIF5A1 polynucleotide comprises the sequence set forth in SEQ ID NO:38 (as shown in FIG. 41). In certain embodiments the eIF5A1 polynucleotide is comprised within a plasmid or expression vector. Plasmids and expression vectors are described herein below in more detail. In certain embodiments the expression vector is an adenovirus expression vector or is pHM6. In certain embodiments the expression vector comprise a tissue specific promoter, such as a B cell specific promoter (i.e. B29) when the composition or medicament is used to treat multiple myeloma. The expression vector may comprise a pCpG plasmid. As discussed in more detail hereinbelow, the expression vector may be complexed to polyethylenimine.

The composition or medicament is preferably administered intratumorally, intravenously or subcutaneously.

The present invention also provides an isolated polynucleotide encoding a truncated eIF5A1 protein wherein the polynucleotide comprises the sequence set forth in SEQ ID NO:38 (as shown in FIG. 41).

The invention also provides an isolated polynucleotide encoding a truncated eIF5A1 protein wherein the truncated protein comprises the amino acid sequence set forth in SEQ ID NO:37.

As discussed hereinbelow, the eIF5A1 is formed by caspase-mediated cleavage. Accordingly the present invention further provides an isolated truncated eIF5A1 polypeptide formed by caspase mediated cleavage of eIF5A1.

The present invention further provides a composition or the use of the composition to make a medicament comprising an eIF5A1 polynucleotide that encodes a truncated eIF5A1 protein in combination with a full length eIF5A1 polynucleotide. This composition is useful to make a medicament to induce apoptosis in a cancer cell or tumor in a subject. The eIF5A1 polynucleotide encoding a truncated eIF5A protein is as described above. The full length eIF5A1 polynucleotide encodes a protein comprising the amino acid sequence set forth in SEQ ID NO:35. The full length eIF5A1 polynucleotide is described in more detail below. In certain embodiments, the eIF5A1 polynucleotide comprises the sequence set forth in SEQ ID NO:38 and the full length eIF5A1 polynucleotide comprises sequence set forth SEQ ID NO:43 (as shown in FIG. 53).

The full length and truncated polynucleotides may be present in expression vectors as described herein. Additionally the vectors may comprise the promoters described herein as well as any other useful promoter.

In certain embodiments, the full length eIF5A polynucleotide encodes a mutant eIF5A1, wherein the mutation prevents or inhibits hypusination by deoxyhypusine synthase and/or wherein the mutation is present at the ubiquinization site and/or the acetylation site. The mutants are described in more detail below. In certain embodiments, the mutant is selected from the group consisting of K50A, K50R, K67A, K47R, K67R, K50A/K67A, K50A/K47R, K50A/K67R, K50R/K67A, K50R/K47R, K50R/K67R, and K47A/K67A.

The present invention also provides a composition comprising a polynucleotide encoding a truncated eIF5A, a nucleotide encoding a mutant eIF5A and an siRNA targeted against the 3′UTR of eIF5A. The combination/dual use of a nucleotide encoding a mutant eIF5A and an siRNA targeted against the 3′UTR of eIF5A is described more fully below. The composition is useful to make a medicament to administer to a subject to induce apoptosis in cancer cells or tumors.

In certain preferred embodiments, the siRNA targets the sequence in eIF5A1 of 5′-GCT GGA CTC CTC CTA CAC A-3′. siRNA is dsRNA and one strand of the dsRNA comprises the sequence of 5′-GCU GGA CUC CUC CUA CAC A-3′. In certain embodiments the siRNA is stabilized to prevent degradation in serum.

The full length eIF5A1 polynucleotide and/or the eIF5A polynucleotide encoding the truncated eIF5A1 protein may be present in an expression vector. In certain embodiments, the full length eIF5A1 polynucleotide and/or the eIF5A polynucleotide encoding the truncated eIF5A1 protein and/or the siRNA are complexed to polyethylenimine. The full length eIF5A1 polynucleotide and/or the eIF5A polynucleotide encoding the truncated eIF5A1 protein and/or the siRNA are independently complexed to polyethylenimine.

The present invention also provides a method of inducing apoptosis is a mammalian cancer cell or mammalian tumor by providing to the mammal a composition or medicament described herein, for example comprising a nucleotide encoding a truncated eIF5A1, optionally comprising a nucleotide encoding a full length eIF5A or a nucleotide encoding a full length mutant eIF5A and optionally comprising an siRNA targeted against the 3′UTR of eIF5A. In certain embodiments the cancer is multiple myeloma and the composition/medicament is administered intravenously, intra peritoneally or intra tumorally.

The present invention also relates to the combinatorial use of an siRNA targeted against an endogenous gene to knock out or knock down expression of the endogenous gene in a subject and a of a polynucleotide encoding the gene in a delivery vehicle/expression vector provided to the subject to provide expression in the host of the protein encoded by the polynucleotide.

This combination is useful in treating a subject with a disease or condition caused by the existence of a faulty or mutant protein, i.e. where the protein produced in the subject is unable to perform it necessary function or alternatively, fowls up a metabolic pathway or biomolecule interaction because of its faulty structure. The siRNA is designed to target the gene encoding the faulty protein, and knock down or knock out expression of that faulty protein. A polynucleotide encoding a normal (non faulty) protein is administered to the subject and is expressed in the subject so that the normal protein is available to perform its necessary function.

In another embodiment, instead of administering the polynucleotide encoding the desired protein, the protein is administered to the subject. The terms protein, peptide and polypeptide are used herein interchangeably.

The siRNA is preferably designed to target a certain region of the gene so it either knocks down or knocks out endogenous expression of the faulty protein but at the same time will not effect exogenous expression of the administered polynucleotide encoding the normal protein. For example, the siRNA may target the 3′UTR so it does not effect exogenous expression of the administered sense construct (the polynucleotide encoding the protein). By knocking down or knocking out endogenous expression of the faulty gene, there will be less or none of the faulty protein to compete with the normal protein expressed from the exogenous polynucleotide.

One example of a disease state where this application would be useful concerns sickle cell anemia. Sickle cell anemia is a blood disorder that affects hemoglobin, the protein found in red blood cells (RBCs) that helps carry oxygen throughout the body.

Sickle cell anemia occurs when a person inherits two abnormal genes (one from each parent) that results in expression of a mutant hemoglobin (Hbs). The mutant hemoglobin causes the RBCs to change shape. Red blood cells with normal hemoglobin (hemoglobin A, or HbA) move easily through the bloodstream, delivering oxygen to all of the cells of the body. They can easily “squeeze” through even very small blood vessels. Sickle cell anemia occurs because the abnormal form of hemoglobin (HbS) tends to clump together, making red blood cells sticky, stiff, and more fragile, and causing them to form into a curved, sickle shape.

Although several hundred HBB gene variants are known, sickle cell anemia is most commonly caused by the hemoglobin variant HbS. In this variant, the hydrophobic amino acid valine takes the place of hydrophilic glutamic acid at the sixth amino acid position of the HBB polypeptide chain. This substitution creates a hydrophobic spot on the outside of the protein structure that sticks to the hydrophobic region of an adjacent hemoglobin molecule's beta chain. This clumping together (polymerization) of HbS molecules into rigid fibers causes the “sickling” of red blood cells.

Polymerization occurs only after red blood cells have released the oxygen molecules that they carry to various tissues throughout the body. Once red blood cells return to the lungs where hemoglobin can bind oxygen, the long fibers of HbS molecules depolymerize or break apart into single molecules. Cycling between polymerization and depolymerization causes red blood cell membranes to become rigid. The rigidity of these red blood cells and their distorted shape when they are not carrying oxygen can result in blockage of small blood vessels. This blockage can cause episodes of pain and can damage organs.

Sickle cell anemia is an autosomal recessive genetic disorder. For the disease to be expressed, a person must inherit either two copies of HbS variant or one copy of HbS and one copy of another variant. Carriers, who have one copy of the normal HBB gene (HbA) and one copy of HbS, are described as having sickle cell trait and do not express disease symptoms.

Thus, one embodiment of the present invention provides a method of treating subjects with sickle cell anemia. siRNA targeted to the HBB gene is administered to the patient. The siRNA is designed to knock down and preferably knock out the expression of the Hbs variant of hemoglobin. A polynucleotide encoding a normal hemoglobin is provided to the subject so the subject expresses a normal hemoglobin. The siRNA is also designed so that it will not interfere with expression of the exogenous polynucleotides encoding the normal hemoglobin. Thus, the subject no longer makes the variant hemoglobin (or makes substantially less) and instead makes normal healthy hemoglobin, resulting in more normal red blood cells, which function normally.

The present invention is also useful in situations where a post translational modification occurs to the protein, which causes or leads to a disease state. siRNA is used to knock down expression of the endogenous protein so none or less is available for the post translational modification. Then, a polynucleotide encoding a protein is provided to the patient for exogenous expression. The protein is modified so that it is unable to be post translationally modified. This protein is then available to the body for its appropriate use, but will not lead to the disease state because it is not able to be post translationally modified. One skilled in the art would understand different post translational modifications. For example, after translation, the posttranslational modification of amino acids extends the range of functions of the protein by attaching to it other biochemical functional groups such as acetate, phosphate, various lipids and carbohydrates, by changing the chemical nature of an amino acid (e.g. citrullination) or by making structural changes, like the formation of disulfide bridges. Also, enzymes may remove amino acids from the amino end of the protein, or cut the peptide chain in the middle. For instance, the peptide hormone insulin is cut twice after disulfide bonds are formed, and a propeptide is removed from the middle of the chain; the resulting protein consists of two polypeptide chains connected by disulfide bonds. Also, most nascent polypeptides start with the amino acid methionine because the “start” codon on mRNA also codes for this amino acid. This amino acid is usually taken off during post-translational modification. Other modifications, like phosphorylation, are part of common mechanisms for controlling the behavior of a protein, for instance activating or inactivating an enzyme. Another post translational modification includes the hypusination of eukarotic initiation factor 5A (eIF5A) by deoxyhypusine synthase (DHS).

Thus, the invention provides a method of altering expression of a gene in a subject, wherein a polynucleotide encoding a protein is provided to a patient and is expressed in the patient. The protein may be a normal/wild type protein or a mutated protein. Expression of the corresponding endogenous gene is suppressed with the siRNA that is administered to the subject.

The method further comprises providing a construct comprising a polynucleotide encoding the target protein wherein the polynucleotide is expressed in the subject to produce the target protein. In certain embodiments where the endogenous gene expresses a faulty protein, the polynucleotide is designed to encode either a normal/healthy protein. The siRNA is administered to suppress expression of the faulty endogenous protein. In certain embodiments where the endogenous gene expresses a normal healthy protein, the polynucleotide is designed to encode a mutant protein that can not be postranslationally modified as would occur with a normal/healthy or non mutant protein. The siRNA is administered to suppress expression of the endogenous protein so there is less of this protein to be available for posttranslational modification.

In certain embodiments, the siRNA is chosen or designed to target regions of the gene so as to not effect expression of the exogenous polynucleotide. For example, the siRNA may target the 3′ UTR or 3′ end.

The siRNA may be delivered to the patient as either naked siRNA or naked siRNA stabilized for serum. The siRNA may by either injected systemically, i.e. IP or IV. Alternatively, the siRNA may be injected or delivered locally to the desired area of the body. In certain embodiments, the siRNA may be administered in a delivery vehicle such as but not limited to dendrimers, liposomes, or polymers.

The polynucleotides encoding the desired protein may be administered through any delivery means that provide or allow expression of the nucleotide. The term polynucleotide and nucleotide are used herein interchangeably. Delivery may be through any viral or non-viral mechanism, such as but not limited to plasmids, expression vectors, viral constructs, adenovirus constructs, dendrimers, liposomes, or polymers.

In certain embodiments an expression plasmid having reduced CpG dinucleotides is used to express the polynucleotides. Any promoter capable of promoting expression of the polynucleotide may be used, which may be chosen based on the application desired for the therapy. For example, for killing multiple myeloma, a promoter specific for B cells may be desirable, such as human B29 promoter/enhancer. In other embodiments, the promoter may be another tissue specific promoter, or may be a system promoter.

The polynucleotides encoding the target protein may be delivered through IV or subcutaneous injection or any other biologically suitable delivery mechanism.

Alternatively, the polynucleotides may be delivered in liposomes or any other suitable “carrier” or “vehicle” that provides for delivery of the DNA (or plasmid or expression vector) to the target tumor or cancer cells. See for example, Luo, Dan, et al., Nature Biotechnology, Vol. 18, January 2000, pp. 33-37 for a review of synthetic DNA delivery systems. Thus, it may be preferable to deliver the nucleotides/plasmid/expression vector via a vehicle of nanometer size such as liposomes, dendrimers or a similar non-toxic nano-particle. The vehicle preferably protects the nucleotides/plasmid/expression vector from premature clearance or from causing an immune response while delivering an effective amount of the nucleotides/plasmid/expression vector to the subject, tumor or cancer cells. Exemplary vehicles may range from a simple nano-particle associated with the nucleotides/plasmid/expression vector to a more complex pegylated vehicle such as a pegylated liposome having a ligand attached to its surface to target a specific cell receptor.

Liposomes and pegylated liposomes are known in the art. In conventional liposomes, the molecules to be delivered (i.e. small drugs, proteins, nucleotides or plasmids) are contained within the central cavity of the liposome. One skilled in the art would appreciate that there are also “stealth,” targeted, and cationic liposomes useful for molecule delivery. See for example, Hortobagyi, Gabriel N., et al., J. Clinical Oncology, Vol. 19, Issue 14 (July) 2001:3422-3433 and Yu, Wei, et al., Nucleic Acids Research. 2004, 32(5); e48. Liposomes can be injected intravenously and can be modified to render their surface more hydrophilic (by adding polyethylene glycol (“pegylated”) to the bilayer, which increases their circulation time in the bloodstream. These are known as “stealth” liposomes and are especially useful as carriers for hydrophilic (water soluble) anticancer drugs such as doxorubicin and mitoxantrone. To further the specific binding properties of a drug carrying liposome to a target cell, such as a tumor cell, specific molecules such as antibodies, proteins, peptides, etc. may be attached on the liposome surface. For example, antibodies to receptors present on cancer cells maybe used to target the liposome to the cancer cell. In the case of targeting multiple myeloma, folate, 11-6 or transferrin for example, may be used to target the liposomes to multiple myeloma cells.

Dendrimers are also known in the art and provide a preferable delivery vehicle. See for example Marjoros, Istvan, J., et al, “PAMAM Dendrimer-Based Multifunctional Conjugate for Cancer Therapy: Synthesis, Characterization, and Functionality,” Biomacromolecules, Vol. 7, No. 2, 2006; 572-579, and Majoros, Istvan J., et al., J. Med. Chem, 2005. 48, 5892-5899 for a discussion of dendrimers.

In a preferred embodiment, the delivery vehicle comprises a polyethylenimine nanoparticle. An exemplary polyethylenimine nanoparticle is the in vivo-jetPEI™, currently produced by Polyplus Transfection, Inc. In vivo-jetPEI™ is cationic polymer transfection agent useful as a DNA and siRNA delivery agent. In vivo-jetPEI™ from Polyplus Transfection is a linear polyethylenimine reagent that provides reliable nucleic acid delivery in animals. It is used for gene therapy (Ohana et al., 2004. Gene Ther Mol Bio 8:181-192; Vernejoul et al., 2002. Cancer Research 62:6124-31), RNA interference, (Urbain-Klein et al., 2004. Gene therapy 23:1-6; Grezelinski et al., 2006. Human Gene Therapy 17:751-66), and genetic vaccination (Garzon et al., 2005. Vaccine 23:1384-92). In vivo JET-PEI is currently in use in human clinical trials as a delivery vector for cancer gene therapy (Lemkine et al., 2002. Mol. Cell. Neurosci. 19:165-174).

In vivo-jetPEI™ condenses nucleic acids into roughly 50 nm nanoparticles, which are stable for several hours. As a result of this unique protection mechanism, aggregation of blood cells following injection is reduced compared to other reagents thereby preventing restricted diffusion within a tissue, erythrocyte aggregation and microembolia. These nanoparticles are sufficiently small to diffuse into the tissues and enter the cells by endocytosis. In vivo-jetPEI™ favors nucleic acids release from the endosome and transfer across of the nuclear membrane.

In a preferred embodiment, both the siRNA and a vector/plasmid comprising the polynucleotide are administered to the subject via an in vivo-jetPEI™ complex. The siRNA and the vector/plasmid comprising the polynucleotide maybe complexed together via a polymer complex such as polyethylenimine or the in vivo jetPEI™ complex or may separately complexed to a polymer. For instance, where the siRNA and the vector/plasmid comprising the polynucleotide are to be administered separately to the subject (separately in the meaning of time and/or delivery site) it is preferable to have the siRNA and the polynucleotide complexed to a different carrier. Where the administration will occur at the same time and at the same site, it may be preferable to complex the siRNA and the polynucleotide together.

In another embodiment, instead of a plasmid or vector being administered to deliver a polynucleotide that will be expressed in the subject, the protein per se is delivered to the subject. The protein may be either isolated or may be synthetic.

One embodiment of the present invention provides a method of treating cancer in a subject, including mammals and humans. Treating cancer includes, but is not limited to inducing apoptosis in cancer cells, killing cancer cells, reducing the number of cancer cells and reducing tumor volume/weight. The method comprises administering a composition comprising eIF5A1 siRNA and a polynucleotide encoding a mutant eIF5A1. The composition and eIF5A1 siRNA and a polynucleotide encoding a mutant eIF5A1 are discussed herein below.

All cells produce eukaryotic initiation factor 5A (“eIF-5A”) (or also referred to herein as “factor 5A”). Mammalian cells produce two isoforms of eIF-5A1 (eIF-5A1 and eIF-5A2). eIF-5A1 has been referred to as apoptosis-specific eIF-5A, as it is upregulated in cells undergoing apoptosis. Human eIF-5A1 has the accession number NM 001970 and is shown in FIG. 1. It is believed that eIF-5A1 is responsible for shuttling out of the nucleus subsets of mRNAs encoding proteins necessary for apoptosis. eIF-5A2 has been referred to as proliferation eIF-5A as it is believed to be responsible for shuttling out of the nucleus subsets of mRNAs encoding proteins necessary for cellular proliferation. See Liu & Tartakoff (1997) Supplement to Molecular Biology of the Cell, 8, 426a. Abstract No. 2476, 37th American Society for Cell Biology Annual Meeting, and Rosorius et al. (1999) J. Cell Science, 112, 2369-2380.

Both factor 5As are post translationally modified by deoxyhypusine synthase (“DHS”). DHS hypusinates the eIF-5As. Hypusine, a unique amino acid, is found in all examined eukaryotes and archaebacteria, but not in eubacteria, and eIF-5A is the only known hypusine-containing protein. Park (1988) J. Biol. Chem., 263, 7447-7449; Schumann & Klink (1989) System. Appl. Microbiol., 11, 103-107; Bartig et al. (1990) System. Appl. Microbiol., 13, 112-116; Gordon et al. (1987a) J. Biol. Chem., 262, 16585-16589. Hypusinated eIF-5A is formed in two post-translational steps: the first step is the formation of a deoxyhypusine residue by the transfer of the 4-aminobutyl moiety of spermidine to the a-amino group of a specific lysine of the precursor eIF-5A catalyzed by deoxyhypusine synthase. The second step involves the hydroxylation of this 4-aminobutyl moiety by deoxyhypusine hydroxylase to form hypusine.

The amino acid sequence of eIF-5A is well conserved between species, and there is strict conservation of the amino acid sequence surrounding the hypusine residue in eIF-5A, which suggests that this modification may be important for survival. Park et al. (1993) Biofactors, 4, 95-104. This assumption is further supported by the observation that inactivation of both isoforms of eIF-5A found to date in yeast, or inactivation of the DHS gene, which catalyzes the first step in their activation, blocks cell division. Schnier et al. (1991) Mol. Cell. Biol., 11, 3105-3114; Sasaki et al. (1996) FEBS Lett., 384, 151-154; Park et al. (1998) J. Biol. Chem., 273, 1677-1683. However, depletion of eIF-5A protein in yeast resulted in only a small decrease in total protein synthesis suggesting that eIF-5A may be required for the translation of specific subsets of mRNA's rather than for protein global synthesis. Kang et al. (1993), “Effect of initiation factor eIF-5A depletion on cell proliferation and protein synthesis,” in Tuite, M. (ed.), Protein Synthesis and Targeting in Yeast, NATO Series H. The recent finding that ligands binding eIF-5A share highly conserved motifs also supports the importance of eIF-5A. Xu & Chen (2001) J. Biol. Chem., 276, 2555-2561. In addition, the hypusine residue of modified eIF-5A was found to be essential for sequence-specific binding to RNA, and binding did not provide protection from ribonucleases.

The present inventors have shown that when polynucleotides encoding eIF-5A are administered to cells, there is an increase in apoptosis those cells. They have shown that they have been able to push cancer cells into apoptosis by administering eIF-5A1 polynucleotides that are then expressed in the cancer cells. See co-pending application Ser. Nos. 10/200,148; 11/287,460; 11/293,391 and 11/637,835, all of which are incorporated by reference in their entireties.

The present inventors have additionally determined that when cells have a build up of the hypusinated form of factor 5A, the cells enter into a survival mode and do not undergo apoptosis as they normally would over time. Notably, in cancer cells, there is a significant amount of hypusinated factor 5A and thus, the cells do not enter into apoptosis (and do not die). Thus, to treat cancer by killing the cancer cells (push the cancer cells to enter into the apoptosis pathway), a polynucleotide encoding eIF-5A1 is administered to the subject or to the cancer cells or tumor to provide increased expression of eIF-5A1, which in turn causes apoptosis in the cancer cells and ultimately cell death and tumor shrinkage. However, if one were to only provide polynucleotides encoding the eIF-5A1 protein to up regulate gene expression of eIF-5A1 and not also use siRNA to knock down endogenous expression of eIF-5A1, there is a tug of war: the eIF-5A1 expression directing the cells towards the apoptosis pathway competes with the presence of the hypusinated factor 5A directing the cells towards the cell survival pathway. The present invention eliminates this tug of war and represents an improvement over only increasing expression of eIF-5A1. The polynucleotides administered to the subject or cell are mutated so that the resulting expressed protein can not be hypusinated. In addition endogenous expression of factor 5A is knocked out/down with siRNA targeted against eIF-5A so there is none/less endogenous eIF-5A1 around to by hypusinated. Thus, since there is no (or substantially less) hypusinated eIF-5A in the cells, they are not pushed into survival mode.

The polynucleotide encoding a mutated eIF-5A1 is preferably mutated so that it can not be hypusinated and thus will not be available to drive the cell into survival mode.

For example, in one embodiment, the polynucleotide encoding eIF-5A is mutated to so that the lysine (K) at position 50, which is normally hypusinated by DHS, is changed to an alanine (A) (which can not be hypusinated). This mutant is denoted as K50A.

In another embodiment, the lysine at position 67 is changed to an arginine (R). This mutant is denoted as (K67R). In another embodiment the lysine (K) at position 67 is changed to an alanine (A) and is denoted as (K67A). In another embodiment, the lysine (K) at position 50 is changed to an arginine (K50R) and another embodiment provides a mutant where the lysine (K) at position 47 is changed to an arginine (K47R).

In other embodiments, a double mutant is used. One double mutant is where the lysine (K) at position 50 is changed to an arginine (R) and the lysine (K) at position 67 is changed to a arginine (R). This double mutant is referred to as KSOR/K67R. This double mutant is similarly unable to be hypusinated but the changes in the amino acids do not alter the 3-D structure of eIF-5A1 as much as the single mutation (K50A). The double mutation thus provides a protein that is very similar in 3-D shape and folding as the wild type and thus is more stable than the single mutant. Being more stable, it exists longer in the body to provide longer therapeutic benefit. Thus, the body will have the factor 5A it needs for normal cell function but it will not be able to hypusinated so the cells do not get locked into the cell survival mode and escape apoptosis.

Another double mutant is where the lysine (K) at position 47 is changed to an arginine (R) and the lysine at position 50 is changed to an arginine (R). This mutant is denoted as (K47R/K50R). The invention provides another double mutant where the lysine (L) at position 50 is changes to an alanine (A) and the lysine at position 67 is changes to an alanine (A). This mutant is denoted as (K50A/K67A).

Because the body needs factor 5A for normal cell survival and healthy cell proliferation, it is preferable not to shut off expression completely in the subject with the siRNA, if the siRNA is delivered systemically. Control of eIF-5A expression can be achieved by either using an siRNA that is not as good at shutting off expression (i.e. shuts down or reduces expression but does not completely shut off expression) or alternatively, or utilizing a dosing and/or treatment regimen to balance expression levels to allow normal growth and functioning of healthy cells but also to push cancerous cells to apoptosis.

Alternatively, one may utilize local delivery of siRNA. If the siRNA is delivered locally to the cancer cell or tumor, then the expression is preferably knocked out. By knocking out expression, there is no factor 5A around that can be hypusinated and thus there is no hypusinated eIF-5A to lock the cells into survival mode. Since the siRNA is delivered locally to the cancer or tumor, there is no need to have eIF-5A available for regular cell growth.

In certain embodiments, the endogenous gene is eIF5A1. siRNA targeted against eIF5A1 is administered to the subject to suppress expression of the endogenous eIF-5A1. In certain embodiments the siRNA comprises SEQ ID NO:1 or SEQ ID NO:2 or is any siRNA targeted against eIF5A1 that will suppress expression of endogenous eIF-5A1. In certain embodiments, the eIF5A1 is human eIF-5A1 (shown in FIG. 1) and the subject is a human. Other siRNAs targeted against human eIF-5A1 are known and disclosed in co-pending application Ser. Nos. 11/134,445; 11/287,460; 11/184,982; 11/293,391; 11/725,520; 11/725,470; 11/637,835. In other embodiments, the subject is a mammal and the eIF5A1 is specific to the mammal. For example, the subject is a dog and the eIF5A1 is canine eIF5A1. In certain embodiments, the siRNA consists essentially of the siRNA construct shown in FIG. 25. For example, the siRNA contains nucleic acids targeted against the eIF5A1 but also contains overhangs such as U or T nucleic acids or also contains tags, such as a his tag (often referred to as HA tag—which is often used in in vitro studies). Molecules or additional nucleic acids attached at either the 5′ or 3′ end (or even within the consecutive string of nucleic acids shown in FIG. 25, for example) may be included and fall within the “consisting essentially of as long as the siRNA construct is able to reduce expression of the target gene. Preferably the siRNA targets regions of the eIF5A1 gene so as to not effect expression of the exogenous polynucleotide. For example the eIF5A1 siRNA targets the 3′ UTR or the 3′ end. The siRNA shown in FIG. 25 an exemplary eIF5A1 siRNA.

The polynucleotide encodes eIF5A1 wherein the polynucleotide is mutated to encode an eIF5A1 variant. The mutated eIF5A1 is designed so that the variant eIF5A1 can not be post translationally modified (can not be hypusinated). Exemplary mutants are discussed herein above.

In the case of cancer involving solid tumors, it may be desirable to deliver the siRNA directly to the tumor. The siRNA maybe administered separately with respect to time as well as the delivery site from the polynucleotide or may administered together at the same time and/or at the same delivery site. One skilled in the art would understand that the timing of administration of the siRNA may be necessarily administered when the endogenous protein is being translated and not after it is already made.

Although the present inventors have earlier shown that eIF5A1 is non toxic to normal tissue (see pending application Ser. No. 11/293,391, filed Nov. 28, 2005, which is incorporated herein by reference in its entirety), a delivery complex (as compared to direct administration of the eIF5A polynucleotides/plasmid/expression vector) may be preferred. A preferred delivery system provides an effective amount of eIF5A1 to the subject, tumor or group of cancer cells, as well as preferably provides a targeted delivery to the tumor or group of cancer cells. Thus, in certain embodiments, it is preferable to deliver the eIF5A1 nucleotides/plasmid/expression vector via a vehicle of nanometer size such as liposomes, dendrimers or a similar non-toxic nano-particle such as a polyethylenimine polymer (such as an in vivo JetPEI™ complex).

The eIF5A1 protein may also be delivered directly to the site of the tumor. One skilled in the art would be able to determine the dose and length of treatment regimen for delivery of eIF5A1 protein.

The molecular basis for the induction of apoptosis by eIF5A1 is discussed below.

Death Receptor Signaling

Treatment of cancer cells with Ad-eIF5A1 (adenovirus with a wild type eIF5A1) or Ad-eIF5A1(K50A) induces activation of caspase 8, which is initiated by death receptor—ligand binding, and caspase 3, the executioner caspase. These are likely to be indirect effects of eIF5A1, and the fact that caspase 8 and caspase 3 are also activated following treatment with eIF5A1(K50A), which cannot be hypusinated, indicates that the effect is attributable to lysine₅₀ eIF5A1. Treatment with Ad-eIF5A1 also appears to result in up-regulation of death receptors as shown previously with upregulation of TNFR1.

Mitochondria′ Pathway

Direct or indirect involvement of lysine₅₀ eIF5A1 in the mitochondrial pathway for apoptosis is supported by a number of observations including the finding that caspase 9 is activated by treatment of cancer cells with either eIF5A1 or

eIF5A1(K50A). As well, p53, which plays a role in activation of the mitochondrial apoptotic pathway, appears to be regulated by eIF5A1. For example, treatment of cancer cells with Actinomycin D up-regulates p53, and this up-regulation of p53 is inhibited by eIF5A1 siRNA. Consistent with this, treatment of cancer cells with Ad-eIF5A1 up-regulates p53 mRNA. Treatment of cancer cells with eIF5A1 also induces migration of Bax from the cytosol to mitochondria, ensuing loss of mitochondrial membrane potential and release of cytochrome C from the intra-mitochondrial space into the cytosol. In addition, this treatment results in up-regulation of cleaved Bc12, Bim and spliced Bim, which are all pro-apoptotic.

MAPK Signaling

In addition, the present inventors have obtained evidence for the involvement of eIF5A1 in MAPK signaling related to apoptosis. For example, treatment of cancer cells with Ad-eIF5A1 up-regulated P-.INK, which in turn inhibits anti-apoptotic Bc12. In addition Ad-eIF5A1 and Ad-eIF5A1(K50A) both induce the formation of P-p38, which can in turn initiate apoptosis by impacting a variety of pro-apoptotic agents including TNFR1 & TNF; FAS & FASL; caspase 8; Bid; Cytochrome C and Capase 3.

NE-κB Signaling

There is evidence that NF-κB signaling supports myeloma growth. For example, myeloma cell adhesion to bone marrow stromal cells induces NF-κB—dependent transcriptional up-regulation of IL-6, which is both a growth and anti-apoptotic factor in multiple myeoloma [Chauhan et al. (1996) Blood 87, 1104.] In addition, TNF-α secreted by myeloma cells activates NF-κB in bone marrow stromal cells, thereby up-regulating IL-6 transcription and secretion. TNF-a also activates NF-κB in myeloma cells resulting in up-regulation of the intracellular adhesion molecule-1 (ICAM-1; CD54) and the vascular cell adhesion molecule-1 (VCAM-1; CD106) on both myeloma cells and bone marrow stromal cells [Hideshima et al. (2001) Oncogene 20,4519]. This in turn enhances the association of myeloma cells with bone marrow stromal cells [Hideshima et al. (2001) Oncogene 20,4519]. Conversely, these effects are inhibited by blocking TNFα-induced NF-κB activation [Hideshima et al. (2001) Oncogene 20,4519]. Indeed, it seems likely that NF-κB mediates protection against TNFa-induced apoptosis in myeloma cells [Hideshima et al. (2002) JBC 277, 16639]. These and other observations have prompted the view that NF-kB signaling may be an attractive target for multiple myeloma therapies.

The inventors have shown that eIF5A1 siRNA inhibits both the activation of NF-κB and the formation of ICAM-1 in human myeloma cells. These observations indicate that eIF5A1 plays a role in NF-κB activation, and inasmuch as the ensuing effects of NF-κB activation are pro-survival in nature, we predict that this activation is mediated, directly or indirectly, by hypusinated eIF5A1.

IL-1

Over-production of the pro-inflammatory cytokine, IL-1, by myeloma cells is a characteristic feature of multiple myeloma that leads to deterioration of bone tissue. eIF5A1 siRNA has been shown to dramatically reduce the overproduction of IL-1 induced by an LPS challenge in mice.

One embodiment of the present invention provides a method of treating multiple myeloma. Multiple myeloma (“MM”) is a progressive and fatal disease characterized by the expansion of malignant plasma cells in the bone marrow and by the presence of osteolytic lesions. Multiple myeloma is an incurable but treatable cancer of the plasma cell. Plasma cells are an important part of the immune system, producing immunoglobulins (antibodies) that help fight infection and disease. Multiple myeloma is characterized by excessive numbers of abnormal plasma cells in the bone marrow and overproduction of intact monoclonal immunoglobulins (IgG, IgA, IgD, or IgE; “M-proteins”) or Bence-Jones protein (free monoclonal light chains). Hypocalcaemia, anemia, renal damage, increased susceptibility to bacterial infection, and impaired production of normal immunoglobulin are common clinical manifestations of multiple myeloma. Multiple myeloma is often also characterized by diffuse osteoporosis, usually in the pelvis, spine, ribs, and skull.

The present invention seems to be well suited to treat multiple myeloma because of the stimulation feedback loop found in multiple myeloma. For instance, multiple myeloma produces I1-1 in low concentrations in bone marrow. The I1-1 in turn stimulates stromal cells to produce IL-6, which then goes onto stimulate growth of the multiple myeloma. The inventors have previously shown (see pending application Ser. Nos. 11/725,539 and 11/184,982) that siRNA directed against eIF-5A1 was able to inhibit expression of proinflammatory cytokines, such as I1-1; TNF-α, and 11-8). Thus, the siRNA would not only knock down expression of eIF-5A so less is available for hypusination, it would also cut off or decrease the 11-1/11-6 feedback loop.

An siRNA targeting human eIF5A was used to suppress levels of endogenous hypusinated eIF5A in tumors, while an RNAi-resistant plasmid expressing a mutant of eIF5A (eIF5A1^K50R), that is incapable of being hypusinated, was used to raise the levels of unmodified eIF5A in vivo. Intra-tumoral injection of PEI nanocomplexes containing eIF5A siRNA inhibited MM tumor growth by more than 80% (*** p=0.0003) versus complexes containing a control siRNA, indicating that suppressing levels of hypusinated eIF5A has an anti-tumoral effect. PEI complexes containing an eIF5A^K50R expression plasmid had a similar effect and inhibited tumor growth by more than 70% (**=p 0.001) versus complexes containing a control plasmid. Thus, MM tumor growth can be inhibited either by suppression of the growth-promoting hypusinated eIF5A or by increasing levels of the pro-apoptotic unhypusinated form of eIF5A. Intra-tumoral delivery of complexes containing both eIF5A siRNA and RNAi-resistant eIF5A1(5° R plasmid had a synergistic effect on tumor growth and resulted in significant tumor shrinkage, inhibiting tumor growth by 94% (*** p=0.0002). Intra-venous delivery of eIF5A siRNA/eIF5A^K50R PEI complexes also efficiently reduced tumor growth by 95% (** p=0.002) indicating systemic delivery of the therapeutic is feasible.

Both local and systemic delivery of eIF5A siRNA/eIF5A^K50R pDNA PEI complexes resulted in a significant anti-tumoral response in multiple myeloma.

The present invention further provides a composition useful in the treatment of cancer, including multiple myeloma. In a preferred embodiment, the composition is a complex of a plasmid DNA encoding point-mutated eIF5A1 that cannot be hypusinated and eIF5A1 siRNA that selectively suppresses endogenous human eIF5A1 but has no effect on the point-mutated eIF5A1 encoded by the plasmid. eIF5A1 siRNAs and polynucleotides encoding mutant eIF5A1 are discussed above. The plasmid DNA and the siRNA are both preferably complexed to PEI (polyethylenimine) nanoparticles. They may be complexed separately and administered separately or together or they may be complexed together. The DNA and the RNA bind to positively charged amino groups on the PEI and are released when the nanoparticles are taken up into cells. It has been demonstrated that PEI-nucleic acid complexes are effectively taken up into both dividing and non-dividing cells.

The plasmid DNA preferably encodes eIF5A1(K50R) which, like eIF5A1(K50A), cannot be hypusinated and, accordingly, is strongly apoptogenic. The expression of eIF5A1(K50R) is preferably regulated by a B-cell-specific promoter.

The eIF5A1 siRNA is preferably specific to the 3′-end of endogenous human eIF5A1 and has no effect on expression of the trans eIF5A1(K50R). An exemplary preferred eIF5A1 siRNA comprises, consists essentially of or consists of the siRNA shown in FIG. 25. The rationale for including the eIF5A1 siRNA is: (1) to deplete endogenous eIF5A1, which is almost all hypusinated and hence in the pro-survival form; (2) to inhibit activation of NF-κB, and thereby reduce the production of IL-6 and the formation of intracellular adhesion molecules; and (3) to inhibit the formation of IL-1. That eIF5A1 siRNA acts synergistically with eIF5A1(K50R) to induce apoptosis in myeloma cells. Inasmuch as (2) and (3) above are pro-survival events, they are likely mediated by hypusinated eIF5A1, and hence not affected by eIF5A1(K50R) which cannot by hypusinated. This approach results in a larger pool of unhypusinated eIF5A leading to apoptosis of cancer cells, including multiple myeloma cells, with little effect on healthy cells.

A preferred composition is referred to herein as SNS01. SNSOI is a complex containing both, an RNAi-resistant plasmid DNA encoding eIF5A^K50R driven by a promoter that restricts expression to cells of B-cell origin (including myeloma cells) for enhanced safety, and an siRNA targeting human eIF5A with dTdT 3′ overhangs for enhanced nuclease resistance and which the siRNA and the plasmid are complexed to in vivo JetPEI™

EXAMPLES

Example 1

Transfection of HeLaS3 Cells with Wild Type and Variants of eIF-5A1

HeLa S3 cells were transfected using Lipofectamine 2000 with plasmids expressing HA-tagged eIF5A1 variants including wild-type eIF5A1 (WT), eIF5A1K50R (K50R), eIF5A1K67R (K67R), eIF5A1K67A (K67A), eIF5A1K47R/K50R (K4750R), eIF5A1K50R/K67R (K5067R), or eIF5A1K50A/K67A (K5067A). A plasmid expressing LacZ was used as a control. At 24 and 48 hours (A) or 28 and 52 hours (B) after transfection, the cell lysate was harvested and fractionated by SDS-PAGE. Expression levels of transfected eIF5A1 was detected using an antibody against HA. Result: Mutation of eIF5A1 at a lysine in the putative ubiquination site (K67R) increased the accumulation of the eIF5A1 transgene above wild-type (A). Mutation of eIF5A1 at the lysine required for hypusination (K50R) also increased accumulation of eIF5A1 transgene above wild-type eIF5A1 (B). A double mutant form of eIF5A1 (K50A/K67A) was expressed particularly well when compared to the unmutated wild-type eIF5A1 transgene (A+B). FIGS. 2A and 2B.

Example 2

Transfection of KAS Cells with Wild Type and Variants of eIF-5A1

KAS cells were transfected using PAMAM dendrimer (FMD44) with plasmids expressing HA-tagged eIF5A1 variants including wild-type eIF5A1 (5A1), eIF5A1K67A (K67A), eIF5A1K50A/K67A (K50A K67A), eIF5A1K50R (K50R), eIF5A1K47R (K47R), eIF5A1K67R (K67R), eIF5A1K47R/K50R (K47R K50R),or eIF5A1K50R/K67R (K50R K67R). A plasmid expressing LacZ was used as a control. 48 hours (after transfection, the cell lysate was harvested and fractionated by SDS-PAGE. Expression levels of transfected eIF5A1 was detected using an antibody against HA. Equal loading was verified using an antibody against actin. Result: Mutation of eIF5A1 at a lysine in the putative ubiquination site (K67A or K67R) increased the accumulation of the eIF5A1 transgene above wild-type. Mutation of eIF5A1 at the lysine required for hypusination (K50R) or at an acetylation site (K47R) also increased accumulation of eIF5A1 transgene above wild-type eIFSA. A double mutant form of eIF5A1 (K50A/K67A) was also expressed at higher levels when compared to the unmutated wild-type eIF5A1 transgene. See FIG. 3.

Example 3

Transfection of KAS Cells Using PAMAM Dendrimer

KAS cells were transfected using PAMAM dendrimer (FMD45-2) with plasmids expressing HA-tagged eIF5A1 variants including eIF5A1K50R (KSOR), eIF5A1K50A/K67A (K50A/K67A), or eIF5A1K50R/K67R (KSOR K67R). A plasmid expressing LacZ was used as a control. Seventy-two hours after transfection, the cells were stained with Annexin/PI and analyzed by FACS. Cells that stained positively for Annexin V and negatively for PI (propidium iodide) were considered to be in the early stages of apoptosis (Ann+/PI−) and cells that stained positively for both Annexin V and PI were considered to be in the late stages of apoptosis (Ann+/PI+). Result: Mutation of eIF5A1 at a lysine in the hypusination site (K50R) or in the putative ubiquination site (K67R), as well as the double mutant (K50A/K67A) resulted in apoptosis of KAS cells significantly above the levels of the LacZ control. See FIG. 4.

Example 4

Transfection of KAS Cells with Plasmids Expressing eIF-5A1 and eIF-5A1 Variants

KAS cells were transfected using Lipofectamine 2000 with plasmids expressing HA-tagged eIF5A1 variants including eIF5A1K50A (K50A), eIF5A1K50R (K50R), eIF5A1K67R (K67R), eIF5A1K50A/K67A (K50A/K67A), or eIF5A1K50R/K67R (K50R K67R). A plasmid expressing LacZ was used as a control. Seventy-two hours after transfection, the cells were stained with Annexin/PI and analyzed by FACS. Cells that stained positively for Annexin V and negatively for PI (propidium iodide) were considered to be in the early stages of apoptosis (Ann+/PI−) and cells that stained positively for both Annexin V and PI were considered to be in the late stages of apoptosis (Ann+/PI+). Result: Mutation of eIF5A1 at a lysine in the hypusination site (K50R) or In the putative ubiquination site (K67R), as well as the double mutant (K50A/K67A) resulted in apoptosis of KAS cells significantly above the levels of the LacZ control. See FIG. 5.

Example 5

The Use of Mutated eIF-5A1 to Treat KAS Cells Results in Apoptosis

KAS cells were transfected using Lipofectamine 2000 with plasmids expressing HA-tagged eIF5A1 variants eIF5A1K50R (K50R) or eIF5A1K50A/K67A (K50A/K67A. A plasmid expressing LacZ was used as a control. Seventy-two hours after transfection, the cells were stained with Annexin/PI and analyzed by FACS. Cells that stained positively for Annexin V and negatively for PI (propidium iodide) were considered to be in the early stages of apoptosis (Ann+/PI−) and cells that stained positively for both Annexin V and PI were considered to be in the late stages of apoptosis (Ann+/PI+). Result: Mutation of eIF5A1 at a lysine in the hypusination site (K50R) or mutation of eIF5A1 at both the hypusination site and in the putative ubiquination site (K50A/K67A) resulted in apoptosis of KAS cells significantly above the levels of the LacZ control. See FIG. 6.

Example 6A

siRNA/Adenovirus-Mediated Killing of Multiple Myeloma Cells

KAS (human multiple myeloma) cells were maintained in S10 media [RPMI 1640 with 4 ng/ml IL-6, 10% fetal bovine serum (FBS), and penicillin/streptomycin (P/S)]. KAS cells were transfected with 58.7 pmoles of siRNA using Lipofectamine 2000 (Invitrogen). Mock transfected cells were treated with Lipofectamine 2000 in the absence of siRNA. Transfection was conducted in the antibiotic-free S10 media.

a) siRNAs targeting human eIF5A1:

• • eIF5A1 siRNA target #1 (the siRNA targets this region of human eIF5A1: 5′-AAGCTGGACTCCTCCTACACA-3′ (SEQ ID NO: ______). The siRNA sequence is shown in FIG. 25 and is often referred to herein as h5A1.
  • eIF5A1 siRNA target #2 eIF5A1 (this siRNA targets this region of human eIF5A1: 5′-AAAGGAATGACTTCCAGCTGA-3′ (SEQ ID NO: ______). (The siRNA sequence is often referred to herein ashSA1-ALT)

b) control siRNA: The control siRNA had the following sequence: sense strand, 5″-ACACAUCCUCCUCAGGUCGdTdT-3′; and antisense strand, 3′-dTdTUGUGUAGGAGGAGUCCAGC-5″.

Other controls that have been used include non-targeting validated siRNAs from Dharmacon since they have been micro-array tested to limit unwanted off-targeting effects. For example, for in vitro work studying NFkB, the control used was Dharmacon's non-targeting siRNA's (sequence D-001700-01) and for in vivo work, the control used was Dharmacorfs (sequence D-001810-01).

Four hours after transfection, the cells were pelleted and resuspended in 1 ml of S10 media. Seventy-two hours after the initial siRNA transfection, the transfected KAS cells were counted and seeded at 300,000 cells/well in a 24-well plate and transfected with the same siRNA a second time.

Four hours after transfection, the cells were pelleted and resuspended in 1 ml of S10 media (without IL-6) containing 3000 ifu of either Ad-LacZ (Adenovirus expressing-galactosidase) or Ad-5A1M (Adenovirus expressing human eIF5A1^K50A).

Seventy-two hours later the cells were harvested and analyzed for apoptosis by staining with Annexin V-FITC and PI (BD Bioscience) followed by FACS analysis.

• • a) early apoptosis was defined as cells that were positively stained with Annexin-FITC and negative for PI-staining (Ann+/PI−)
  • b) total apoptosis was defined as the total of cells either in early apoptosis (Ann+/PI−) or late apoptosis/necrosis (Ann+/PI+)

The 5A1 siRNA targeting #1 targets the 3′UTR of human eIF5A1 and therefore will not affect expression of eIF5A1 from adenovirus. 5A1 siRNA targeting #2 targets within the open reading frame of human eIF5A1 and so it could potentially interfere with expression of eIF5A1 from the adenovirus.

Results:

Cells treated with siRNA and infected with adenovirus expressing the eIF-5A1 K50A variant undergo apoptosis in greater numbers than non-treated cells and cells treated only with siRNA. See FIG. 7.

Example 6B

Pre-Treatment with eIF5A1 siRNA Against eIF5A1 Target #1 (Shown in FIG. 25), Reduced Expression of Endogenous eIF5A1 but Allows Accumulation of RNAi-Resistant eIF5A1^K50A Expressed by Adenovirus

KAS cells were transfected using Lipofectamine 2000 with either a control siRNA (C) or one of two siRNAs targeting eIF5A1 (#1 and #2). The eIF5A1 siRNA #1 targets the 3′UTR of eIF5A1 and therefore does not interfere with expression of eIF5A1 from adenovirus since it contains only the open reading frame of eIF5A1. The sequence of the siRNA is shown in FIG. 25. The eIF5A1 #2 siRNA targets the open reading frame of eIF5A1 and will therefore affect expression of both endogenous and exogenously-expressed eIF5A1. Seventy-two hours after the initial transfection hours the cells were transfected with the same siRNA a second time. Four hours later the transfection complexes were removed from the cells and replaced with growth media (−) IL6 containing either Ad-LacZ (L) or Ad-eIF5A1^K50A (5M). Seventy-two hours later the cell lysate was harvested and analyzed by Western blot using antibodies against eIFSA and actin. See FIG. 7B. Accumulation of virally expressed eIF5A1 can be observed (lane 1 vs lane 2) and reduction of eIFSA expression by eIF5A1 siRNAs targeting #1 and #2 can be clearly seen (lanes 5 and 7 vs lane 3). As expected, the eIF5A1 siRNA #1 does not affect accumulation of the virally expressed eIF5A1^K50A (lane 6 vs lane 4) while the eIF5A1 siRNA #2 only moderately affects expression of the virally-expressed transgene (lane 8 vs lane 4).

Example 6C

Pre-Treatment with eIF5A1 siRNA Against Target #1 Prior to Adenovirus Infection Reduces Expression of Phosphorylated NF-κB in Human Multiple Myeloma Cells

KAS cells were transfected using Lipofectamine 2000 with either a control siRNA (hC) or an siRNA targeting eIF5A1 (#1). The eIF5A1 siRNA #1 targets the 3′UTR of eIF5A1 and will therefore not interfere with expression of eIF5A1 from adenovirus since it contains only the open reading frame of eIF5A1. Seventy-two hours after the initial transfection hours the cells were transfected with the same siRNA a second time. Four hours later the transfection complexes were removed from the cells and replaced with growth media (+) IL6 containing either Ad-LacZ (L) or Ad-eIF5A1^K50A (5M). Twenty-four hours later the cell lysate was harvested and analyzed by Western blot using antibodies against phospho-NF-kB p65 (Ser 536) and eIF5A. As expected, the eIF5A1 siRNA #1 does not affect accumulation of the virally expressed eIF5A1^K50A. Phosphorylation of NF-kB p65 at serine 536 regulates activation, nuclear localization, protein-protein interactions, and transcriptional activity. See FIG. 7C.

Example 6D

Pre-Treatment with eIF5A1 siRNA #1 Prior to Adenovirus Infection Reduces Expression of Phosphorylated NF-kB and ICAM-1 in Human Multiple Myeloma Cells

KAS cells were transfected using Lipofectamine 2000 with either a control siRNA (C) or one of two siRNAs targeting eIF5A1 (#1 and #2). Seventy-two hours after the initial transfection hours the cells were transfected with the same siRNA a second time. Four hours later the transfection complexes were removed from the cells and replaced with growth media (+) IL6. Twenty-four hours after the second transfection, the cells were stimulated with 40 ng/ml TNF-a and cell lysate was harvested at 0, 4, or 24 hours and analyzed by Western blot using antibodies against phospho-NF-kB p65 (Ser 536), ICAM-1 and actin. A reduction in TNF-a induced NF-kB p65 phosphorylation (ser 536) and ICAM-1 expression was observed following transfection with both eIF5A1-specific siRNAs. Phosphorylation of NF-kB p65 at serine 536 regulates activation, nuclear localization, protein-protein interactions, and transcriptional activity. ICAM-1 is an inter-cellular adhesion surface glycoprotein that is believed to be involved in the pathogenesis of multiple myeloma. See FIG. 7D.

Example 6E

Pretreatment of KAS Cells with siRNA Increases Apoptosis by eIF5A1^K50R Gene Delivery in the Presence of IL-6

KAS cells were transfected with either control siRNA (hcon) or human eIF5A1 siRNA (h5A1) using Lipofectamine 2000. Seventy-two hours later the cells were re-transfected with siRNA. PEI complexes of empty vector (mcs) or eIF5A1^K50R (K50R) plasmids were added to the cells four hours later following removal of siRNA transfection medium. The growth medium used throughout the study contained IL-6. Apoptosis was measured seventy-two hours later by staining the cells with Annexin/PI and FACS analysis. See FIG. 7F.

Example 7

Co-Administration of eIF-5A1 Plasmid and eIF-5A1 siRNA Delays Growth of Multiple Myeloma Subcutaneous Tumors (FIGS. 8-10)

SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. Six 3-5 week old SCID/CB17 mice were injected with 10 million KAS-6/1 myeloma cells in 200 μL, PBS in their right flank and treatment was initiated when the tumors reached a minimum size of 4 mm³.

Control mice were injected intra-tumorally 2 times per week with PEI complexes containing pCpG-mcs (empty vector) and control siRNA (control group was made up of 3 mice: C-1, C-2, and C-3). Treated mice were injected intra-tumorally 2 times per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1k50R and eIF5A1 siRNA (treated group was made up of 3 mice: 5A-1, 5A-2, and 5A-3). Injections were given at multiple sites within the tumor to prevent reflux and a slow rate of injection was used to increase uptake. The data in FIG. 8 shows the tumor volume for all the mice in the group. The data shown in FIG. 9 is the average tumor volume per group+/−standard error. Asterix denote statistical significance (*=p<0.025; n=3).

FIG. 10 shows that co-administration of eIF-5A1 plasmid and eIF-5A1 siRNA reduces the weight of multiple myeloma subcutaneous tumors. The data shown is the average tumor weight per group+/−standard error. Asterix denote statistical significance (*=p<0.05; n=3).

JET-PEI (PolyPlus) at 2×0.1 ml was used for the in vivo tests. The N/P ratio was 8. The PEI/DNA/siRNA complexes were formed in a total volume of 0.1 ml in 5% glucose. The protocol for forming complexes was as follows.

• 1. Bring components to room temperature. Keep sterile.
• 2. Dilute 20 iLig of plasmid DNA (˜10 μl at 2 mg/ml) and 10 iLig siRNA (10 μl at 1 mg/ml) into a total volume of 25 μl. Use sterile water to make up difference.
• 3. Adjust the volume of DNA solution to 50μ 15% glucose by adding 25 μl of 10% glucose. Vortex gently and centrifuge briefly.
• 4. Dilute 4.8 μl of in vivo JETPEI into a total volume of 25 μl of 10% glucose. Adjust volume to 50 μl with sterile water to end up with a final concentration of 5% glucose. Vortex gently and centrifuge briefly.
• 5. Immediately add 50 μl of diluted PEI to the 50 μl of diluted DNA (do not reverse the order). Vortex briefly and immediately spin down.
• 6. Incubate for 15 minutes prior to injection. Complexes are stable for 6 hours.

CpG-free Cloning Vectors and pCpG Plasmids were obtained from InvivoGen. These plasmids are completely devoid of CpG dinucleotides, named pCpG. These plasmids yield high levels of transgene expression both in vitro and in vivo, and in contrast to CMV-based plasmids allow sustained expression in vivo. pCpG plasmids contain elements that either naturally lack CpG dinucleotides, were modified to remove all CpGs, or entirely synthesized such as genes encoding selectable markers or reporters. Synthesis of these new alleles was made possible by the fact that among the sixteen dinucleotides that form the genetic code, CG is the only dinucleotide that is non-essential and can be replaced. Eight codons contain a CG encoding for five different amino acids. All eight codons can be substituted by at least a choice of two codons that code for the same amino acid to create new alleles that code for proteins having amino acid sequences that remain identical to the wild type and thus are as active as their wild-type counterparts. These new alleles are available individually in a plasmid named pMOD from which they can be easily excised.

pCpG plasmids allow long lasting expression in vivo, and represent valuable tools to study the effects of CpGs on gene expression in vivo and in vitro, using cell lines expressing TLR9, as well as their effects on the innate and acquired immune systems.

The empty vector, pCpG-mcs (Invivogen) is a vector with no expressed gene product, only a multiple cloning site, and was used as the control vector. An HA-tagged eIF5A1^K50R cDNA was subcloned into the NcoI and NheI sites of a pCpG-LacZ vector (Invivogen), from which the LacZ gene had been removed, to give rise to the treatment vector pCpG-eIF5A1(K50R). The DNA was prepared using Endo-Free Qiagen kit. Endotoxin levels measured and are <0.03 EU/ug; DNA should be at 2 mg/ml in water.

The control siRNA used in the experiments was a micro-array validated non-targeting control siRNA from Dharmacon (D-001810-01). The siRNA was obtained with a modification (siSTABLE) to prevent degradation in serum.

The eIF5A1 siRNA used in the experiments was designed against the 3′UTR of human eIF5A1. There is no similarity between the eIF5A1 siRNA and mouse eIF5A1 and the siRNA should therefore only suppress human (but not mouse) eIF5A1. The siRNA also has no similarity to eIF5A2 (either human or mouse). The siRNA was obtained with a modification (siSTABLE) to prevent degradation in serum. The eIF5A1 siRNA has the following target sequence:

5′ GCU GGA CUC CUC CUA CAC A (UU) 3

The siSTABLE siRNA was dissolved at 1 mg/ml in water (stored in aliquots at −20C).

Tumor dimensions of length (l) and width (w) were measured 2-3 times per week using digital calipers. Tumor volume was calculated according to the following equation:

l=length; smallest dimension

w=width; largest dimension

tumor volume (mm³)=l²*w*0.5

Statistical Analyses

Student's t-test was used for statistical analysis. Significance was deemed to be a confidence level above 95% (p<0.05).

Example 8

Co-administration of eIF5A1 plasmid and eIF5A1 siRNA delays growth of multiple myeloma subcutaneous tumors and results in tumor shrinkage

In another study, again SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. Control mice were injected intra-tumorally 2 times per week with PEI complexes containing pCpG-mcs (empty vector) and control siRNA (control group G-1, G-2 and G-3). Treated mice were injected intra-tumorally 2 times per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1k50R (20 iLig of plasmid DNA) and eIF5A1 siRNA (10 iLig of siRNA) (treated group G-4, G-5 and G-6). The data shown in FIG. 11 is the average tumor volume per group+/−standard error. Asterix denote statistical significance (*=p<0.025; n=3). Six injections over a period of 21 days were given (red arrows).

Example 9

Administration of eIF5A1 siRNA Intra-Venously (i.v.) and PEI/eIF5A1K50R Plasmid Complexes Intra-Tumorally (i.t.) Results in Tumor Shrinkage of Multiple Myeloma Subcutaneous Tumors (Group 2B)

SCID mice were injected subcutaneously with KAS cells. When palpable tumors were observed treatment was initiated with an initial tail injection of 50 micrograms of either control siRNA (control group) or human eIF5A1 siRNA (treated group). Control Mice were subsequently treated by intra-tumoral injections 2 times per week with PEI complexes containing pCpG-mcs (empty vector; control group; G-1, G-2, and G-3). Treated mice were subsequently treated by intra-tumoral injections 2 times per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1k50R (20 μg plasmid DNA) (treated group; G-4, G-5, and G-6). Control mice continued to receive control siRNA (control group R-1, R-2, and R-3) by i.v. injection once per week. Treated mice continued to receive human eIF5A1 siRNA (20 μg) (treated group R-4, R-5, and R-6) by i.v. injection once per week. The data shown in FIG. 12 is the tumor volume for all the mice in each group. Six intramural injections of PEI/DNA (red arrows) and four i.v. injections of siRNA (blue arrows) were given over a period of 21 days.

FIG. 13 provides an overlay of the results from Example 8 and 9. SCID mice were injected subcutaneously with KAS cells. The data shown in FIG. 13 is the average tumor volume for the mice in each group+/−standard error. Asterix denote statistical significance between treated and control groups (**=p<0.01; ***=p<0.001; n=3).

Protocol for Forming PEI Complexes:

• 1. Bring components to room temperature. Keep sterile.
• 2. Dilute plasmid DNA or plasmid DNA+siRNA into a total volume of 25 μl. Use sterile water to adjust the volume.
  a) For plasmid DNA only complexes:
  Dilute 20 iLig of plasmid DNA (10 μl at 2 mg/ml) into a total volume of 25 μl. Use sterile water to make up difference.
• b) For plasmid DNA+siRNA complexes:
  Dilute 20 iug of plasmid DNA (˜10 μl at 2 mg/ml) and 10 iug of siRNA (10 μl at 1 mg/ml) into a total volume of 25 μl. Use sterile water to make up difference.
• 3. Adjust the volume of DNA solution to 50 μl 5% glucose by adding 25 μl of 10% glucose (provided with PEI kit). Vortex gently and centrifuge briefly.
• 4. Dilute in vivo JETPEI into a total volume of 25 μl of 10% glucose.
  a) For plasmid DNA only complexes:
  Dilute 3.2 μl of in vivo JETPEI into a total volume of 25 μl of 10% glucose. Adjust volume to 50 μl with sterile water to end up with a final concentration of 5% glucose. Vortex gently and centrifuge briefly.
  b) For plasmid DNA+siRNA complexes:
  Dilute 4.8 μl of in vivo JETPEI into a total volume of 25 μl of 10% glucose. Adjust volume to 50 μl with sterile water to end up with a final concentration of 5% glucose. Vortex gently and centrifuge briefly.
• 5. Immediately add 50 μl of diluted PEI to the 50 μl of diluted DNA (do not reverse the order!). Vortex briefly and immediately spin down.
• 6. Incubate for 15 minutes prior to injection. Complexes are stable for 6 hours.

Regarding the tail-vein injection of siRNA, the initial siRNA injection was 50 micrograms. siRNA was diluted to 0.4 mg/ml in PBS. 125 μl per mouse (50 iug) was injected into the tail vein. Subsequent injections of serum-stabilised siRNA were given two times per week at 20 iug per mouse. siRNA was diluted to 0.4 mg/ml in PBS. 50 μl per mouse (20 iug) was injected into the tail vein.

FIG. 13B shows that co-administration of eIF5A1 plasmid and eIF5A1 siRNA results in tumor shrinkage. SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. Mice were injected intra-tumorally 2 times per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1k50R and eIF5A1 siRNA (treated group; G-4, G-5, and G-6). Six injections over a period of 21 days were given. Forty-two days after the initiation of treatment the mice were sacrificed and the skin under the tumor site was opened and examined for evidence of tumor growth. No tumor growth was observed in any of the group 2A treated mice.

FIG. 13C shows that administration of eIF5A1 siRNA intra-venously (i.v.) and PEI/eIF5A1K50R plasmid complexes intra-tumorally (i.t.) results in tumor shrinkage of multiple myeloma subcutaneous tumors. SCID mice were injected subcutaneously with KAS cells. When palpable tumors were observed treatment was initiated with an initial injection of 50 micrograms of human eIF5A1 siRNA (treated group). Mice were subsequently treated by intra-tumoral injections 2 times per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1k50R (treated group; R-4, R-5, and R-6). Mice continued to receive human eIF5A1 siRNA by i.v. injection once per week. Treatment ended 21 days after initiation of treatment. Forty-two days after the initiation of treatment the mice were sacrificed and the skin under the tumor site was opened and examined for evidence of tumor growth. There was no evidence of tumor growth in one mouse of the treatment group (group 2B).

Example 10

Intra-Venous Co-Administration of eIF5A1 Plasmid and eIF5A1 siRNA Delays Growth of Multiple Myeloma Subcutaneous Tumors

SCID mice were injected subcutaneously with KAS cells. When palpable tumors were observed treatment was initiated with an initial injection of 50 micrograms of either control siRNA (control group) or human eIF5A1 siRNA (treated group). Mice were subsequently treated by intra-venous (red arrows) or intra-peritoneal injections (green arrow)—twice per week with either PEI complexes containing pCpG-mcs (empty vector; control group A1, A2, and A3) or PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1k50R (treated group; A4, A5, and A6). Mice continued to receive either control siRNA (control group A1, A2, and A3) or human eIF5A1 siRNA (treated group A4, A5, and A6) by i.v. injection (blue arrows) once per week. The data shown is the tumor volume for all the mice in each group. The data shown in FIG. 14 is the tumor volume for all the mice in each group.

Example 11

Administration of eIF5A1 siRNA Intra-Venously (i.v.) and PEI/eIF5A1K50R Plasmid Complexes Intra-Venously (i.v.) or Intra-Peritoneal (i.p.) Delays Growth of Multiple Myeloma Subcutaneous Tumors

SCID mice were injected subcutaneously with KAS cells. When palpable tumors were observed treatment was initiated with an initial injection of 50 micrograms of either control siRNA (control group) or human eIF5A1 siRNA (treated group). Control mice were subsequently treated by intra-venous or intra-peritoneal injections—once per week with PEI complexes containing pCpG-mcs (empty vector; control group was three mice: B1, B2,and B3). Treated mice were subsequently treated by intra-venous or intra-peritoneal injections—once per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1^K50R (treated group; B4, B5, and B6). Mice continued to receive either control siRNA (control group B1, B2, and B3) or human eIF5A1 siRNA (treated group was three mice: B4, B5, and B6) by i.v. injection once per week. The experiment began with initial siRNA injection of 50 μg (day-2 on graph in FIG. 15). Subsequent injections used 20 micrograms of siRNA once weekly. The siRNA was given naked, i.e. no delivery vehicle. PEI complexes contained 20 μg of plasmid DNA. The initial PEI injection was given i.p. and subsequent injections were given i.v. The data shown in FIG. 15 is the tumor volume for all the mice in each group.

FIG. 16 provides an overlay of Example 10 and 11. SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. One set of mice received i.v. injections of either control siRNA (control; Group A) or eIF5A1 siRNA (treated; Group A) once per week and either i.v. or i.p. of either PEI complexes containing pCpG-mcs (control; Group A) or PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1^K50R (treated; Group A). A second set of mice were given i.v. or i.p. injections ˜2 times per week with either PEI complexes containing pCpG-mcs (empty vector) and control siRNA (control; Group B.) or PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1k50R and eIF5A1 siRNA (treated; Group B). The data shown is the average tumor volume for the mice in each group+/standard error. Asterix denote statistical significance between treated and control groups (*=p<0.05; ***=p<0.001; n=3).

The protocols for preparing the PEI complexes and the siRNA are as described in previous examples.

Example 12

Co-Administration of eIF5A1 Plasmid and eIF5A1 siRNA Delays Growth of Multiple Myeloma Subcutaneous Tumors and Results in Tumor Shrinkage

SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. Control mice were injected intra-tumorally 2 times per week with PEI complexes containing pCpG-mcs (empty vector) and control siRNA (control group had 3 mice: control 1, control 2, and control 3). Treated mice were injected intra-tumorally 2 times per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1^K50R and eIF5A1 siRNA (treated group contained 4 mice: 5A-1, 5A-2, 5A-3, and 5A-4). The intra-tumoral rejections of PEI complexes contained both 20 iLig of plasmid DNA and 10 iLig of siRNA. The data shown in FIGS. 17A and 17B is the tumor volume for all the mice in each group.

Example 13

Administration of eIF5A1 siRNA Intra-Venously (i.v.) and PEI/eIF5A1^K50R Plasmid Complexes Intra-Tumorally (i.t.) Results in Tumor Shrinkage of Multiple Myeloma Subcutaneous Tumors

SCID mice were injected subcutaneously with KAS cells. When palpable tumors were observed treatment was initiated with an initial injection of 50 micrograms of either control siRNA (control group had three mice: control 1, control 2 and control 3) or human eIF5A1 siRNA (treated group had 3 mice: 5A-1, 5A-2, 5A-3). Control mice were subsequently treated by intra-tumoral injections 2 times per week with PEI complexes containing pCpG-mcs (20 μg) (control group 1-3). Treated mice were subsequently treated by intra-tumoral injections 2 times per week with PEI complexes containing the RNAi-resistant plasmid pCpG-eIF5A1^K50R (20 μg) (5A-1, 5A-2, 5A-3). Control mice continued to receive either control siRNA (20 μg) by tail vein i.v. injection twice per week. Treated mice continued to receive human eIF5A1 siRNA (20 μg) by tail vein i.v. injection twice per week. The injections were given 48 hours prior to the intra-tumoral injections. The siRNA was given as naked siRNA, i.e. no delivery vehicle. The data shown in FIGS. 18A and 18B is the tumor volume for all the mice in each group.

Example 14

Co-Administration of eIF5A1^K50R Plasmid, Driven by Either the EF1 or B29 Promoter, and eIF5A1 siRNA Delays Growth of Multiple Myeloma Subcutaneous Tumors and Results in Tumor Shrinkage

SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. Mice were injected intra-tumorally 2 times per week with PEI complexes containing either control vector (G1 and G2) or an eIF5A1 plasmid driven by either the B29 promoter (G3 and G4) or the EF1 promoter (G5 and G6) and either control siRNA (G1, G3, G5) or h5A1 siRNA (G2, G4, G6). The data shown is the average tumor volume+/−standard error for each group. Note: the B29 promoter was intended as a B-cell-specific promoter. However, although the B29 promoter/mCMV enhancer used in this study was found to drive high expression of HA-eIF5A1^K50R in KAS cells in vitro, it does not appear to be B-cell-specific (likely due to CMV enhancer). See FIG. 19.

Example 15

Co-Administration of eIF5A1 siRNA Increases Anti-Tumor Effect of eIF5A1^K50R Plasmid, Driven by Either the EF1 or B29 Promoter, on Multiple Myeloma Subcutaneous Tumors and Results in Reduced Tumor Burden

SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. Mice were injected intra-tumorally 2 times per week with PEI complexes containing either control vector (G1 and G2) or an eIF5A1 plasmid driven by either the B29 promoter (G3 and G4) or the EF1 promoter (G5 and G6) and either control siRNA (G1, G3, G5) or h5A1 siRNA (G2, G4, G6). The mice were sacrificed 24 days after the initiation of treatment and the subcutaneous tumor was removed and weighed. The data shown is the average tumor weight+/−standard error for all groups. See FIG. 20.

Example 16

eIF5A1 siRNA Synergistically Increases Apoptosis Induction Resulting from Infection with Ad-eIF5A in Lung Adenocarcinoma Cells

A549 cells were infected with either Ad-LacZ or Ad-eIF5A. Cells were transfected with either a control siRNA or an siRNA targeting human eIF5A1 (h5A1) by adding the transfection media to cells immediately following addition of the virus. Four hours after transfection with the siRNA and infection with virus, the media was replaced with fresh media and the cells were incubated for 72 hours prior to labelling with Annexin/PI to detect apoptotic cells. Note: over-expression of eIF5A in this cell line results in the accumulation of unhypusinated eIF5A due to limiting amounts of DHS and DOHH and therefore results in same pro-apoptotic effect as over-expression of eIF5A^K50R. These data indicate that the synergistic effect in apoptosis caused by simultaneous suppression of hypusinated eIF5A and over-expression of unhypusinated eIF5A is observed in non-myeloma tumor-types as well. See FIG. 21.

Example 17

Construction of Plasmid pExp5A

pExp5A is an expression plasmid with reduced CpG dinucleotides designed to drive expression of human eIF5A1^K50R predominantly in cells of B cell lineage. The vector is derived from pCpG-LacZ, a plasmid completely devoid of CpG dinucleotides (Invivogen). All the elements required for replication and selection in E. coli are free of CpG dinucleotides. The original CMV enhancer/promoter and LacZ gene from the CpG-LacZ vector have been replaced with a human minimal B cell specific promoter (B29/CD79b; Invivogen) and human eIF5A1^K50R, respectively, in order to drive B-cell specific expression of eIF5A1^K50R. The B29 DHS4.4 3′ enhancer has been introduced into the plasmid downstream of the eIF5A1 expression cassette in order to enhance activity of the B29 promoter and reduce expression in non-B cells (Malone et al. 2006. B29 gene silencing in pituitary cells is regulated by its 3′ enhancer. J. Mol. Biol. 362: 173-183). Incorporation of the B29 minimal promoter, eIF5A1^K50R, and the B29 DHS4.4 3′ enhancer has introduced 32 CpG dinucleotides into the vector.

Elements for Expression in E. coli
Origin of replication: E. coli R6K gamma ori.
* Due to the presence of the R6K gamma origin of replication, pCpG plasmids can only be amplified in E. coli mutant strain expressing a pir mutant gene. They will not replicate in standard E. coli strains. Therefore, pCpG plasmids are provided with the E. coli GT115 strain, a pir mutant also deficient in Dcm methylation (Invivogen). Bacterial promoter: EM2K, a CpG-free version of the bacterial EM7 promoter. Selectable marker: Zeocin™ resistance gene; a synthetic allele with no CpGs.

Elements for Expression in Mammalian Cells

Mammalian promoter: the human −167 bp minimal B29 (CD79b) promoter for tissue-specific expression in B cells. A synthetic intron (I 140) is also present in the 5′UTR. Polyadenylation signal: a CpG dinucleotide-free version of the late SV40 polyadenylation signal. 3′ Enhancer: the human B29 DHS4.4 3′ enhancer.
MAR: Two CpG-free Matrix attached regions (MAR) are present between the bacterial and mammalian transcription units. One MAR is derived from the 5′ region of the human IFN-I3 gene and one from the 5′ region of the β-globin gene.

The predicted Sequence of pExp5A (3371 bp is provided at FIG. 23.

Amino Acid Sequence of eIF5A1^K50R

* K50R mutation is underlined

MADDLDFETGDAGASATFPMQCSALRKNGFVVLKGRPCKIVEMSTSKTG
RHGHAKVHLVGIDIFTGKKYEDICPSTHNMDVPNIKRNDFQLIGIQDGY
LSLLQDSGEVREDLRLPEGDLGKEIEQKYDCGEEILITVLSAMTEEAAV
AIKAMAK

Construction of pExp5A—Outline of Construction:
Step 1: Cloning of B29 DHS4.4 3′ enhancer and subcloning into pGEM T easy (Promega)—creates pGEM-4.4enh #8.
Step 2: Subcloning of minimal B29 promoter into pCpG-LacZ (Invivogen)—creates B29-5 #3.
Step 3: Subcloning of HA-eIF5A1^K50R into B29-5#3 vector—creates B29-5#3-e1F5A1^K50R.
Step 4: Creation of new multiple cloning site in pCpG-mcs (Invivogen)—creates pCpG-Linker4.
Step 5: Subcloning of B29 DS4.4 3′ enhancer into pCpG-Linker4—creates pCpG-DHS4.4.
Step 6: Subcloning of B29 promoter+HA-eIF5A1^K50R+SV40 pA expression cassette into pCpG-DHS4.4 creates pExp-5.
Step 7: Replacement of HA-eIF5A1^K50R in pExp-5 with non-HA eIF5A1^K50R creates final vector, pExp5A.

Construction in Detail:

Step 1: Cloning of B29 DHS4.4 3′ Enhancer and Subcloning into pGEM T Easy (Promega)—Creates pGEM-4.4Enh #8.

The B29 DHS4.4 3′ enhancer was cloned by PCR from genomic DNA isolated from KAS cells (human multiple myeloma cell line) using the following primers: forward 5′-CAGCAAGGGAGCACCTATG-3′ and reverse 5′-GTTGCAGTGAGCGGAGATG-3′. The primers were designed using the sequence of the human CD79B/GH-1 Intergenic region (Accession AB062674). The resulting 608 bp PCR fragment was subcloned into the pGEM® T easy cloning vector (Promega) and sequenced. Komatsu et al. 2002. Novel regulatory regions found downstream of the rat B29/Ig-b gene. Eur. J. Biochem. 269: 1227-1236.

Sequence of B29 DHS4.4 3′ Enhancer PCR Fragment (297 Bp) in pGEM-4.4Enh #8

ACCACCCTGGGCCAGGCTGGGCCAAGCCAGGCGGCCCCTGTGTTTTCCC
CAGTCTCTGGGCTGCTGGAGGGAACCAGGTTGTTTTGGCATCAGCCTCT
ACTGAGCCGGAGCCCTTCCTTTCCTGCTGCTTTGCATAGTGGCACTAAT
TCCGTCCTCCTACCTCCACCAGGGACCTAGGCAGCCGGGTAGATGGTGG
GAGGAGGCTTCACTTCTCCCCCAAGCAGGGTCTCCACCTGCTTGAGGCT
GCCCTGGGTTGGGGGAGGCCTTGGCTTTACCTAAAGACTTTTTAACACC
TCT

• • +4.4 regions contains several transcription factor binding sites

SRY GTTGTTT
GATA CATCAGC
OCT-X GCTGCTTTGCATAG
NF-KB GAGGCTGCCC

Alignment of B29 DHS4.4 3′ Enhancer PCR Fragment (297 Bp) in pGEM-4.4Enh #8 with Sequence of the Human CD79B/GH-1 Intergenic Region (Accession AB062674).

Step 2: Subcloning of Minimal B29 Promoter into pCpG-LacZ (Invivogen)—Creates B29-5 #3.

The minimal −167 human B29 promoter was amplified from a commercial plasmid bearing the full length human B29 promoter (pDrive-hB29; Invivogen) using the following primers: forward 5′-CCAACTAGTGCGACCGCCAAACCTTAGC-3′; reverse: 5′-CAAAAGCTTGACAACGTCCGAGGCTCCTTGG-3′. The resulting PCR fragment was digested with SpeI and HindIII and ligated into the SpeI and HindIII sites of the pCpG-LacZ vector (Invivogen) to create B29-5 #3.

Sequence of B29 Minimal Promoter PCR Fragment (188 Bp) in B29-5 #3

GCGACCGCCAAACCTTAGCGGCCCAGCTGACAAAAGCCTGCCCTCCCCC
AGGGTCCCCGGAGAGCTGGTGCCTCCCCTGGGTCCCAATTTGCATGGCA
GGAAGGGGCCTGGTGAGGAAGAGGCGGGGAGGGGACAGGCTGCAGCCGG
TGCAGTTACACGTTTTCCTCCAAGGAGCCTCGGACGTTGTC

Alignment of B29 Minimal Promoter PCR Fragment (B29 Min) in B29-5 #3 with Full Length Human B29 Promoter from pDrive-hB29

Step 3: Subcloning of HA-eIF5A11(50R into B29-5#3 Vector—Creates pB29-eIF5A1K50R_—7.

HA-eIF5A1^K50R was amplified by PCR using the pHM6-eIF5A1^K50R as a DNA template and the following primers: forward 5′-CGCCATGGACATGTACCCTTACGACGTCCCAGACTACGCTGCAGATGATTTG GACTTCGAG-3′ and reverse 5′-CGCGCTAGCCAGTTATTTTGCCATCGCC-3′. The resulting PCR fragment was digested with NcoI and NheI and subcloned into the NcoI and NheI sites of B29-5 #3 to replace LacZ.

Sequence of HA-eIF5A1K50R PCR Fragment (497 Bp) in pB29-eIF5A1K50R 7

ACATGTACCCTTACGACGTCCCAGACTACGCTGCAGATGATTTGGACTT
CGAGACAGGAGATGCAGGGGCCTCAGCCACCTTCCCAATGCAGTGCTCA
GCATTACGTAAGAATGGTTTTGTGGTGCTCAAGGGCCGGCCATGTAAGA
TCGTCGAGATGTCTACTTCGAAGACTGGCAGGCATGGCCATGCCAAGGT
CCATCTGGTTGGCATTGATATTTTTACTGGGAAGAAATATGAAGATATC
TGCCCGTCGACTCATAACATGGATGTCCCCAACATCAAAAGGAATGATT
TCCAGCTGATTGGCATCCAGGATGGGTACCTATCCCTGCTCCAGGACAG
TGGGGAGGTACGAGAGGACCTTCGTCTGCCTGAGGGAGACCTTGGCAAG
GAGATTGAGCAGAAGTATGACTGTGGAGAAGAGATCCTGATCACAGTGC
TGTCCGCCATGACAGAGGAGGCAGCTGTTGCAATCAAGGCGATGGCAAA
ATAACTG

Translation of HA-eIF5A1^K50R PCR fragment in pB29-eIF5A1K50R 7

HA Epitope

eIF5A1^K50R

K50R

MDMYPYDVPDYAADDLDFETGDAGASATFPMQCSALRKNGFVVLKGRPC
KIVEMSTSKTGRHGHAKVHLVGIDIFTGKKYEDICPSTHNMDVPNIKRN
DFQLIGIQDGYLSLLQDSGEVREDLRLPEGDLGKEIEQKYDCGEEILIT
VLSAMTEEAAVAIKAM AK

Alignment of HA-eIF5A1^K50R PCR Fragment in pB29-eIF5A1K50R 7 with Human eIF5A1 (Accession # NP 001961)

Step 4: Creation of New Multiple Cloning Site in pCpG-Mcs (Invivogen)—Creates pCpG-Linker4.

The pCpG cloning vector, pCpG-mcs G2 (Invivogen), was digested with EcoRI to remove the mammalian expression cassette containing the mCMV enhancer, the hEF1 promoter, the synthetic intron, the multiple cloning site, and the SV40 polyadenylation signal. The EcoRI-digested pCpG-mcs G2 vector was then ligated to a synthetic linker with EcoRI sticky ends to create a promoterless vector with a new multiple cloning site (pCpG-Linker4).

Synthetic Linker, Linker4 with Two Eco RI Sticky Ends

Sequence of Region Surrounding New Multiple Cloning Site in pCpG-Linker4

1 GGCATGTGAACTGGCTGTCTTGGTTTTCATCTGTACTTCATCTGCTACCT   50
51 CTGTGACCTGAAACATATTTATAATTCCATTAAGCTGTGCATATGATAGA  100
101 TTTATCATATGTATTTTCCTTAAAGGATTTTTGTAAGAACTAATTGAATT  150
151 GATACCTGTAAAGTCTTTATCACACTACCCAATAAATAATAAATCTCTTT  200
201 GTTCAGCTCTCTGTTTCTATAAATATGTACAAGTTTTATTGTTTTTAGTG  250
251 GTAGTGATTTTATTCTCTTTCTATATATATACACACACATGTGTGCATTC  300
301 ATAAATATATACAATTTTTATGAATAAAAAATTATTAGCAATCAATATTG  350
351 AAAACCACTGATTTTTGTTTATGTGAGCAAACAGCAGATTAAAAGGAATT  400
401 CTCGAGTCATCGATAAGCGGCCGCAGACGCGTAATTCAGTCAATATGTTC  450
451 ACCCCAAAAAAGCTGTTTGTTAACTTGCCAACCTCATTCTAAAATGTATA  500
501 TAGAAGCCCAAAAGACAATAACAAAAATATTCTTGTAGAACAAAATGGGA  550
551 AAGAATGTTCCACTAAATATCAAGATTTAGAGCAAAGCATGAGATGTGTG  600
601 GGGATAGACAGTGAGGCTGATAAAATAGAGTAGAGCTCAGAAACAGACCC  650
651 ATTGATATATGTAAGTGACCTATGAAAAAAATATGGCATTTTACAATGGG  700
701 AAAATGATGATCTTTTTCTTTTTTAGAAAAACAGGGAAATATATTTATAT  750
751 GTAAAAAATAAAAGGGAACCCATATGTCATACCATACACACAAAAAAAAT  800
801 TCCAGTGAATTATAAGTCTAAATGGAGAAGGCAAAACTTTAAATCTTTTA  850
851 GAAAATAATATAGAAGCATGCCATCAAGACTTCAGTGTAGAGAAAAATTT  900
901 CTTATGACTCAAAGTCCTAACCACAAAGAAAAGATTGTTAATTAGATTGC  950
951 ATGAATATTAAGACTTATTTTTAAAATTAAAAAACCATTAAGAAAAGTCA 1000
1001 GGCCATAGAATGACAGAAAATATTTGCAAC                     1030

The numbering of the sequence above is for ease of reference to the following features: 13Glo MAR (nucleotides 1-380); EcoRI recognition sequence (nucleotides 396-401); XhoI recognition sequence (nucleotides 401-406); ClaI recognition sequence (nucleotides 409-414); NotI recognition sequence (nucleotides 417-424); MluI recognition sequence (nucleotides 427-432);IFNB S/MAR (nucleotides 438-1,030).
Step 5: Subcloning of B29 DS4.4 3′ Enhancer into pCpG-Linker4—Creates pCpG-DHS4.4.

The B29 DHS4.4 3′ enhancer was amplified by PCR using pGEM-4.4enh #8 as a template and the following primers: forward 5′-GAAGCGGCCGCACCACCCTGGGCCAGGCTGG-3′; and reverse 5′-CCACGCGTAGAGGTGTTAAAAAGTCTTTAGGTAAAG-3′. The resulting PCR fragment was digested with NotI and MluI and ligated into the NotI and MluI sites in the new multiple cloning site of pCpG-Linker4 to create pCpG-DHS4.4.

>pCpG-DHS4.4 Full-Length Sequences (2,282 bp)

1 TTAATTAAAATTATCTCTAAGGCATGTGAACTGGCTGTCTTGGTTTTCAT   50
51 CTGTACTTCATCTGCTACCTCTGTGACCTGAAACATATTTATAATTCCAT  100
101 TAAGCTGTGCATATGATAGATTTATCATATGTATTTTCCTTAAAGGATTT  150
151 TTGTAAGAACTAATTGAATTGATACCTGTAAAGTCTTTATCACACTACCC  200
201 AATAAATAATAAATCTCTTTGTTCAGCTCTCTGTTTCTATAAATATGTAC  250
251 AAGTTTTATTGTTTTTAGTGGTAGTGATTTTATTCTCTTTCTATATATAT  300
301 ACACACACATGTGTGCATTCATAAATATATACAATTTTTATGAATAAAAA  350
351 ATTATTAGCAATCAATATTGAAAACCACTGATTTTTGTTTATGTGAGCAA  400
401 ACAGCAGATTAAAAGGAATTCTCGAGTCATCGATAAGCGGCCGCACCACC  450
451 CTGGGCCAGGCTGGGCCAAGCCAGGCGGCCCCTGTGTTTTCCCCAGTCTC  500
501 TGGGCTGCTGGAGGGAACCAGGTTGTTTTGGCATCAGCCTCTACTGAGCC  550
551 GGAGCCCTTCCTTTCCTGCTGCTTTGCATAGTGGCACTAATTCCGTCCTC  600
601 CTACCTCCACCAGGGACCTAGGCAGCCGGGTAGATGGTGGGAGGAGGCTT  650
651 CACTTCTCCCCCAAGCAGGGTCTCCACCTGCTTGAGGCTGCCCTGGGTTG  700
701 GGGGAGGCCTTGGCTTTACCTAAAGACTTTTTAACACCTCTACGCGTAAT  750
751 TCAGTCAATATGTTCACCCCAAAAAAGCTGTTTGTTAACTTGCCAACCTC  800
801 ATTCTAAAATGTATATAGAAGCCCAAAAGACAATAACAAAAATATTCTTG  850
851 TAGAACAAAATGGGAAAGAATGTTCCACTAAATATCAAGATTTAGAGCAA  900
901 AGCATGAGATGTGTGGGGATAGACAGTGAGGCTGATAAAATAGAGTAGAG  950
951 CTCAGAAACAGACCCATTGATATATGTAAGTGACCTATGAAAAAAATATG 1000
1001 GCATTTTACAATGGGAAAATGATGATCTTTTTCTTTTTTAGAAAAACAGG 1050
1051 GAAATATATTTATATGTAAAAAATAAAAGGGAACCCATATGTCATACCAT 1100
1101 ACACACAAAAAAATTCCAGTGAATTATAAGTCTAAATGGAGAAGGCAAAA 1150
1151 CTTTAAATCTTTTAGAAAATAATATAGAAGCATGCCATCAAGACTTCAGT 1200
1201 GTAGAGAAAAATTTCTTATGACTCAAAGTCCTAACCACAAAGAAAAGATT 1250
1251 GTTAATTAGATTGCATGAATATTAAGACTTATTTTTAAAATTAAAAAACC 1300
1301 ATTAAGAAAAGTCAGGCCATAGAATGACAGAAAATATTTGCAACACCCCA 1350
1351 GTAAAGAGAATTGTAATATGCAGATTATAAAAAGAAGTCTTACAAATCAG 1400
1401 TAAAAAATAAAACTAGACAAAAATTTGAACAGATGAAAGAGAAACTCTAA 1450
1451 ATAATCATTACACATGAGAAACTCAATCTCAGAAATCAGAGAACTATCAT 1500
1501 TGCATATACACTAAATTAGAGAAATATTAAAAGGCTAAGTAACATCTGTG 1550
1551 GCTTAATTAAAACAGGTAGTTGACAATTAAACATTGGCATAGTATATCTG 1600
1601 CATAGTATAATACAACTCACTATAGGAGGGCCATCATGGCCAAGTTGACC 1650
1651 AGTGCTGTCCCAGTGCTCACAGCCAGGGATGTGGCTGGAGCTGTTGAGTT 1700
1701 CTGGACTGACAGGTTGGGGTTCTCCAGAGATTTTGTGGAGGATGACTTTG 1750
1751 CAGGTGTGGTCAGAGATGATGTCACCCTGTTCATCTCAGCAGTCCAGGAC 1800
1801 CAGGTGGTGCCTGACAACACCCTGGCTTGGGTGTGGGTGAGAGGACTGGA 1850
1851 TGAGCTGTATGCTGAGTGGAGTGAGGTGGTCTCCACCAACTTCAGGGATG 1900
1901 CCAGTGGCCCTGCCATGACAGAGATTGGAGAGCAGCCCTGGGGGAGAGAG 1950
1951 TTTGCCCTGAGAGACCCAGCAGGCAACTGTGTGCACTTTGTGGCAGAGGA 2000
2001 GCAGGACTGAGGATAACCTAGGAAACCTTAAAACCTTTAAAAGCCTTATA 2050
2051 TATTCTTTTTTTTCTTATAAAACTTAAAACCTTAGAGGCTATTTAAGTTG 2100
2101 CTGATTTATATTAATTTTATTGTTCAAACATGAGAGCTTAGTACATGAAA 2150
2151 CATGAGAGCTTAGTACATTAGCCATGAGAGCTTAGTACATTAGCCATGAG 2200
2201 GGTTTAGTTCATTAAACATGAGAGCTTAGTACATTAAACATGAGAGCTTA 2250
2251 GTACATACTATCAACAGGTTGAACTGCTGATC                   2282

The numbering of the sequence above is for ease of reference to the following features: 13Glo MAR (nucleotides 1-400); EcoRI recognition sequence (nucleotides 416-421); XhoI recognition sequence (nucleotides 421-426); ClaI recognition sequence (nucleotides 429-434); NotI recognition sequence (nucleotides 437-444); DHS4.4 (nucleotides 445-741); MluI recognition sequence (nucleotides 742-747);IFNB S/MAR (nucleotides 753-1,569).
Step 6: Subcloning of B29 Promoter+HA-eIF5A1K5° R+SV40 pA Expression Cassette into pCpG-DHS4.4—Creates pExp-5.

The B29-eIF5A1 expression cassette containing the minimal B29 promoter, the synthetic intron, HA-eIF5A1^K50R, and the SV40 pA, was amplified from pB29-eIF5A1K50R 7 (Step 3) by PCR using the following primers: forward 5′-GTTATCGATACTAGTGCGACCGCCAAACC-3′; and reverse 5′-CAAGCGGCCGCCATACCACATTTGTAGAGGTTTTAC-3′. The resulting PCR fragment was digested with ClaI and NotI and subcloned into the ClaI and NotI sites in the multiple cloning site of pCpG-DHS4.4 to create pExp-5.

Step 7: Replacement of HA-eIF5A1^K50R in pExp-5 with Non-HA eIF5A1^K50R Creates Final Vector, pExp5A.

The pExp-5 plasmid was digested with NcoI and NheI to remove HA-eIF5A1^K50R. A non-HA-tagged eIF5A1^K50R PCR fragment was amplified from pHM6-eIF5A1^K50R by PCR using the following primers: forward 5′-CACCATGGCAGATGATTTGGACTTC-3′; and reverse 5′-CGCGCTAGCCAGTTATTTTGCCATCGCC-3′. The resulting PCR product was digested with NcoI and NheI and ligated into the NcoI and NheI sites of B29-5 #3 to generate B29-K50R. B29-K50R was digested with NcoI and NheI and the 470 bp eIF5A1^K50R fragment was gel purified and ligated to NcoI/NheI-digested pExp-5 to generate the final expression vector, pExp5A.

Example 18

Testing of pExp5A

Various cell lines were transfected with plasmids using Lipofectamine 2000 and expression of HA-eIF5A1K50R was determined 24 hours following transfection by Western blotting with an anti-HA antibody (Roche). Different cells lines tested were P3X63Ag8.653 (mouse B lymphoblast—myeloma), KAS (human myeloma), HepG2 (human liver hepatocellular carcinoma), T24 (human bladder carcinoma); HT-29 (human colorectal adenocarcinoma), HEK-293 (human embryonic kidney cells), PC3 (human prostrate adenocarcinoma); HeLa (human cervical adenocarcinoma), and A549 (lung carcinoma). See FIGS. 24A and 24B.

pExp-5 plasmid expresses HA-eIF5A1^K50R in both human and mouse myeloma cell lines at comparable levels to a plasmid with the constitutive EF1 promoter (CpG-eIF5A1^K50R). However expression of HA-eIF5A1^K50R driven by pExp-5 is limited in non-B cell lines compared to expression by a constitutive promoter. The one exception was in HEK-293 cells, a human embryonic kidney cell line where high levels of HA-eIF5A1^K50R expression was observed following pExp-5 transfection—this may be due to the embryonic nature of the cell line; at this time we do not know if pExp-5 expresses in adult kidney cells. The final plasmid for use in toxicity studies and clinical trial will be a version of pExp-5 in which HA-eIF5A1K5° R has been replaced by non-HA tagged eIF5A1^K50R (pExp5A). pExp-5 contains HA-tagged eIF5A1^K50R under the control of the minimal human B29 promoter/enhancer; expression of HA-eIF5A1^K50R was compared to that driven by plasmids with constitutive expression as well as to a plasmid containing the full-length B29 promoter

Example 19

Formation of In Vivo JETPEI™ Nanoparticle

This example given is for formation of the in vivo JETPEI™ nanoparticle complex for injection into 20 g mouse for a dose of 1.5 mg/kg (0.1 mL)—1.5 mg/kg=1.0 mg pExp5A/kg+0.5 mg h5A1/kg—DNA:siRNA ratio=2:1.

Dilute plasmid DNA and siRNA into a total volume of 25 ml. Use sterile water to adjust the volume. * Dilute 20 mg of plasmid DNA (10 ml at 2 mg/ml) and 10 mg of siRNA (10 ml at 1 mg/ml) into a total volume of 25 ml. Use sterile water to make up difference. Adjust the volume of DNA solution to 50 ml 5% glucose by adding 25 ml of 10% glucose (provided with PEI kit). Vortex gently and centrifuge briefly. Dilute in vivo JETPEI™ into a total volume of 25 ml of water. * Dilute 3.6 ml of in vivo JETPEI™ into a total volume of 25 ml of water. Adjust final volume to 50 ml with 10% glucose to end up with a final concentration of 5% glucose. Vortex gently and centrifuge briefly. Immediately add 50 ml of diluted PEI to the 50 ml of diluted DNA (do not reverse the order!). Vortex briefly and immediately spin down.

After formation the complex is stable for 8 to 10 hours. The N/P ratio of the complex should be 6. The N/P ratio is the ratio of the number of positively charged nitrogen residues of in vivo-jetPEI to the number of negatively charged phosphate residues of DNA and siRNA. DNA and siRNA contain the same number of phosphate groups per gram. The N/P ratio is therefore a measure of the ionic balance within the complex. Increasing the N/P ratio of the complex can increase the toxicity of the complex. In vivo JET-PEI is provided as a 150 mM solution (expressed as nitrogen residues) while DNA contains 3 nmoles of anionic phosphate in 1 mg. The final concentration of DNA in the final volume should not exceed 0.5 mg/ml. The DNA should be of high quality and prepared in water. In vivo-jetPEI and 10% glucose should be brought to room temperature prior to use.

Example 20

Dose Range-Finding and Repeat Dose Studies with Intra-Venous SNS01 and SNS-EF1/UU in Mice

SNS01 is one embodiment of the present invention—it is a cancer therapy biologic targeted to the treatment of multiple myeloma. SNS01 is comprised of three components: a DNA vector expressing a pro-apoptotic mutant of eIF5A (see FIG. 22); an siRNA that targets the native eIF5A that promotes growth/anti-apoptosis of cancer cells (see the sequence in FIG. 25); and a synthetic polymer called polyethylenimine (In vivo-jetPEI; Polyplus Transfection Inc.) that acts as a delivery vehicle.

The purpose of the studies was to determine the maximum tolerated dose and the feasibility of long-term administration of therapeutic doses of intra-venous SNS01 into mice. Two separate studies were performed. The maximum tolerated dose (Study ID: MTD) study was an 8-day study in which mice received two intra-venous doses of increasing amounts of SNS01 (from 2.2 mg/kg to 3.7 mg/kg) and toxicity was assessed by monitoring clinical signs, body weight, organ weight and liver enzymes. The 9-week repeated dose study (Study ID: EX6) was a study designed to assess toxicity following long-term administration of twice-weekly therapeutic doses (1.5 mg/kg) of SNS-EF1/UU and as well as it's various components. SNS-EF1/UU is a preclinical version of SNS01 and differs mainly in that expression of eIF5A^K50R is driven by a constitutive promoter (one that expresses in all tissues at all times) rather than a B-cell-specific promoter as in the SNS01 complex. The use of the B cell-specific B29 promoter in SNS01 was designed to enhance the safety of the therapeutic by limiting expression of the pro-apoptotic eIF5A mutant to cells of B-cell origin, including myeloma cells. The EX6 study also included a group of mice that were dosed with a mouse-specific eIF5A siRNA to determine whether there were any toxic effects of suppressing eIF5A in mouse tissues. Toxicity in the repeated dose study was assessed by monitoring clinical signs, body weight, hematology, liver enzymes, as well as histopathology.

		Injection	Duration of
Study ID	Animal Model	Schedule	Treatment	Test Article
MTD	CD-1 (female)	Twice weekly	8-Days	SNS01
		Intra-venous	(2 injections)
EX6	Balb/c (female)	Twice weekly	9-Weeks	SNS-EF1/
		Intra-venous		UU
				SNS-EF1/
				UU
				components
				tested
				individually
				Mouse
				eIF5A
				siRNA

	Plasmid			Material
Test Article	DNA	siRNA	Vehicle	Grade
SNS01a	pExp5Ac	eIF5A	In vivo-	GLP-grade
	eIF5AK50R	siRNA	jetPEI ™	materials
	expression	(dTdT
	driven	overhangd)
	by B29	human-
	B-cell-	specific
	specific	eIF5A
	promoter)	siRNA
SNS-EF1/UUb	pCpG-HA-	h5Al	In vivo-	Research-grade
	eIF5AK50R	(UU	jetPEI ™	materials
	(HA-	overhangd)
	eIF5AK50R	human-
	expression	specific
	driven by	eIF5A
	ubiquitous	siRNA
	EF1
	promoter)
aSNS01 contains GLP-grade materials and is being developed for the clinic
bSNS-EF1/UU is a test article used in preclinical research that led to the development of SNS01
cthe pExp5A plasmid is RNAi-resistant due to the fact that the plasmid contains only the open reading frame of eIF5A while the eIF5A siRNA (h5A1) targets the 3′ UTR of eIF5A
dthe sequence of the SNS01 eIF5A siRNA and the h5A1 siRNA are identical except for the presencee of a dTdT overhang rather than a UU overhang on the 3′ terminal ends of the siRNA; the dTdT overhang does not affect the target selectivity or efficacy of the siRNA but has been proposed to enhance stability

Preclinical experiments have indicated that SNS01 is therapeutic at doses of 0.75 mg/kg to 1.5 mg/kg (Study EX9). In the 8-day dose range-finding study (Study ID: MTD) significantly higher doses than the therapeutic range was tested to determine the upper limit of the dose range. Twice-weekly intra-venous doses of the test article was well tolerated at the lower dose levels of 2.2 mg/kg and 2.9 mg/kg although one mouse reached morbidity at the 2.9 mg/kg and was euthanized. Doses at 3.3 mg/kg or above resulted in survival rates of approximately 20-25%. Therefore, the maximum tolerated dose is between 2.2 mg/kg and 2.9 mg/kg and is well above the therapeutic range of 0.75 mg/kg to 1.5 mg/kg.

In the 9-week repeated dose study (Study ID: EX6) the mice received twice weekly tail vein injections of therapeutic doses (1.5 mg/kg) of SNS-EF1/UU and no test article-related toxic effects were observed over the period of the study. The DNA and siRNA were also tested separately in this study and both were well tolerated by the mice. Since the human eIF5A siRNA is not active in mice, a mouse eIF5A-specific siRNA was also included in this study. No toxic effects related to chronic administration of the mouse eIF5A siRNA were observed over the 9-week period. These results indicate that therapeutic doses of SNS01 and SNS-EF1/UU are non-toxic to mice even when administered over long periods.

Test Article and Vehicle

	Manufacturer
	of Plasmid	Manufacturer of	Manufacturer
	DNA	siRNA	of PEI	Formation of
Test Article	component	component	component	Test Article
SNS01	VGXI	Avecia	Polyplus	Components
	Lot #		Transfection Inc	were combined
	pExp5A.08L007		GLP-Grade	with 10%
				glucose to form
				nano -
				complexes;
				complexes
				were injected
				within 2-4
				hours
SNS-EF1/UU	Qiagen	ThermoScientific	Polyplus	Components
	EndoFree	Dharmacon	Transfection	were combined
	Plasmid Mega	RNAi	Inc.	with 10%
	Kit	Technologies	Research-Grade	glucose to form
	<0.1 EU/μg			nano -
	DNA			complexes;
				complexes
				were injected
				within 2-4
				hours
Storage	−20° C.	−20°	4°	Room
Conditions	(≧1 year)	(≧1 year)	(≧1 year)	Temperature
(Stability)				(≧6 hours)

Test Systems and Study Designs

All aspects of this study were conducted in accordance with the guidelines set out by the University of Waterloo Animal Care Committee (Waterloo, Ontario, Canada) as established by the Canadian Council on Animal Care and the Province of Ontario Animals for Research Act. The CD-1 and BALB/c mice were obtained from Charles River Laboratories (Quebec, Canada). Mice from both studies received the test article twice-weekly via tail vein intravenous injections. Slow injections (˜2-3 minutes) were used to deliver volumes greater than 0.2 ml. The mice for the 8-day study were approximately 6-9 weeks old at the start of study. The mice for the 9-week repeated dose study were approximately 5-6 weeks old at the initiation of the study.

STUDY ID: MTD
	No.			Dose
	Animals		N/P	level	Injection	Total #
Group	(female)	Test Article	ratioa	(mg/kg)	Volume	injections
MTD-C	5	5%	—	—	0.33 mL	2
		Glucose
MTD-PA	5	SNS01	6	2.2	0.20 mL	2
				mg/kg
MTD-PB	5	SNS01	6	2.9	0.27 mL	2
				mg/kg
MTD-PC	4	SNS01	6	3.3	0.30 mL	lb
				mg/kg
MTD-PD	5	SNS01	6	3.7	0.33 mL	lb
				mg/kg
aN/P ratio = ratio of positively-charged nitrogens on PEI to the negatively-charged phosphate groups of the nucleic acids
b—due to toxicity the surviving mice were not given a second injection

STUDY ID: EX6
	No.
	Animals		N/P	Dose level	Injection	Total #
Group	(female)	Test Article	ratio	(mg/kg)	Volume	injections
Ex6-G1	4	5%	—	—	0.10 mL	20
		Glucose
Ex6-G2	5	Vehicle	8	1.5 mg/kg	0.10 mL	20
		Controla
Ex6-G3	5	siRNAb	8	1.5 mg/kg	0.10 mL	20
Ex6-G4	6	DNAc	8	1.5 mg/kg	0.10 mL	20
Ex6-G5	4	SNS-	8	1.5 mg/kg	0.10 mL	20
		EF1/UU
Ex6-G6	6	Mouse	8	1.5 mg/kg	0.10 mL	20
		siRNAd
aPEI complex containing a non-expressing plasmid (same vector background as pExp5A) and a non-targeting siRNA
bPEI complex containing a non-expressing plasmid (same vector background as pExp5A) and the h5Al siRNA
cPEI complex containing pCpG-HA-eIF5AK50R plasmid and a non-targeting siRNA
dPEI complex containing a non-expressing plasmid (same vector background as pExp5A) and a mouse-specific eIF5A siRNA (the human eIF5A siRNA is not active in mouse)

8-Day Maximum Tolerated Dose Study (MTD)

The two-dose 8-day study was a dose range-finding study designed to determine the maximum tolerated dose of SNS01. The dose range was 2.2 mg/kg to 3.7 mg/kg and is well above the therapeutic dose range of 0.75 mg/kg to 1.5 mg/kg. At the lowest dose (2.2 mg/kg) of SNS01 no clinical signs of toxicity were observed except for one mouse that exhibited slightly ruffled fur and decreased activity that resolved within one hour. No clinical signs of toxicity were observed following the 2^nd injection of 2.2 mg/kg of SNS01. All the mice maintained their weight throughout the study. No macroscopic changes in the organs were observed. The organ weight to body weight ratios were unchanged from the control group except for a modest increase in the ratio of the liver weight:body weight ratio. However, since an increase in this ratio was not observed in any of the higher dose level groups it is unlikely to be related to the test article.

Four out of five mice tolerated 2.9 mg/kg of SNS01 with no clinical signs of toxicity. However, one mouse experienced convulsions and mild respiratory distress within 1 hour of injection and had to be humanely euthanized. No clinical signs of toxicity were observed following the 2^nd injection of SNS01 in the remaining mice. The mice maintained their weight throughout the study and no macroscopic changes in the organs or changes in the organ weight to body weight ratios were observed. There was a slight increase in the serum levels of ALT following two doses of 2.9 mg/kg SNS01.

As expected, doses of SNS01 at or above 3.3 mg/kg were not well tolerated and in both groups all mice but one had to be humanely euthanized. In all cases where mice were humanely euthanized due to morbidity the clinical signs appeared within 1 hour of injection and were consistent with other reported studies using high doses of PEI. The surviving mice of the 3.3 mg/kg and 3.7 mg/kg recovered completely within 4 hours after the injection and maintained their weight throughout the study, although they did not receive a 2^nd dose. The maximum tolerated dose of SNS01 therefore appears to be between 2.2 mg/kg and 2.9 mg/kg.

9-Week Repeated Dose Study (EX6)

The purpose of the 9-week repeated dose study was to assess the safety of chronic administration of therapeutic doses (1.5 mg/kg) of SNS-EF1/UU, a complex that was used for preclinical studies during development of SNS01. SNS-EF1/UU does not differ significantly from SNS01, the major difference being that the materials are research-grade and that eIF5A^K50R expression is driven by the constitutive human EF1 promoter that is active in all cell types. Although SNS01 uses a B-cell-specific promoter to drive eIF5A^K50R expression, the use of a constitutive promoter in this safety study allows for the assessment of toxicity resulting from the accumulation of the mutant eIF5A^K50R protein in non-B-cell tissues. Another aspect of the 9-week repeated dose study was the inclusion of groups to test the safety of the individual components of SNS-EF1/UU. The DNA group (Ex6-G3) was dosed with a complex containing the eIF5A plasmid and a non-targeting control siRNA while the siRNA group (Ex6-G4) was dosed with a complex containing the human eIF5A (h5A1) siRNA and a non-expressing plasmid. Since the test article SNS-EF1/UU contains a human eIF5A siRNA that will not affect expression of the endogenous mouse eIF5A, another feature of this study was the inclusion of a group (Ex6-G6) that was dosed with PEI complexes containing a non-expressing plasmid and an siRNA that efficiently targets mouse eIF5A. This group allowed assessment of the safety of chronic administration of an active eIF5A siRNA.

All animals survived to the scheduled sacrifice date. No clinical signs of toxicity were observed in any of the groups over the course of the 9-week study and the mice in all groups continued to gain weight during the study period. Red and white blood cell counts were measured three and six weeks after the initiation of treatment and were normal for all dosing groups. Serum liver enzyme levels were measured following sacrifice and were within the normal range for all mice. No changes in the macroscopic appearance of the organs were observed in any of the groups. Histopathological analysis of the major organs was conducted by an independent pathologist (and revealed no toxicity attributable to the test article.

Chronic administration of therapeutic doses of SNS-EF1/UU is well tolerated by mice and no adverse effects were observed. In addition, chronic administration of a mouse-specific eIF5A siRNA revealed no toxic effects, indicating that the administration of PEI complexes containing a human eIF5A siRNA should be safe for humans.

Example 21

Therapeutic Efficacy Studies with Intra-Venous SNS-B29/UU and SNS01 in Multiple Myeloma Tumor-Bearing Mice

SNS01 is as described above. The test article SNS-B29/UU is a preclinical version of SNS01. SNS-B29/UU differs very little from SNS01, the chief difference being that the components are of research-grade rather than GLP-grade. The purpose of the study reported here was to determine the minimum effective dose of SNS-B29/UU and to confirm that the GLP-grade materials that comprise SNS01 perform as well as the research-grade materials that were used for the preclinical studies. The repeated dose tumor study (Study ID: EX9) was a 5-week study in which the ability of increasingly smaller twice-weekly doses of SNS-B29/UU to inhibit subcutaneous tumor growth in mice was assessed in order to determine the optimal therapeutic dose of SNS01. The treated animals were also assessed for signs of toxicity by monitoring clinical signs, body weight and organ weight.

Study		Injection	Duration of
ID	Animal Model	Schedule	Treatment	Test Article
Ex9	C.B17 (SCID)	Twice weekly	35 Days	SNS-B29/
	(female) mice	Intra-venous		UU
	bearing	Twice weekly	25 Days	SNS01
	subcutaneous	Intra-venous
	human multiple
	myeloma tumors
	(KAS-6/1)

Test				Material
Article	Plasmid DNA	siRNA	Vehicle	Grade
SNSOla	pExp5Ac	eIF5A siRNAd	In vivo-	GLP-
	(eIF5AK50R	(dTdT overhangc)	jetPEI ™	grade
	expression driven	human-specific		materials
	by B29 B-cell-	eIF5A siRNA
	specific promoter)
SNS-B29/	pExp5Ac	h5Al	In vivo-	Research-
UUb		(UU overhangc)	jetPEI ™	grade
		human-specific		materials
		eIF5A siRNA
aSNS01 contains GLP-grade materials and is being developed for the clinic
bSNS-B29/UU is a test article used in preclinical research that led to the development of SNS01
cthe pExp5A plasmid is RNAi-resistant due to the fact that the plasmid contains only the open reading frame of eIF5A while the eIF5A siRNA (h5A1) targets the 3′ UTR of eIF5A
dthe sequence of the eIF5A siRNA and the h5A1siRNAs are identical except for the presencee of a dTdT overhang rather than a UU overhang on the 3′ terminal ends of the siRNA; the dTdT overhang does not affect the target selectivity or efficacy of the siRNA but has been proposed to enhance stability

The therapeutic range of SNS-B29/UU was determined in SCID mice bearing subcutaneous human multiple myeloma tumors. Doses of SNS-B29/UU between 0.15 mg/kg and 1.5 mg/kg were tested. The anti-tumoral efficacy of the test article was determined by twice-weekly tumor volume measurements and by excising and weighing tumor tissue following sacrifice. SNS-B29/UU doses of 0.75 mg/kg and 1.5 mg/kg resulted in significant tumor shrinkage indicating that the therapeutic range of SNS-B29/UU lies between 0.75 mg/kg and 1.5 mg/kg. Effective inhibition of growth of subcutaneous tumors was also observed at 0.38 mg/kg SNS-B29/UU although no tumor shrinkage was observed. Some inhibition of tumor growth was even observed at doses as low as 0.15 mg/kg SNS-B29/UU indicating a broad therapeutic range. See FIGS. 26 and 27.

The efficacy of SNS01 made using GLP-grade components was compared to SNS-B29/UU and was found have a comparable efficacy in the inhibition of tumor growth. Treatment of tumor-bearing SCID mice with SNS01 and SNS-B29/UU was well tolerated and the mice continued to gain weight throughout the study.

Test Article and Vehicle

	Manufacturer
	of Plasmid	Manufacturer	Manufacturer
	DNA	of siRNA	of PEI	Formation of
Test Article	component	component	component	Test Article
SNS01	VGXI	Avecia	Polyplus	Components
	Lot #		Transfection	were combined
	pExp5A.08L007		Inc	with 10%
			GLP-Grade	glucose to form
				nano -
				complexes;
				complexes
				were injected
				within 2-4
				hours
SNS-B29/UU	Qiagen	ThermoScientific	Polyplus	Components
	EndoFree	Dharmacon	Transfection	were combined
	Plasmid Mega	RNAi	Inc.	with 10%
	Kit	Technologies	Research-	glucose to form
	<0.1 EU/μg		Grade	nano -
	DNA			complexes;
				complexes
				were injected
				within 2-4
				hours
Storage	−20° C.	−20°	4°	Room
Conditions	(≧1 year)	(≧1 year)	(≧1 year)	Temperature
(Stability)				(≧6 hours)

Test Systems and Study Design The female C.B.17/IcrHsd-Prkdc (SCID) mice were obtained from Harlan (Indianapolis,

IN, USA). Subcutaneous tumors were established by injecting 10×10⁶ viable KAS-6/1 (human multiple myeloma) cells into the right flank of 5 to 6 week-old mice. Treatment with SNS-B29/UU began when the tumors reached an approximate size of 20 to 40 mm³ (approximately 4 weeks after tumor cell injection). Treatment with SNS01 began when the tumors reached an approximate size of 130 mm³ (approximately 6 weeks after tumor cell injection). Mice received the test article twice-weekly via tail vein intra-venous injection.

STUDY ID: EX9
	No.
	Animals		N/P	Dose level	Injection	Total #
Group	(female)	Test Article	ratioa	(mg/kg)	Volume	injections
Ex9-G1	3	Controla	6	1.5 mg/kg	0.1 mL	11
Ex9-G2	4	SNS-	6	1.5 mg/kg	0.1 mL	11
		B29/UU
Ex9-G3	4	SNS-	6	0.75 mg/kg	0.05 mL	11
		B29/UU
Ex9-G4	4	SNS-	6	0.38 mg/kg	0.025 mL	11
		B29/UU
Ex9-G5	3	SNS-	6	0.15 mg/kg	0.01 mL	11
		B29/UU
Ex9-G9	3	SNS01	6	1.5 mg/kg	0.1 mL	7
aPEI complex containing a non-expressing plasmid (same vector background as pExp5A) and a non-targeting siRNA

Repeated Dose Tumor Study

The repeated dose tumor study was designed to determine the minimum effective therapeutic dose of SNS-B29/UU and to confirm that the GLP-grade SNS01 test article retained the tumor inhibition activity demonstrated by the research-grade test article SNS-B29/UU. A secondary objective was to assess any toxic effects of the treatment by monitoring the treated mice for clinical signs, body weight, and organ weight. Test article therapeutic anti-tumoral activity was monitored by twice-weekly tumor volume measurements using digital calipers. Upon sacrifice the tumors were excised and weighed.

All the mice survived to the scheduled sacrifice date. Control mice that were treated with PEI nanocomplexes containing a non-expressing plasmid and a non-targeting siRNA had an average tumor volume of 284 mm³ at the time of sacrifice while mice treated with 1.5 mg/kg SNS-B29/UU had an average tumor volume of only 13 mm³, a 95% (*p=0.026) reduction in tumor growth. However, when it was attempted to excise the tumors from mice that had been treated with 1.5 mg/kg SNS-B29/UU, no evidence of a tumor was found in any of the mice. Decreasing the dose of SNS-B29/UU by half to 0.75 mg/kg still resulted in a 91% (*p=0.03) and 87% (*p=0.04) decrease in tumor volume and weight, respectively, and in one mouse the tumor had completely disappeared. Therefore, the optimum therapeutic dose for twice-weekly injections of SNS-B29/UU appears to be between 0.75 mg/kg and 1.5 mg/kg. Twice-weekly doses of SNS-B29/UU doses as low as 0.15 mg/kg still resulted in a 60% reduction in the final tumor volume indicating that SNS-B29/UU has potent anti-tumoral activity over a wide dose range.

In addition to inhibiting tumor growth, treatment with SNS-B29/UU and SNS01 at 0.75 mg/kg and 1.5 mg/kg resulted in significant reduction in tumor volume indicating that this treatment is capable of inducing tumor regression, likely through the induction of apoptosis in the tumor. The percent change in tumor volume in tumor-bearing mice treated with SNS-B29/UU, at dose levels of 0.75 mg/kg and 1.5 mg/kg, was −244% and −245%, respectively. The tumors of control mice increased in size by more than 2000% during the same time period. Twice-weekly injections of SNS01 also significantly shrunk multiple myeloma tumors. The percent change in tumor volume for mice treated with 1.5 mg/kg SNS01 was −349%, indicating that SNS01 is just as effective as SNS-B29/UU. The use of GLP-grade materials may in fact have increased the biological activity since treatment with SNS01 achieved a 349% decrease in tumor volume following only 25 days of treatment while SNS-B29/UU achieved a 245% reduction in tumor volume following 35 days of treatment. In addition, the tumors treated with SNS01 were quite large (˜130 mm³) indicating that treatment with SNS01 is effective against well-established tumors.

The treatment was well tolerated by all mice and no clinical signs of toxicity were observed. The mice in all groups continued to gain weight throughout the study. No changes in the macroscopic appearance of the organs was observed at necropsy and no significant changes in the organ weight to body weight ratios occurred.

Therefore SNS01 (and its preclinical version SNS-B29/UU) is well tolerated by SCID mice and is extremely effective in treating subcutaneous human multiple myeloma tumors when delivered by intra-venous injection twice per week. All doses of SNS-B29/UU that were tested were effective at inhibiting tumor growth but the highest dose of 1.5 mg/kg successfully eliminated tumors in all mice receiving treatment.

Example 22

Biodistribution of Plasmid DNA and siRNA Polyethylenimine (JetPEI) Complexes

Green fluorescent protein (“GFP”)GFP-expression constructs were used to determine localization of plasmid DNA delivered by PEI complexes. Two promoters were used to drive GFP expression: EF1: ubiquitous promoter (EF1::GFP) or B29: B-cell specific promoter (B29::GFP). PEI complexes containing 20 micrograms of GFP plasmid DNA and 10 micrograms of a fluorescently-labelled (DY547) h5A1 siRNA were prepared at an N/P ratio of 6. BalB/C mice were injected intra-venously with either 5% glucose or PEI complexes on two consecutive days. Seventy-two hours following the firsts injection the mice were euthanized and their organs were harvested and analyzed for GFP expression and DY547-siRNA by confocal microscopy.

Bone Marrow:

In most cases there was evidence of DY547-siRNA but no GFP expression. Timing of organ harvest may not coincide with peak expression of GFP; and there may be quenching of GFP signal or GFP may not be expressed. However, GFP and DY547 that colocalized to the same bone marrow cells in some instances was observed. Therefore, this provides evidence that PEI nanoparticles can transfect bone marrow cells in a live animal when given by intra-venous injection

Lung:

In most cases there was evidence of DY547-siRNA but no GFP expression. Timing of organ harvest may not coincide with peak expression of GFP or there may be quenching of GFP signal or GFP may not be expressed.

Spleen:

Evidence of GFP expression (when driven by EF1 promoter) colocalizing in cells also positive for the presence of DY547-siRNA was seen. Expression of GFP was much lower in spleen cells when driven by the B29 promoter. This shows that PEI nanoparticles appear to transfect cells of the spleen.

Kidney:

No GFP or DY547 was observed indicating nanoparticles may not enter kidney. Liver: In most cases there was evidence of DY547-siRNA but no GFP expression. This provides evidence that PEI nanoparticles are transfecting cells of the liver.

Heart:

Colocalization of EF1::GFP and DY547-siRNA in tissue of heart was seen, thus indicating that PEI nanoparticles may be transfecting this organ. No GFP was observed with B29 promoter.

Example 23

Effect of DNA:siRNA Ratio on HA-eIF5A^K50R Expression

KAS cells were transfected with nanoparticles containing B29-HA-eIF5A^K50R (plasmid driven by B-cell-specific promoter) and h5A1 siRNA. JET PEI™ nanoparticles containing different ratios of pExp5A and h5A1 siRNA were made and incubated for 4 hours at room temperature prior to addition to KAS cells. Four hours after transfection, the nanoparticle-containing media was replaced with fresh media. Twenty-four hours later the cell lysate was harvested and used for western blot analysis with an antibody against HA. The ratio of DNA:siRNA was varied from the standard ratio of 2:1. The accumulation of HA-eIF5A^K50R peaked at ratios of 1:0, 3:1, and 2:1. See FIG. 30.

Example 24

Effect of DNA:siRNA Ratio on Apoptosis Induced by Nanoparticle Transfection

Nanoparticles containing different ratios of pExp5A and h5A1 siRNA were made and incubated for 4 hours at room temperature prior to addition to KAS cells. Four hours after transfection, the nanoparticle-containing media was replaced with fresh media. Forty-eight hours later the cells were harvested, labelled with Annexin V/PI and analyzed by FACS. The induction of apoptosis was highest in cells transfected with nanoparticles with the standard DNA:siRNA ratio of 2:1. See FIG. 31.

Example 25

Administration of PEI Complexes (N/P=6 or 8) Containing eIF5A1K50R Plasmid and eIF5A1 siRNA (siSTABLE or Non-siSTABLE) Inhibits Growth of Multiple Myeloma Subcutaneous Tumors and Results in Tumor Shrinkage

SCID mice were injected subcutaneously with KAS cells. Treatment was initiated when palpable tumors were observed. Mice were injected intra-venously 2 times per week with either: (G1) PEI complexes containing 20 mg of pCpG-mcs (empty vector) and 10 mg of control siRNA at N/P=8 (medium dose); (G5) PEI complexes containing 20 mg of the RNAi-resistant plasmid pCpG-eIF5A1k50R and 10 mg of siSTABLE h5A1 siRNA at N/P=8 (medium dose, siSTABLE); (G8) PEI complexes containing 20 mg of the RNAi-resistant plasmid pCpG-eIF5A1k50R and 10 mg of h5A1 siRNA at N/P=6 (medium dose, N/P=6). The data shown is the individual tumor volume for the mice in each group. The final injection was given at day 40 after initiation of treatment. See FIG. 32.

Example 26

JET PEI™ Nanoparticles are being Effectively Taken Up by Tumor Tissue and that Nanoparticles are Delivering Plasmid and siRNA to the Same Cell

Tumor section 48 hours after injection with nanoparticles containing pExp-GFP (GFP under control of B-cell-specific promoter) and DY547-siRNA (fluorescently-labelled siRNA). Co-localized expression of GFP and DY547 is observed in tumor section following confocal microscopy indicating that the nanoparticles are being effectively taken up by tumor tissue and that nanoparticles are delivering plasmid and siRNA to the same cell. See FIG. 33.

Example 27

Adenovirus Constructs Created for Truncation Study

Adenovirus (serotype 5, E3-deleted)

• • 1) Ad-eIF5A1A(2-6) [A(2-6)]—this is a human eIF5A1 lacking amino acids 2 to 6.
  • 2) Ad-eIF5A1K50RA(2-6) [A(2-6)/K50R] this is human eIF5A1 lacking amino acids 2 to 6. Additionally, the “K50R” means that the Lysine (K) at position 50 has been mutated to arginine (R) and is hence believed unable to by hypusinated by DHS.
  • 3) Ad-eIF5A1D6E [D6E]—this is human eIF5A1 in which the predicted cleavage site has been mutated (D6 to E).
  • 4) Ad-eIF5A1D6E/K50R [D6E/K50R]—this is human eIF5A1K50R in which predicted cleavage site has been mutated (D6 to E). Additionally, the “K50R” means that the Lysine (K) at position 50 has been mutated to arginine (R) and is hence believed unable to by hypusinated by DHS.

Example 28

Caspase Mediated Cleavage of eIF5A

To identify the site of cleavage, protein lysate isolated from KAS cells treated with Actinomycin D was separated by 2-D gel electrophoresis (FIG. 37) and the spot corresponding to the smaller molecular weight eIF5A cleavage product was cut out of the gel and sequenced by mass spectroscopy (FIG. 38B). Although a full-length sequence of the cleavage product was not obtained, it was determined that the cleavage occurred following the 6^th amino acid from the N-terminal end of the protein (FIG. 38A). The sequence immediately preceding the suspected cleavage site is ‘DDLD’, a sequence that has been identified as a caspase cleavage site (Chat′ et al., 2002).

To determine whether production of the cleavage fragment is caspase-dependent, the ability of caspase inhibitors to block the production of the cleavage fragment produced during Actinomycin D-induced apoptosis in human myeloma cells was tested (FIG. 41). A general caspase inhibitor and specific inhibitors of caspase 3, 8 and 9 all strongly prevent the formation of the cleavage form of eIF5A that accumulates during ActD-induced apoptosis in KAS cells. A caspase 1 inhibitor also reduced, but did not completely block, the formation of the cleavage product. Incubation with the caspase inhibitors not only prevented the accumulation of the cleavage product, but also inhibited loss of the hypusinated form of eIF5A (FIG. 41), indicating that loss of hypusinated eIF5A during Actinomycin D-induced apoptosis is a result of cleavage.

Caspase cleavage of proteins during apoptosis (reviewed by Fisher et al., 2003) can have a myriad of purposes: 1) to inactivate pro-survival or anti-apoptotic proteins—for example: the eukaryotic translation initiation factor 4G1, which binds to the 5′ cap structure of mRNAs and facilitates binding of capped mRNA to 40S ribosomal subunits, is inactivated by caspase cleavage, thereby inhibiting translation; 2) to create a dominant negative form of the protein (for example, NF-kappa B p65 is cleaved by caspases during apoptosis to create a dominant-negative fragment that binds DNA but has no trans-activating activity and therefore acts as a dominant-negative inhibitor of NF-kB); 3) gain-of-function cleavage resulting in the activation of a pro-apoptotic protein by removal of an inhibitory or regulatory domain thereby resulting in formation of a fragment with a new activity or increased activity (for example, BRCA-1, a breast cancer suppressor protein that mediates cell cycle arrest and apoptosis, is activated by caspase cleavage which releases a pro-apoptotic cleavage fragment. DAPS, a member of the eIF4G family is activated following caspase cleavage; the cleavage product stimulates translation of apoptosis-related proteins); 4) conversion of an anti-apoptotic protein to a pro-apoptotic protein (for example, apoptotic inhibitors, such as Bcl-xL and c-IAP1, can be turned into pro-apoptotic proteins through cleavage by caspase); and 5) cellular redistribution (for example, upon cleavage by caspase 8, the pro-apoptotic p15 fragment of Bid undergoes myristoylation at a glycine residue exposed by cleavage which subsequently enables Bid to translocate to the mitochondria where it enhances cytochrome c release).

To determine whether caspase-mediated cleavage of eIF5A during Actinomycin D-induced apoptosis is a general phenomena or specific to myeloma cells, HeLa cells treated with Actinomycin D were examined for the presence of cleaved eIF5A (FIG. 42). No accumulation of the eIF5A cleavage fragment was observed in Actinomycin D-treated HeLa cells. In an effort to determine whether post-translation modification (such as phosphorylation or acetylation) of eIF5A may be a pre-requisite for cleavage by caspases, the effect of a deacetylase inhibitor, nicotinamide, on the formation of the cleavage fragment was examined. Acetylation of eIF5A has been observed by mass spectroscopy analysis of eIF5A by our lab and others (Kim et al., 2006). Furthermore, yeast eIF5A has been identified as a substrate of the Sir2-related deacetylase Hst2 (Shirai et al., 2008) and the authors observed that acetylation of eIF5A was only observed in yeast lacking Hst2 or in yeast in which eIF5A was over-expressed, indicating that eIF5A is generally present in the unacetylated form. Incubation of Actinomycin D-treated HeLa cells with the Sir2 deacetylase inhibitor nicotinamide, resulted in the accumulation of the eIF5A cleavage product indicating that acetylation of eIF5A is required for caspase-mediated cleavage to occur. These data suggest that eIF5A may normally be protected from caspase activity until an apoptotic signal triggers acetylation of eIF5A and allows caspase-mediated cleavage.

REFERENCES

• Chay K O, Park S S, Mushinski J F (2002). Linkage of caspase-mediated degradation of paxillin to apoptosis in Ba/F3 murine pro-B lymphocytes. J Biol Chem. 277, 1452114529.
• Fischer U, Janicke R U, Schulze-Osthoff K (2003). Many cuts to ruin: a comprehensive update of caspase substrates. Cell Death and Differentiation 10, 76-100.
• Kim, S. C., Sprung, R., Chen, Y., Xu, Y., Ball, H., Pei, J., Cheng, T., Kho, Y., Xiao, H., Xiao, L., Grishin, N. V., White, M., Yang, X. J., and Zhao, Y. (2006) Substrate and Functional Diversity of Lysine Acetylation Revealed by a Proteomics Survey. Mol Cell 23, 607-618.
• Shirai et al. (2008). Global analysis of gel mobility of proteins and its use in target identification J. Biol. Chem. 283, 10745-10752.

Claims

1-57. (canceled)

58. An isolated eIF5A1 polypeptide consisting of (a) the amino acid sequence set forth in SEQ ID NO: 37 or (b) the amino acid sequence of amino acids 7-154 of SEQ ID NO: 35 except that the amino acid sequence of SEQ ID NO: 35 has at least one of the following mutations K50A, K50R, K67A, K47R, K67R, K50A/K67A, K50A/K47R, K50A/K67R, K50R/K67A, K50R/K47R, K50R/K67R, or K47A/K67A.

59. A method for inducing apoptosis in a cancer cell or in a tumor in a subject, the method comprising administering the isolated polypeptide of claim 58.

60. The method of claim 58 further comprising administering a full length eIF5A1 polypeptide to the subject.

61. The method of claim 60 wherein the full length eIF5A1 polypeptide comprises the amino acid sequence set forth in SEQ ID NO: 35.

62. The method of claim 59 wherein the subject is a mammal.

63. The method of claim 62 wherein the mammal is a human.

64. The method of claim 59 wherein the induction of apoptosis slows cancer cell or tumor growth, arrests cancer cell or tumor cell growth, or kills cancer cells or reduces tumor size.

65. The method of claim 59 wherein the cancer is multiple myeloma.

66. The method of claim 60 further comprising an siRNA targeted against the 3′UTR of eIF5A1.

67. The method of claim 66 wherein the siRNA targets the sequence in eIF5A1 of 5′-GCT GGA CTC CTC CTA CAC A-3′ (SEQ ID NO: 45).

68. The method of claim 67 where in the siRNA is dsRNA and one strand of the dsRNA comprises the sequence of 5′-GCU GGA CUC CUC CUA CAC A-3′ (SEQ ID NO: 46).

69. The method of claim 67 wherein the siRNA is stabilized to prevent degradation in serum.

70. The method of claim 59 wherein the composition is administered intravenously, intraperitoneally or intratumorally.