Abstract: Systems, methods, and computer readable media for diagnosing or characterizing epithelial cancer or its stages based on the level of expression of the Wnt5a gene or protein are provided. The level of nucleic acids encoding Wnt5a or the level of Wnt5a protein is measured in a tissue sample, and the level is compared with reference values. Methods for inducing senescence of an epithelial cancer cell are also provided.
Type:
Application
Filed:
August 9, 2013
Publication date:
December 5, 2013
Applicant:
Institute for Cancer Research d/b/a The Research Institute of Fox Chase Cancer Center ("Fox Chase
Abstract: The invention provides methods for enhancing the cytotoxicity of DNA damage in cancer cells that express thymine DNA glycosylase, and treating tumors accordingly. The methods comprise inhibiting the expression or biologic activity of thymine DNA glycosylase, and inducing DNA damage in the cancer cells. DNA damage may be induced by administration of bendamustine or gemcitabine to the cancer cells.
Type:
Application
Filed:
March 15, 2013
Publication date:
November 14, 2013
Applicant:
Institute for Cancer Research d/b/a The Research Institute of Fox Chase Cancer Center
Inventor:
Institute for Cancer Research d/b/a The Research Institute of Fox Chase Cancer Center
Abstract: Anti-EGFR family member antibodies and bispecific antibodies comprising one or more anti-EGFR family member antibodies are disclosed. These antibodies can be used to advantage to specifically target forms of cancer associated with the overexpression of members of the EGFR protein family.
Type:
Grant
Filed:
November 20, 2007
Date of Patent:
November 12, 2013
Assignees:
The Regents of the University of California, Fox Chase Cancer Center
Inventors:
Gregory P. Adams, Eva M. Horak, Louis M. Weiner, James D. Marks
Abstract: Methods for inhibiting the motility or proliferation of premalignant and malignant cells are provided. Methods for treating a malignancy of the head and neck and for treating a malignancy of the lung are also provided.
Type:
Application
Filed:
November 30, 2011
Publication date:
September 26, 2013
Applicant:
Institute For Cancer Research d/b/a The Research Institute of Fox Chase Cancer Center ("Fox Chase
Inventors:
Margie L. Clapper, Ekaterina G. Shatalova, Sibele Meireles
Abstract: A nasal cannula adapter. The nasal cannula adapter includes a chamber having cannula clips, and a connector having an opening and a connector lumen in communication with the chamber and the opening. Systems for administering a gas to a patient comprise the nasal cannula adapter, a nasal cannula, and an airway device. Methods for administering a gas to a patient comprise administering a gas through a nasal cannula operably connected to the nasal cannula adapter operably connected to an airway device inserted into the airway of the patient.
Type:
Application
Filed:
November 22, 2011
Publication date:
September 19, 2013
Applicant:
Institute for Cancer Research d/b/a The Research Center of Fox Chase Cancer Center ("Fox Chase Canc
Abstract: Treatment of lymphangioleiomyomatosis with the MEK1/2 inhibitor CI-1040 delayed the development of primary tumors and blocked the estrogen-induced lung metastases in treated animals. Such treatment also reduced the number of circulating ELT3 cells and decreased their lung colonization after intravenous injection.
Abstract: Bispecific single chain antibody molecules are disclosed which may be used to advantage to treat various forms of cancer associated with the overexpression of members of the EGFR protein family.
Type:
Application
Filed:
December 10, 2012
Publication date:
August 8, 2013
Applicants:
Fox Chase Cancer Center, The Regents of the University of California
Inventors:
The Regents of the University of California, Fox Chase Cancer Center
Abstract: Disclosed is a class of compounds which inhibit the enzymatic conversion of fructose-lysine into fructose-lysine-3-phosphate in an ATP dependent reaction in a newly discovered metabolic pathway. According to the normal functioning on this pathway, fructose-lysine-3-phosphate (FL3P) is broken down to form free lysine, inorganic phosphate and 3-deoxyglucosone (3DG), the latter being a reactive protein modifying agent. 3DG can be detoxified by reduction to 3-deoxyfructose (3DF), or it can react with endogenous proteins to form advanced glycation end-product modified proteins (AGE-proteins) Also disclosed are therapeutic methods of using such inhibitors to alleviate deleterious effects of 3DG.
Abstract: This relates to the prevention of cancer initiation. More specifically, the invention provides compositions and methods useful for altering the genetic signature in breast tissue, said alteration being correlated with a reduced risk for the development of breast cancer.
Abstract: Antibodies that specifically bind to an epitope on the extracellular domain of TEM7R are provided. Nucleic acids encoding such antibodies and cells capable of expressing such antibodies are also provided. The antibodies may be used in methods for treating tumors and for inhibiting angiogenesis in tumors.
Abstract: The invention provides a natural killer cell, NK-92, modified to express an Fc receptor on the surface of the cell, such as CD16 (Fc?RIII-A), or other Fc? or Fc receptors. The modified NK-92 cell can be further modified to concurrently express an associated accessory signaling protein, such as Fc?RI-?, TCR-?, or to concurrently express interleukin-2 (IL-2) or other cytokines. Additional methods are disclosed for various assays, assessments, and therapeutic treatments with the modified NK-92 cells.
Abstract: A method of affecting a multimeric protein comprising an equilibrium of assembly states, each assembly having a plurality of units, wherein each of the units comprises a first complementary surface and a second complementary surface and wherein the first complementary surface of one unit is associated with the second complementary surface of another unit, provided that the assembly is at least one of different quaternary isoforms under four conditions, wherein the method comprising: applying to the multimeric protein a composition comprising a compound adapted to affect formation of an active form of the multimeric protein; associating the composition with an active form of the multimeric protein; and promoting the multimeric protein to assemble into the active form, thereby affecting the multimeric protein to form the active form, wherein the multimeric protein is phenylalanine hydroxylase.
Abstract: Methods for altering pancreatic and liver cell function are provided, wherein the compositions and methods are based on use of netrin-4 or on altering the activity of netrin-4.
Abstract: Bispecific single chain antibody molecules are disclosed which may be used to advantage to treat various forms of cancer associated with the overexpression of members of the EGFR protein family.
Type:
Grant
Filed:
November 20, 2007
Date of Patent:
December 11, 2012
Assignees:
The Regents of the University of California, Fox Chase Cancer Center
Inventors:
Gregory P. Adams, Eva M. Horak, Louis M. Weiner, James D. Marks
Abstract: The invention provides a natural killer cell, NK-92, modified to express an Fc receptor on the surface of the cell, such as CD16 (Fc?RIII-A), or other Fc? or Fc receptors. The modified NK-92 cell can be further modified to concurrently express an associated accessory signaling protein, such as Fc?RI-?, TCR-?, or to concurrently express interleukin-2 (IL-2) or other cytokines. Additional methods are disclosed for various assays, assessments, and therapeutic treatments with the modified NK-92 cells.
Abstract: Methods for inhibiting estrogen hormone-induced pulmonary metastasis of smooth muscle cells that are capable of pulmonary metastasis comprise antagonizing the estradiol receptor on the smooth muscle cells such that pulmonary metastasis of the cells is inhibited.
Abstract: The energy of positive ions accelerated in laser-matter interaction experiments can be significantly increased by providing a plurality of laser pulses, e.g., through the process of splitting the incoming laser pulse, to form multiple laser-matter interaction stages. From a thermodynamic point of view, the splitting procedure can be viewed as an effective way of increasing the efficiency of energy transfer from the laser light to positive ions, which energy peaks for processes having the least amount of entropy gain. A 100% increase in the energy efficiency is achieved for a six-stage laser positive ion accelerator compared to a single-stage laser positive ion accelerator.
Type:
Grant
Filed:
November 13, 2008
Date of Patent:
September 18, 2012
Assignee:
Fox Chase Cancer Center
Inventors:
Chang-ming Ma, Iavor Veltchev, Eugene S. Fourkal