Abstract: The present invention provides a set of methods and compositions for homogeneous coupled luminescent assays of cytotoxicity and/or proliferation of cells, as well as for enzymatic activity. In both cases the activities of the enzymes of interest are coupled to production of a high-energy molecule, which serves as a substrate for the production of light by a luciferase, typically in a single reagent mixture, with a useful readout available in 1—5 minutes. Individual cytotoxicity and proliferation signals can be measured from a single sample in 6 minutes or less. The invention also provides a 3-minute, one-step phosphatase assay. The ability to couple the activity of interest to light production in a one-step procedure gives rise to extremely rapid and flexible methods for measurement of cytotoxic effects and enzymatic activities. The assay methods are highly suitable for use in high-throughput screening procedures.

Abstract: Methods of screening for and/or detecting the presence or absence of cancers or treating cancers are described. In an aspect of the present invention, the screening methods are based on the detection of the PAL-18 protein, variants thereof, or a nucleic acid molecules encoding the same, found to be associated with the presence of cancer. Additional methods for imaging using antibodies for PAL-18 or modulating PAL-18 are provided. Preferred embodiments to the methods include detection based on immunological properties, physical properties, enzymatic properties and combinations thereof, or detection of a nucleic acid molecule encoding antigen (e.g., PAL-18) based on nucleic acid amplification.