Compositions, kits, and methods for identification, assessment, prevention, and therapy of cancer
The invention relates to compositions, kits, and methods for detecting, characterizing, preventing, and treating human cancer. A variety of chromosomal regions (MCRs) and markers corresponding thereto, are provided, wherein alterations in the copy number of one or more of the MCRs and/or alterations in the amount, structure, and/or activity of one or more of the markers is correlated with the presence of cancer.
1. A method of assessing the efficacy of a test compound for inhibiting multiple myeloma in a subject, the method comprising:
a) determining the amount and/or activity of a protein marker in a first sample comprising multiple myeloma cells obtained from the subject and maintained in the presence of the test compound, wherein the protein marker is selected from the group consisting of PRKCi protein, SEMA4A protein, DHX36 protein, and combinations thereof;
b) determining the amount and/or activity of the protein marker in a second sample comprising multiple myeloma cells obtained from the subject and maintained in the absence of the test compound; and
c) comparing the amount and/or activity of the protein marker in the first subject sample to the amount and/or activity of the protein marker in the second subject sample;
wherein a significantly lower amount and/or activity of the protein marker in the first sample relative to the second sample is an indication that the test compound is efficacious for inhibiting multiple myeloma.
2. The method of claim 1 , wherein the first and second samples are portions of a single sample obtained from the subject.
3. The method of claim 1 , wherein the first and second samples are portions of pooled samples obtained from the subject.
4. The method of claim 1 , wherein the marker is PRKCi.
5. The method of claim 1 , wherein the marker is SEMA4A.
6. The method of claim 1 , wherein the marker is DHX36.
7. The method of claim 1 , wherein the first subject sample and/or the second subject sample is selected from the group consisting of tissue, whole blood, serum, plasma, buccal scrape, saliva, cerebrospinal fluid, urine, stool, and bone marrow.
8. The method of claim 7 , wherein the first subject sample and/or the second subject sample comprise plasma cells.
9. The method of claim 1 , wherein the presence of the protein is detected using a reagent which specifically binds with the protein.
10. The method of claim 9 , wherein the reagent is selected from the group consisting of an antibody, an antibody derivative, and an antibody fragment.