ASSAY FOR PREDICTION OF RESPONSE TO MET ANTAGONISTS
A method for classifying cancer patients as likely to have lower response to MET receptor antagonist therapy comprises assessment of the presence or absence of a single nucleotide polymorphism in the MET promoter in a patient tissue sample. The invention provides more effective identification of patients to receive MET receptor antagonist therapy.
1 . A method for classifying a patient as likely to exhibit lower response to anti-MET-receptor therapy comprising: (a) providing a tissue sample from a patient; (b) determining MET promoter allele presence or absence in the patient tissue sample, wherein the MET promoter allele comprises a rs185830-C single nucleotide polymorphism ; and (c) classifying the patient as likely to exhibit lower response to anti-MET receptor therapy where the patient's sample is determined to comprise the rs185830-C polymorphism.
2 . The method of claim 1 wherein the tissue sample is a peripheral blood sample from a patient with a cancer selected from the group consisting of bladder, breast , cervical, colorectal, esophageal, gastric, head and neck, kidney, liver, lung, nasopharyngeal, ovarian, pancreas, gall bladder, prostate and thyroid carcinoma; muscoskeletal sarcoma including osteosarcoma, synovial sarcoma, and rhabdomyosarcoma; soft tissue sarcoma including fibrososarcoma, leiomyosarcoma and Kaposi's sarcoma; hematopoetic malignancy including multiple myeloma, lymphoma, and adult T-cell leukemia; glioblastoma; astroycytoma; melanoma; mesothelioma; and Wilm's tumor.
3 . The method of claim 1 wherein the tissue sample is a peripheral blood sample from a patient with a cancer.
4 . The method of claim 3 wherein the cancer is an epithelial cell based cancer.
5 . The method of claim 1 wherein the MET promoter allele presence or absence is determined by a nucleic acid based assay using a pair of amplification primers comprising: t, 22
6 . The method of claim 1 wherein the MET promoter allele is located on human chromosome 7, between nucleotides 41495741 and 41496392.
7 . The method of claim 1 wherein the anti-MET receptor therapy comprises a small molecule inhibitor of MET, a small molecule inhibitor of HCF, an antibody inhbitor of MET, an antibody inhibitor of HCF, an siRNA inhibitor of MET, or an siRNA inhibitor of HCF.
8 . The method of claim 5 wherein the MET promoter allele presence or absence is determined by real-time polymerase chain reaction using a pair of detector probes comprising the following sequences: CGCTGGGCTCAGCCGGG (SEQ. ID. NO. 4) and CTGGGCTCAGCCCGGCC (SEQ. ID. NO. 5).
9 . A method for classifying a patient as likely to exhibit lower response to anti-MET-receptor therapy based on presence of a rs185830-C allele comprising: (a) providing a blood sample from a cancer patient; (b) extracting chromosomal DNA from the blood sample; (c) amplifying the chromosomal DNA by polymerase chain reaction using nucleic acid primers of sequence GATTTCCCTCTGGGTGGTG (SEQ. ID. NO. 2), and CAAGCCCCATTCTAGTTTCG (SEQ. ID. NO. 3) to produce an amplified DNA sample; and (d) determining presence or absence of a rs185830-C allele in the amplified DNA sample.
10 . The method of claim 9 , wherein the presence or absence of the rs185830 allele is determined by real-time PCR.
11 . The method of claim 10 wherein a pair of detector probes comprising the following sequences: CGCTGGGCTCAGCCGGG (SEQ. ID. NO. 4) and CTGGGCTCAGCCCGGCC (SEQ. ID. NO. 5), are used.