Met may be a promising1 personalized treatment method for approximately 45 percent of patients with hepatocellular carcinoma (HCC肝细胞癌) who have c-Met-positive tumors, according to study results presented at the Fourth AACR International Conference on Molecular3 Diagnostics in Cancer Therapeutic4 Development. HCC is the most common primary malignant5(恶性的,有害的) tumor2 of the liver; c-Met is a receptor for hepatocyte(肝细胞) growth factor that appears to drive liver cancer growth, invasion and metastasis(转移,新陈代谢) .
"Current therapies for HCC patients are ' one size fits all(一刀切,一体适用) .' We propose that molecular profiling will enable better therapy for HCC patients with a c-Met positive tumor," said Hanning You, M.D., Ph.D., postdoctoral fellow working in the laboratory of C. Bart Rountree, M.D., in the departments of pediatrics(小儿科) and pharmacology(药物学) , at the Pennsylvania State University College of Medicine, Hershey, Pa.
Using a preclinical translational study to validate6 c-Met as a target for HCC, You and colleagues found c-Met was highly overexpressed in metastatic(转移性的) liver cancer cells.
"By targeting c-Met we were able to suppress tumor growth in vivo(在活体内) and kill these metastatic liver cancer cells," said You.
Since c-Met inhibitor stopped proliferation and tumor growth of metastatic HCC cells, the researchers concluded that c-Met might be a potential personalized target of metastatic HCC. In addition, they found that results of a separate meta-analysis of six studies and 1,051 patients showed that c-Met activation7 is associated with poor prognosis in HCC.