A panel of molecular markers in hepatitis c virus-related hepatocellular carcinoma

Background : Hepatocellular carcinoma is triggered by many factors including infection with hepatitis C virus. The molecular basis, however, of the development of HCV-related HCC remains unknown. Objective : This work was designated to compare the circulating levels of some molecular markers between HCV-infected and HCV-free HCC patients. Methods : We investigated 77 of HCC patients admitted to the National Cancer Institute, Cairo during the period 2002-2003. The plasma circulating levels of bcl-2, transforming growth factor beta 1 (TGF-ß1), vascular endothelial growth factor (VEGF) and beta2-microglobulin (ß2- MG) were investigated in HCV related HCC patients (n = 40) compared to both HCV-free HCC patients (n = 37) and a group of healthy subjects (n = 20). Additionally, the LOH at the mannose 6-phosphate / insulin like growth factor-II receptor (M6P / IGFIIr) was investigated. Results : The result did not predict a significant role of HCV infection on the circulating bcl-2 protein. In both HCC and HCC / HCV groups a limited number of patients had high levels of bcl-2. TGF-ß1 level increased particularly, but insignificantly in HCC associated with HCV infection. A similar pattern was obtained in the levels of ß2-MG, however the difference between HCC and HCC / HCV patients was significant (p = 0.001). The infection with HCV was associated with a high incidence of LOH at M6P / IGFIIr site compared to HCV-free patients. Although the level of serum VEGF was significantly higher in all HCC patients than in healthy control, no significant difference, however was observed between HCV infected and HCV-free groups. Conclusion : In HCC patients, HCV infection did not exclusively affect the levels of both bcl-2 and VEGF. TGF-ß1, ß2-MG and the LOH at M6P/IGFIIr, however were higher in presence of HCV infection.