Hepatitis B virus X protein promotes hepatoma cell proliferation via upregulation of MEKK2

Aim:To investigate the mechanism underlying the increase of hepatoma cell proliferation by hepatitis B virus X protein (HBx).Methods:Hep G2, H7402 and Hep G2.2.15 cells, which constitutively replicated hepatitis B virus were used. The effects of HBx on hepatoma cell proliferation were examined using 5-ethynyl-2-deoxyuridine (Ed U) incorporation assay and MTT assay. The expression level of MEKK2 was measured using RT-PCR, Western blot and luciferase reporter gene assay. The activity of activator protein 1 (AP-1) was detected using luciferase reporter gene assay. The phosphorylation levels of JNK and c-Jun were measured using Western blot. The expression levels of HBx and MEKK2 in 11 clinical hepatocellular carcinoma (HCC) tissues were measured using real time PCR and Western blot. In addition, the expression of MEKK2 in 95 clinical HCC tissues was examined using immunohistochemistry.Results:HBx significantly enhanced Hep G2-X cell proliferation. In Hep G2-X, H7402-X and Hep G2.2.15 cells, the expression level of MEKK2 was remarkably increased. In Hep G2.2.15 cells, HBx was found to activate JNK and AP-1, which were the downstream effectors of MEKK2 in Hep G2-X and Hep G2.2.15 cells. In 11 clinical HCC tissues, both HBx and MEKK2 expression levels were remarkably increased, as compared to those in the corresponding peritumor tissues. In 95 clinical HCC tissues, the rate of detection of MEKK2 was 85.3%.Conclusion:HBx promotes hepatoma cell proliferation via upregulating MEKK2, which may be involved in hepatocarcinogenesis.