Objective: To investigate the differential expression of serum-and-glucocorticoid-inducible-kinase-2 (SGK2) in
hepatocellular carcinoma (HCC) and normal liver tissues and the related mechanism mediating signal transduction of
GSK-3 β / β
catenin in HCC cells. Methods: Twenty pairs of matched HCC and normal tissues were collected and the situation of expression of SGK2
mRNA was detected by real-time fluorescence quantitative PCR. Western blot was used to detect the levels of SGK2
protein in human HCC cell lines (Huh-7, SMMC-7721) and normal human liver cell line (L02). SGK2
siRNA was used to transfect human HCC cell lines (SMMC-7721 and Huh-7), and then the
protein expression levels of
GSK-3 β/ β -
catenin was successfully detected with the above-mentioned transfected cell line by western blot. Measurement data were expressed as mean ± standard deviation (x±s), and the Student t -test was used as the statistical method. Results: SGK2
mRNA expression was up-regulated in all 20 HCC samples than that of the expression of matched normal liver tissues. SGK2
protein levels were significantly higher in Huh-7 and SMMC-7721 than normal human liver cell lines (P < 0.01). The downregulation of SGK2 expression in human HCC cell lines (SMMC-7721 and Huh-7) had inhibited the expression of unphosphorylated
GSK-3 β. In addition, the downregulation of SGK2 expression in HCC cell lines had decreased the dephosphorylation of β -
catenin to prevent degradation of the β -
catenin proteasome. Conclusion: SGK2 is overexpressed in HCC and mediates GSK-3β/β-
catenin signaling in HCC cells.