目的:探讨法尼醇x受体(FXR)表达对人肝癌细胞SMMC-7721细胞增殖的影响及分子机制。方法:在人正常肝细胞株L02、肝癌细胞株Hep3B和SMMC-7721中检测FXR的表达;分别采用FXR激动剂GW4064和抑制剂INT747干预FXR的表达,通过CCK-8实验检测FXR表达改变对SMMC-7721细胞株细胞增殖的影响;进一步用WB检测参与FXR表达改变对Akt信号通路的影响。结果:WB结果显示较L02,FXR在Hep3B和SMMC-7721表达降低;CCK-8结果提示在SMMC-7721细胞中,FXR表达增高降低细胞增殖(p〈O.05),反之则促进细胞的生长和活性(P〈O.05);V413结果显示FXR表达改变能负调节Akt的表达。结论:FXR可能通过Akt信号通路调节人肝癌细胞SMMC-7721的细胞增殖。
Objective: To investigate the effect of farnesoid X receptor (FXR) expression on the proliferation of human hepatoma cell line SMMC-7721 and related molecular mechanism. Methods: The expression of FXR was measuredin the normal humanliver cells L02 and hepatoma cell lines Hep3B and SMMC-7721. An FXR agonist GW4064 and an FXR inhibitor INT747 were used to interfere with the expression of FXR. Cell Counting Kit-8 (CCK-8)was used to investigate the effect of the change in FRX expression on the proliferation of SMMC- 7721 cells, and Western blot was used to analyze the effect of the change in FRX expression on the Akt signaling pathway. Results: The results of Western blot showed that Hep3B and SMMC-7721 cells had lower FXR expression than L02 cells.CCK-8 showed thatincreased FXR expression significantly reduced the proliferation of SMMC-7721 cells (P 〈 0.05), while a reduction in FXR expression significantly increased the growth and viability of cells. Western blot also showed that the change in FXR expression negatively regulated the expression of Akt. Conclusions: FXR regulates theproliferation ofhuman hepatoma SMMC-7721cellsvia the Akt signaling pathway.