Galangin suppresses HepG2 cell proliferation by activating the TGF-β receptor/Smad pathway.

نویسندگان

  • Yajun Wang
  • Jun Wu
  • Biyun Lin
  • Xv Li
  • Haitao Zhang
  • Hang Ding
  • Xiaoyi Chen
  • Liubo Lan
  • Hui Luo
چکیده

Galangin can suppress hepatocellular carcinoma (HCC) cell proliferation. In this study, we demonstrated that galangin induced autophagy by activating the transforming growth factor (TGF)-β receptor/Smad pathway and increased TGF-β receptor I (RI), TGF-βRII, Smad1, Smad2, Smad3 and Smad4 levels but decreased Smad6 and Smad7 levels. Autophagy induced by galangin appears to depend on the TGF-β receptor/Smad signalling pathway because the down-regulation of Smad4 by siRNA or inhibition of TGF-β receptor activation by LY2109761 blocked galangin-induced autophagy. The down-regulation of Beclin1, autophagy-related gene (ATG) 16L, ATG12 and ATG3 restored HepG2 cell proliferation and prevented galangin-induced apoptosis. Our findings indicate a novel mechanism for galangin-induced autophagy via activation of the TGF-β receptor/Smad pathway. The induction of autophagy thus reflects the anti-proliferation effect of galangin on HCC cells.

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عنوان ژورنال:
  • Toxicology

دوره 326  شماره 

صفحات  -

تاریخ انتشار 2014