| Literature DB >> 25268046 |
Yajun Wang1, Jun Wu2, Biyun Lin3, Xv Li3, Haitao Zhang4, Hang Ding3, Xiaoyi Chen3, Liubo Lan3, Hui Luo5.
Abstract
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.Entities:
Keywords: Autophagy; Autophagy-related gene; Galangin; Smad; TGF-β receptor
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Year: 2014 PMID: 25268046 DOI: 10.1016/j.tox.2014.09.010
Source DB: PubMed Journal: Toxicology ISSN: 0300-483X Impact factor: 4.221