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ABSTRACT: Background
Ginsenoside Rg1, a bioactive component of Ginseng, has demonstrated anti-inflammatory, anti-cancer, and hepatoprotective effects. It is known that the epithelial-mesenchymal transition (EMT) plays a key role in the activation of hepatic stellate cells (HSCs). Recently, Rg1 has been shown to reverse liver fibrosis by suppressing EMT, although the mechanism of Rg1-mediated anti-fibrosis effects is still largely unclear. Interestingly, Smad7, a negative regulator of the transforming growth factor β (TGF-β) pathway, is often methylated during liver fibrosis. Whether Smad7 methylation plays a vital role in the effects of Rg1 on liver fibrosis remains unclear.Methods
Anti-fibrosis effects were examined after Rg1 processing in vivo and in vitro. Smad7 expr
SUBMITTER: Zhang R
PROVIDER: S-EPMC10310870 | biostudies-literature | 2023 Jul
REPOSITORIES: biostudies-literature