Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10815665 | Cellular Signalling | 2012 | 10 Pages |
Abstract
⺠PPARγ is a pivotal molecular in hepatic stellate cell activation and liver fibrosis. ⺠PPARγ interacts with signal pathways mediated by growth factors and adipokines. ⺠PPARγ modulates apoptosis and senescence implicated in liver fibrogenesis. ⺠These molecular insights update PPARγ biology and understanding of hepatic fibrosis. ⺠Drug targets for antifibrotic therapy may derive from PPARγ-mediated mechanisms.
Keywords
ObRperoxisome-proliferator activated receptorNF-κB-inducing kinaseJAK2TLREGR-1TGF-βSA-β-galPDGFTNFHGFECMAdipoRSMP30CHBAP1LXR-αperoxisome proliferator response elementsTRAIL-RTβRNIKJanus Kinase 2PPARHSCliver X receptor-αJnkPI3KNF-κBSREBP-1cSTAT3Sirt1AMPKCTGFERKC/EBPc-Jun N-terminal kinaseMAPKsenescence-associated β-galactosidasePPREtransforming growth factor-βtransforming growth factor-β receptorToll-like receptorHepatic stellate cellHepatocyte growth factorConnective tissue growth factorplatelet-derived growth factortumor necrosis factornuclear factor-κBphosphatidylinositol-3-kinaseLiver fibrosisExtracellular matrixsignal transducer and activator of transcription 3cross-regulationSignal transductionchronic hepatitis Bearly growth response-1CCAAT/enhancer binding proteinactivator protein 1senescence marker protein 305′-AMP-activated protein Kinasemitogen-activated protein kinaseCideaextracellular signal-regulated kinaseadiponectin receptordeath receptorPeroxisome proliferator-activated receptor-γ
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Authors
Feng Zhang, Yin Lu, Shizhong Zheng,