Epigenetic Mechanisms in Hepatic Stellate Cell Activation During Liver Fibrosis and Carcinogenesis

被引:56
作者
Barcena-Varela, Marina [1 ]
Colyn, Leticia [1 ]
Fernandez-Barrena, Maite G. [1 ,2 ,3 ]
机构
[1] Univ Navarra, CIMA, Hepatol Program, Pamplona 31180, Spain
[2] Inst Salud Carlos III, CIBERehd, Madrid 28029, Spain
[3] Inst Invest Sanitarias Navarra IdiSNA, Pamplona 31180, Spain
关键词
Tumor microenvironment; fibrosis; hepatic stellate cells; epigenetic remodeling; HISTONE DEACETYLASE INHIBITOR; GENE-EXPRESSION PROFILE; DNA METHYLATION; MYOFIBROBLAST TRANSDIFFERENTIATION; MATRIX METALLOPROTEINASES; COLLAGEN-SYNTHESIS; HEPATOCELLULAR-CARCINOMA; GUADECITABINE SGI-110; SIGNALING PATHWAY; TRICHOSTATIN-A;
D O I
10.3390/ijms20102507
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Liver fibrosis is an essential component of chronic liver disease (CLD) and hepatocarcinogenesis. The fibrotic stroma is a consequence of sustained liver damage combined with exacerbated extracellular matrix (ECM) accumulation. In this context, activation of hepatic stellate cells (HSCs) plays a key role in both initiation and perpetuation of fibrogenesis. These cells suffer profound remodeling of gene expression in this process. This review is focused on the epigenetic alterations participating in the transdifferentiation of HSCs from the quiescent to activated state. Recent advances in the field of DNA methylation and post-translational modifications (PTM) of histones (acetylation and methylation) patterns are discussed here, together with altered expression and activity of epigenetic remodelers. We also consider recent advances in translational approaches, including the use of epigenetic marks as biomarkers and the promising antifibrotic properties of epigenetic drugs that are currently being used in patients.
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页数:16
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