Found in translation-Fibrosis in metabolic dysfunction-associated steatohepatitis (MASH)

被引:37
|
作者
Wang, Shuang [1 ]
Friedman, Scott L. [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Div Liver Dis, New York, NY 10029 USA
关键词
NONALCOHOLIC FATTY LIVER; HEPATIC STELLATE CELLS; SINUSOIDAL ENDOTHELIAL-CELLS; KILLER T-CELLS; GROWTH-FACTOR; ADIPOSE-TISSUE; MOUSE MODELS; CONFERS SUSCEPTIBILITY; OSTEOPONTIN EXPRESSION; DISEASE PROGRESSION;
D O I
10.1126/scitranslmed.adi0759
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Metabolic dysfunction-associated steatohepatitis (MASH) is a severe form of liver disease that poses a global health threat because of its potential to progress to advanced fibrosis, leading to cirrhosis and liver cancer. Recent advances in single-cell methodologies, refined disease models, and genetic and epigenetic insights have provided a nuanced understanding of MASH fibrogenesis, with substantial cellular heterogeneity in MASH livers providing potentially targetable cell-cell interactions and behavior. Unlike fibrogenesis, mechanisms underlying fibrosis regression in MASH are still inadequately understood, although antifibrotic targets have been recently identified. A refined antifibrotic treatment framework could lead to noninvasive assessment and targeted therapies that preserve hepatocellular function and restore the liver's architectural integrity.
引用
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页数:22
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