MicroRNAs in the pathogenesis and treatment of progressive liver injury in NAFLD and liver fibrosis

被引:98
|
作者
Su, Qiaozhu [1 ]
Kumar, Virender [2 ]
Sud, Neetu [1 ]
Mahato, Ram I. [2 ]
机构
[1] Univ Nebraska, Dept Nutr & Hlth Sci, 316F Leverton Hall, Lincoln, NE 68583 USA
[2] Univ Nebraska Med Ctr, Dept Pharmaceut Sci, Omaha, NE 68198 USA
关键词
NAFLD; NASH; Liver fibrosis; Lipotoxicity; Metabolic inflammation; miRNAs; AntimiRNAs; NONALCOHOLIC FATTY LIVER; HEPATIC STELLATE CELLS; ENDOPLASMIC-RETICULUM STRESS; CIRCULATING MICRORNAS; INSULIN-RESISTANCE; HEDGEHOG INHIBITOR; OXIDATIVE STRESS; LIPID-METABOLISM; GENE-EXPRESSION; DISEASE;
D O I
10.1016/j.addr.2018.01.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Non-alcoholic fatty liver disease (NAFLD) increases the risk of various liver injuries, ranging from simple steatosis to non-alcoholic steatohepatitis (NASH), fibrosis and cirrhosis, and ultimately hepatocellular carcinoma (HCC). Ample evidence has suggested that aberrant expression of microRNAs (miRNAs) is functionally involved in the activation of cellular stress, inflammation and fibrogenesis in hepatic cells, including hepatocytes, Kupffer and hepatic stellate cells (HSCs), at different pathological stages of NAFLD and liver fibrosis. Here, we overview recent findings on the potential role of miRNAs in the pathogenesis of NAFLD, including lipotoxicity, oxidative stress, metabolic inflammation and fibrogenesis. We critically assess the literatures on both human subjects and animal models of NAFLD and liver fibrosis with miRNA dysregulation and their mechanisms of actions in liver damage. We further highlight the potential use of miRNA mimics or antimiRNAs as therapeutic approaches for the prevention and treatment of NAFLD and liver fibrosis. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:54 / 63
页数:10
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