Non-alcoholic steatohepatitis: emerging molecular targets and therapeutic strategies

被引:326
|
作者
Musso, Giovanni [1 ]
Cassader, Maurizio [2 ]
Gambino, Roberto [2 ]
机构
[1] Gradenigo Hosp, Corso Regina Margherita 8, I-10132 Turin, Italy
[2] Univ Turin, Dept Med Sci, Corso AM Dogliotti 14, I-10126 Turin, Italy
关键词
FATTY LIVER-DISEASE; HEPATIC STELLATE CELLS; FARNESOID-X-RECEPTOR; NLRP3 INFLAMMASOME ACTIVATION; ENDOPLASMIC-RETICULUM STRESS; GROWTH-FACTOR; 21; DIACYLGLYCEROL ACYLTRANSFERASE 2; IMPROVES INSULIN-RESISTANCE; ADIPOSE-TISSUE INFLAMMATION; UNFOLDED PROTEIN RESPONSE;
D O I
10.1038/nrd.2015.3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Non-alcoholic fatty liver disease - the most common chronic liver disease encompasses a histological spectrum ranging from simple steatosis to non-alcoholic steatohepatitis (NASH). Over the next decade, NASH is projected to be the most common indication for liver transplantation. The absence of an effective pharmacological therapy for NASH is a major incentive for research into novel therapeutic approaches for this condition. The current focus areas for research include the modulation of nuclear transcription factors; agents that target lipotoxicity and oxidative stress; and the modulation of cellular energy homeostasis, metabolism and the inflammatory response. Strategies to enhance resolution of inflammation and fibrosis also show promise to reverse the advanced stages of liver disease.
引用
收藏
页码:249 / 274
页数:26
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