Cell Death and Cell Death Responses in Liver Disease: Mechanisms and Clinical Relevance

被引:843
作者
Luedde, Tom [1 ]
Kaplowitz, Neil [2 ]
Schwabe, Robert F. [3 ,4 ]
机构
[1] Univ Hosp RWTH Aachen, Dept Med 3, D-52074 Aachen, Germany
[2] Univ So Calif, Keck Sch Med, Div Gastrointestinal & Liver Dis, Los Angeles, CA 90033 USA
[3] Columbia Univ, Dept Med, New York, NY 10032 USA
[4] Columbia Univ, Inst Human Nutr, New York, NY 10032 USA
关键词
Apoptosis; Necrosis; Necroptosis; Necrosome; DAMP; Viral Hepatitis; NASH; Clinical Trial; Hepatocellular Carcinoma; Alcoholic Liver Disease; DILI; Caspases; RIP3; RIP Kinases; MITOCHONDRIAL PERMEABILITY TRANSITION; HEPATITIS-C VIRUS; NF-KAPPA-B; SERUM AMINOTRANSFERASE CONCENTRATION; ENDOPLASMIC-RETICULUM STRESS; ACUTE ALCOHOLIC HEPATITIS; DOMAIN-LIKE PROTEIN; GROUP BOX-1 PROTEIN; NONALCOHOLIC STEATOHEPATITIS; HEPATOCELLULAR-CARCINOMA;
D O I
10.1053/j.gastro.2014.07.018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Hepatocellular death is present in almost all types of human liver disease and is used as a sensitive parameter for the detection of acute and chronic liver disease of viral, toxic, metabolic, or autoimmune origin. Clinical data and animal models suggest that hepatocyte death is the key trigger of liver disease progression, manifested by the subsequent development of inflammation, fibrosis, cirrhosis, and hepatocellular carcinoma. Modes of hepatocellular death differ substantially between liver diseases. Different modes of cell death such as apoptosis, necrosis, and necroptosis trigger specific cell death responses and promote progression of liver disease through distinct mechanisms. In this review, we first discuss molecular mechanisms by which different modes of cell death, damage-associated molecular patterns, and specific cell death responses contribute to the development of liver disease. We then review the clinical relevance of cell death, focusing on biomarkers; the contribution of cell death to drug-induced, viral, and fatty liver disease and liver cancer; and evidence for cell death pathways as therapeutic targets.
引用
收藏
页码:765 / U110
页数:23
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