Targeting ferroptosis, a novel programmed cell death, for the potential of alcohol-related liver disease therapy

被引:12
|
作者
Shi, Jing-Fen [1 ,2 ,3 ]
Liu, Yu'e [4 ]
Wang, Yan [3 ]
Gao, Ru [3 ]
Wang, Yi [5 ]
Liu, Jun [3 ,6 ]
机构
[1] Univ Elect Sci & Technol China, Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Inst Hlth Policy, Chengdu, Peoples R China
[2] Univ Elect Sci & Technol China, Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Hosp Management, Chengdu, Peoples R China
[3] Wenjiang Dist Peoples Hosp Chengdu, Chengdu, Peoples R China
[4] Tongji Univ, Shanghai Peoples Hosp 10, Sch Med, Canc Ctr, Shanghai, Peoples R China
[5] Univ Elect Sci & Technol China, Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Dept Crit Care Med, Chengdu, Peoples R China
[6] Univ Elect Sci & Technol China, Sichuan Acad Med Sci & Sichuan Prov Peoples Hosp, Dept Ultrasound Med, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
ferroptosis; ALD; ROS; GPx4; p53; ferroptosis inducers; ferroptosis inhibitors; HEPATIC IRON OVERLOAD; VITAMIN-E; UP-REGULATION; INHIBITION; EXPRESSION; MECHANISM; LIPROXSTATIN-1; FERROSTATIN-1; PEROXIDATION; PATHOGENESIS;
D O I
10.3389/fphar.2023.1194343
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ferroptosis is a new iron-dependent cell death mode, which is different from the other types of programmed cell death, such as apoptosis, necrosis, and autophagy. Ferroptosis is characterized by a process in which fatal lipids from lipid peroxidation accumulate in cells and eventually lead to cell death. Alcohol-related liver disease (ALD) is a type of liver injury caused by excessive alcohol intake. Alcohol-related liver disease is a broad-spectrum disease category, which includes fatty liver, steatohepatitis, hepatitis, cirrhosis, and hepatocellular tumors. Recent studies have found that ferroptosis is involved in the pathological development of non-viral liver diseases. Therefore, ferroptosis may be an ideal target for the treatment of non-viral liver diseases. In this review article, we will elaborate the molecular mechanism and regulatory mechanism of ferroptosis, explore the key role of ferroptosis in the Alcohol-related liver disease process, and summarize the existing targeted ferroptosis drugs and their feasibility for the treatment of Alcohol-related liver disease.
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页数:10
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