Ferroptosis: Iron-mediated cell death linked to disease pathogenesis

被引:0
|
作者
Zhang, Xiangyu [1 ]
Hu, Yingchao [1 ]
Wang, Bingwei [2 ]
Yang, Shuo [1 ]
机构
[1] Nanjing Med Univ, Wuxi Peoples Hosp, Collaborat Innovat Ctr Personalized Canc Med, Wuxi Med Ctr,Gusu Sch,Dept Immunol,State Key Lab R, Nanjing 211166, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Dept Pharmacol, 138 Xianlin Ave, Nanjing 210023, Jiangsu, Peoples R China
来源
JOURNAL OF BIOMEDICAL RESEARCH | 2024年 / 38卷 / 05期
基金
中国博士后科学基金;
关键词
ferroptosis; lipid peroxidation; molecular regulatory mechanisms; ferroptosis-related diseases; ferroptosis inducers; ferroptosis inhibitors; LIPID-PEROXIDATION; DEPENDENT MANNER; OXIDATIVE STRESS; FATTY-ACIDS; TGF-BETA; MECHANISMS; GPX4; FERROSTATIN-1; TEMOZOLOMIDE; PROTECTS;
D O I
10.7555/JBR.37.20230224
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Ferroptosis is a pattern of iron-mediated regulatory cell death characterized by oxidative damage. The molecular regulatory mechanisms are related to iron metabolism, lipid peroxidation, and glutathione metabolism. Additionally, some immunological signaling pathways, such as the cyclic GMP-AMP synthase-stimulator of the interferon gene axis, the Janus kinase-signal transducer and activator of transcription 1 axis, and the transforming growth factor beta 1-Smad3 axis, may also participate in the regulation of ferroptosis. Studies have shown that ferroptosis is significantly associated with many diseases such as cancer, neurodegenerative diseases, inflammatory diseases, and autoimmune diseases. Considering the pivotal role of ferroptosis-regulating signaling in the pathogenesis of diverse diseases, the development of ferroptosis inducers or inhibitors may have significant clinical potential for the treatment of aforementioned conditions.
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页数:24
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