GPX4, ferroptosis, and diseases

被引:39
|
作者
Zhang, Wangzheqi [1 ]
Liu, Yang [1 ]
Liao, Yan [1 ]
Zhu, Chenglong [1 ]
Zou, Zui [1 ]
机构
[1] Naval Med Univ, Sch Anesthesiol, 168 Changhai Rd, Shanghai 200433, Peoples R China
关键词
GPX4; Ferroptosis; Sepsis; Nervous system diseases; Ischemia reperfusion injury; Cardiovascular diseases; Cancer; GLUTATHIONE-PEROXIDASE; 4; CELL-DEATH; REPERFUSION INJURY; OXIDATIVE STRESS; NUCLEAR FORM; EXPRESSION; PROTEIN; CANCER; IDENTIFICATION; SEPSIS;
D O I
10.1016/j.biopha.2024.116512
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
GPX4 (Glutathione peroxidase 4) serves as a crucial intracellular regulatory factor, participating in various physiological processes and playing a significant role in maintaining the redox homeostasis within the body. Ferroptosis, a form of iron-dependent non-apoptotic cell death, has gained considerable attention in recent years due to its involvement in multiple pathological processes. GPX4 is closely associated with ferroptosis and functions as the primary inhibitor of this process. Together, GPX4 and ferroptosis contribute to the pathophysiology of several diseases, including sepsis, nervous system diseases, ischemia reperfusion injury, cardiovascular diseases, and cancer. This review comprehensively explores the regulatory roles and impacts of GPX4 and ferroptosis in the development and progression of these diseases, with the aim of providing insights for identifying potential therapeutic strategies in the future.
引用
收藏
页数:15
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