疾病
GPX4
程序性细胞死亡
生物
神经科学
医学
细胞凋亡
氧化应激
遗传学
病理
生物化学
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Carsten Berndt,Hamed Alborzinia,Vera Skafar Amen,Scott Ayton,Uladzimir Barayeu,Alexander Bartelt,Hülya Bayır,Christina M. Bebber,Kıvanç Birsoy,Jan P. Böttcher,Simone Brabletz,Thomas Brabletz,Ashley R. Brown,Bernhard Brüne,Giorgia Bulli,Alix Bruneau,Quan Chen,Gina M. DeNicola,Tobias P. Dick,Ayelén Mariana Distefano
出处
期刊:Redox biology
[Elsevier BV]
日期:2024-05-30
卷期号:75: 103211-103211
被引量:55
标识
DOI:10.1016/j.redox.2024.103211
摘要
Ferroptosis is a pervasive non-apoptotic form of cell death highly relevant in various degenerative diseases and malignancies. The hallmark of ferroptosis is uncontrolled and overwhelming peroxidation of polyunsaturated fatty acids contained in membrane phospholipids, which eventually leads to rupture of the plasma membrane. Ferroptosis is unique in that it is essentially a spontaneous, uncatalyzed chemical process based on perturbed iron and redox homeostasis contributing to the cell death process, but that it is nonetheless modulated by many metabolic nodes that impinge on the cells' susceptibility to ferroptosis. Among the various nodes affecting ferroptosis sensitivity, several have emerged as promising candidates for pharmacological intervention, rendering ferroptosis-related proteins attractive targets for the treatment of numerous currently incurable diseases. Herein, the current members of a Germany-wide research consortium focusing on ferroptosis research, as well as key external experts in ferroptosis who have made seminal contributions to this rapidly growing and exciting field of research, have gathered to provide a comprehensive, state-of-the-art review on ferroptosis. Specific topics include: basic mechanisms, in vivo relevance, specialized methodologies, chemical and pharmacological tools, and the potential contribution of ferroptosis to disease etiopathology and progression. We hope that this article will not only provide established scientists and newcomers to the field with an overview of the multiple facets of ferroptosis, but also encourage additional efforts to characterize further molecular pathways modulating ferroptosis, with the ultimate goal to develop novel pharmacotherapies to tackle the various diseases associated with - or caused by - ferroptosis.
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