How do different lipid peroxidation mechanisms contribute to ferroptosis?

被引:11
作者
Do, Quynh [1 ,2 ]
Xu, Libin [1 ]
机构
[1] Univ Washington, Dept Med Chem, 1959 NE Pacific St, Seattle, WA 98195 USA
[2] Partner Therapeut, 2625 162 nd St SW, Lynnwood, WA 98087 USA
来源
CELL REPORTS PHYSICAL SCIENCE | 2023年 / 4卷 / 12期
基金
美国国家卫生研究院;
关键词
POLYUNSATURATED FATTY-ACIDS; ABSOLUTE RATE CONSTANTS; CELL-DEATH; HYDROCARBON AUTOXIDATION; UNSATURATED COMPOUNDS; OXIDATION; IDENTIFICATION; CHEMISTRY; KINETICS; TUMOR;
D O I
10.1016/j.xcrp.2023.101683
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lipid peroxidation is the driver of ferroptotic cell death. However, nonconjugated and conjugated polyunsaturated fatty acids poten-tiate ferroptosis differently, while some isoprenoid-derived lipids inhibit ferroptosis despite being highly oxidizable. In this perspec-tive, we propose that different oxidation mechanisms and products contribute to the discrepancies in the lipids' potency in modulating ferroptosis. We first discuss the relative reactivities of various lipids toward two rate-determining free radical propagating mechanisms, hydrogen atom transfer (HAT) and peroxyl radical addition (PRA), and the resulting differential product profiles. We then discuss the role and regulation of lipid peroxidation in ferroptosis and the po-tential contributions of different oxidation products, such as trun-cated lipids and lipid electrophiles, from HAT and PRA mechanisms to the execution of ferroptosis. Lastly, we offer our perspective on the remaining questions to fully understand the process from lipid peroxidation to ferroptosis.
引用
收藏
页数:13
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