Zhang Bei, Li Luyao, Wang Nan, Zhu Zixuan, Wang Mingyang, Tan Wu Peng, Liu Jianfeng, Zhou Shouhong
Guangxi Key Laboratory of Brain and Cognitive Neuroscience, Guilin Medical College, Guilin 541199, China; Basic Medical College, Guilin Medical College, Guilin 541199, China.
Department of Gynaecology, Maternal and Child Health Hospital of Hengyang, Hengyang 421001, China.
Int J Biol Macromol. 2025 Jan;285:138143. doi: 10.1016/j.ijbiomac.2024.138143. Epub 2024 Nov 30.
Protein arginine methyltransferases (PRMTs) play an essential role in the regulation of ferroptosis, a form of programmed cell death characterized by abnormal iron ion metabolism, lipid peroxidation, and DNA damage. Through methylation, PRMTs modify specific proteins, thereby altering their activity, localizations, or interactions with other molecules to control the ferroptosis process. This study was conducted to provide a comprehensive overview of the relationship between PRMTs and ferroptosis, with a focus on the mechanisms by which PRMTs regulate ferroptosis and their effect on this cell death pathway. Currently, only a few studies have been conducted on the regulation of ferroptosis by PRMTs. However, this review provides insights into the effects of PRMTs on ferroptosis regulators, suggesting that the regulation of ferroptosis by PRMTs holds potential as a new therapeutic target for related diseases.
蛋白质精氨酸甲基转移酶(PRMTs)在铁死亡的调控中起着至关重要的作用。铁死亡是一种程序性细胞死亡形式,其特征为异常的铁离子代谢、脂质过氧化和DNA损伤。通过甲基化作用,PRMTs修饰特定蛋白质,从而改变其活性、定位或与其他分子的相互作用,以控制铁死亡过程。本研究旨在全面概述PRMTs与铁死亡之间的关系,重点关注PRMTs调节铁死亡的机制及其对这一细胞死亡途径的影响。目前,关于PRMTs对铁死亡的调控仅开展了少数研究。然而,本综述深入探讨了PRMTs对铁死亡调节因子的影响,表明PRMTs对铁死亡的调控有望成为相关疾病的新治疗靶点。