Department of Liver Surgery, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Int J Med Sci. 2021 Jul 25;18(15):3361-3366. doi: 10.7150/ijms.62903. eCollection 2021.
Ferroptosis is an iron-dependent form of regulated cell death, which is characterized by a large amount of lipid peroxide accumulation and the imbalance of redox state in cells. Ferroptosis is usually accompanied with the dysfunction of lipid repair enzyme (glutathione peroxidase 4, GPX4), large masses of iron accumulation and lipid peroxidation of polyunsaturated fatty acids (PUFAs). Ferroptosis is related to several signaling pathways, including amino acid and iron metabolism, ferritinophagy, cell adhesion and p53 and Keap1/Nrf2 signaling pathways. A number of studies have indicated that ferroptosis is closely associated with acute renal failure, tumor, ischemia and reperfusion injury, neurodegenerative diseases and liver fibrosis. Liver fibrosis, which has long been a global health problem, still lacks effective treatment till now, and the discovery of ferroptosis provides a new insight into addressing this issue.
铁死亡是一种依赖铁的细胞程序性死亡方式,其特征是细胞内大量脂质过氧化物的积累和氧化还原状态的失衡。铁死亡通常伴随着脂质修复酶(谷胱甘肽过氧化物酶 4,GPX4)功能障碍、大量铁积累和多不饱和脂肪酸(PUFAs)的脂质过氧化。铁死亡与几种信号通路有关,包括氨基酸和铁代谢、铁蛋白自噬、细胞黏附和 p53 以及 Keap1/Nrf2 信号通路。许多研究表明,铁死亡与急性肾衰竭、肿瘤、缺血再灌注损伤、神经退行性疾病和肝纤维化密切相关。肝纤维化一直是一个全球性的健康问题,到目前为止仍然缺乏有效的治疗方法,而铁死亡的发现为解决这一问题提供了新的思路。