Department of Pathology, Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Xiangya Hospital, Central South University, Changsha, 410078, Hunan, China.
NHC Key Laboratory of Carcinogenesis (Central South University), Cancer Research Institute and School of Basic Medicine, Central South University, Changsha, 410078, Hunan, China.
Mol Cancer. 2020 Feb 27;19(1):39. doi: 10.1186/s12943-020-01157-x.
Ferroptosis, a novel form of regulated cell death, is different from other types of cell death in morphology, genetics and biochemistry. Increasing evidence indicates that ferroptosis has significant implications on cell death linked to cardiomyopathy, tumorigenesis, and cerebral hemorrhage to name a few. Here we summarize current literature on ferroptosis, including organelle dysfunction, signaling transduction pathways, metabolic reprogramming and epigenetic regulators in cancer progression. With regard to organelles, mitochondria-induced cysteine starvation, endoplasmic reticulum-related oxidative stress, lysosome dysfunction and golgi stress-related lipid peroxidation all contribute to induction of ferroptosis. Understanding the underlying mechanism in ferroptosis could provide insight into the treatment of various intractable diseases including cancers.
铁死亡是一种新的细胞程序性死亡形式,在形态、遗传和生物化学上与其他类型的细胞死亡不同。越来越多的证据表明,铁死亡对与心肌病、肿瘤发生和脑出血等相关的细胞死亡有重要影响。在这里,我们总结了目前关于铁死亡的文献,包括细胞器功能障碍、信号转导通路、代谢重编程和癌症进展中的表观遗传调节剂。就细胞器而言,线粒体诱导的半胱氨酸饥饿、内质网相关的氧化应激、溶酶体功能障碍和高尔基体应激相关的脂质过氧化都有助于铁死亡的诱导。了解铁死亡的潜在机制可以为治疗包括癌症在内的各种难治性疾病提供新的思路。