Ferroptosis in Different Pathological Contexts Seen through the Eyes of Mitochondria

线粒体 谷胱甘肽 生物 表型 程序性细胞死亡 细胞内 病态的 细胞生物学 细胞凋亡 抗氧化剂 GPX4 脂质过氧化 医学 谷胱甘肽过氧化物酶 生物化学 病理 基因
作者
Vesna Otašević,Milica Vučetić,Ilijana Grigorov,Vanja Martinović,Ana Stančić
出处
期刊:Oxidative Medicine and Cellular Longevity [Hindawi Limited]
卷期号:2021: 1-16 被引量:52
标识
DOI:10.1155/2021/5537330
摘要

Ferroptosis is a recently described form of regulated cell death characterized by intracellular iron accumulation and severe lipid peroxidation due to an impaired cysteine-glutathione-glutathione peroxidase 4 antioxidant defence axis. One of the hallmarks of ferroptosis is a specific morphological phenotype characterized by extensive ultrastructural changes of mitochondria. Increasing evidence suggests that mitochondria play a significant role in the induction and execution of ferroptosis. The present review summarizes existing knowledge about the mitochondrial impact on ferroptosis in different pathological states, primarily cancer, cardiovascular diseases, and neurodegenerative diseases. Additionally, we highlight pathologies in which the ferroptosis/mitochondria relation remains to be investigated, where the process of ferroptosis has been confirmed (such as liver- and kidney-related pathologies) and those in which ferroptosis has not been studied yet, such as diabetes. We will bring attention to avenues that could be followed in future research, based on the use of mitochondria-targeted approaches as anti- and proferroptotic strategies and directed to the improvement of existing and the development of novel therapeutic strategies.
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