疾病
医学
GPX4
背景(考古学)
癌症
癌症研究
发病机制
免疫学
氧化应激
生物
病理
内科学
古生物学
过氧化氢酶
谷胱甘肽过氧化物酶
作者
Junyi Chen,Yang Xiang,Xuexian Fang,Fudi Wang,Junxia Min
出处
期刊:PubMed Central
[National Institutes of Health]
日期:2020-05-25
卷期号:49 (1): 44-57
被引量:10
标识
DOI:10.3785/j.issn.1008-9292.2020.02.24
摘要
Recently, ferroptosis, an iron-dependent novel type of cell death, has been characterized as an excessive accumulation of lipid peroxides and reactive oxygen species. Emerging studies demonstrate that ferroptosis not only plays an important role in the pathogenesis and progression of chronic diseases, but also functions differently in the different disease context. Notably, it is shown that activation of ferroptosis could potently inhibit tumor growth and increase sensitivity to chemotherapy and immunotherapy in various cancer settings. As a result, the development of more efficacious ferroptosis agonists remains the mainstay of ferroptosis-targeting strategy for cancer therapeutics. By contrast, in non-cancerous chronic diseases, including cardiovascular & cerebrovascular diseases and neurodegenerative diseases, ferroptosis functions as a risk factor to promote these diseases progression through triggering or accelerating tissue injury. As a matter of fact, blocking ferroptosis has been demonstrated to effectively prevent ischemia-reperfusion heart disease in preclinical animal models. Therefore, it is a promising field to develope potent ferroptosis inhibitors for preventing and treating cardiovascular & cerebrovascular diseases and neurodegenerative diseases. In this article, we summarize the most recent progress on ferroptosis in chronic diseases, and draw attention to the possible clinical impact of this recently emerged ferroptosis modalities.
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