GPX4
前列腺癌
脂质过氧化
癌症研究
癌症
诱导剂
前列腺
活性氧
药理学
程序性细胞死亡
医学
化学
生物
氧化应激
细胞凋亡
生物化学
内科学
超氧化物歧化酶
基因
谷胱甘肽过氧化物酶
作者
Nadia Zaffaroni,Giovanni Luca Beretta
标识
DOI:10.2174/0929867329666220111120924
摘要
Lipid peroxidation-driven iron-dependent ferroptosis is a regulated cell death mechanism implicated in numerous disease, such as neurological diseases, kidney injury, ischemia, and tumors, including prostate cancer. The cellular mechanisms of ferrosptosis are strongly associated with iron, reactive oxygen species and aminoacid metabolic pathways. Several compounds, namely ferroptosis inducers, impact on these pathways and trigger ferroptosis by i) inhibiting Xc- transporter system, ii) impairing GPX4 functions and iii) oxidizing iron and polyunsaturated phospholipids. Preclinical studies showed that in combination with conventional anticancer drugs, ferroptosis inducers are effective in prostate cancer and in combating the progression towards the castration resistant disease. This review overviews the mechanisms implicated in ferroptosis and discusses the findings achieved in prostate cancer.
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