摘要
脂质过氧化驱动的铁依赖的铁死亡是一种受调控的细胞死亡机制,涉及许多疾病,如神经系统疾病、肾损伤、缺血和肿瘤,包括前列腺癌。铁死亡的细胞机制与铁、活性氧和氨基酸代谢途径密切相关。 几种化合物,即铁死亡诱导剂,通过 i)抑制 Xc - 转运系统,ii)削弱 GPX4 功能和 iii) 氧化铁和多不饱和磷脂,影响这些途径并引发铁死亡。 临床前研究表明,与常规抗癌药物联合使用,铁死亡诱导剂对前列腺癌和对抗去势抵抗性疾病的进展有效。 本综述概述了与铁死亡有关的机制,并讨论了在前列腺癌中的研究结果。
关键词: 前列腺癌,铁死亡,脂质过氧化,GPX4, ROS,癌症治疗。
Current Medicinal Chemistry
Title:Ferroptosis Inducers for Prostate Cancer Therapy
Volume: 29 Issue: 24
关键词: 前列腺癌,铁死亡,脂质过氧化,GPX4, ROS,癌症治疗。
摘要: Lipid peroxidation-driven iron-dependent ferroptosis is a regulated cell death mechanism implicated in numerous diseases, such as neurological diseases, kidney injury, ischemia, and tumors, including prostate cancer. The cellular mechanisms of ferroptosis are strongly associated with iron, reactive oxygen species and amino acid metabolic pathways. Several compounds, namely ferroptosis inducers, impact these pathways and trigger ferroptosis by i) inhibiting Xc - transporter system, ii) impairing GPX4 functions and iii) oxidizing iron and polyunsaturated phospholipids. Preclinical studies show 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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Cite this article as:
Ferroptosis Inducers for Prostate Cancer Therapy, Current Medicinal Chemistry 2022; 29 (24) . https://dx.doi.org/10.2174/0929867329666220111120924
DOI https://dx.doi.org/10.2174/0929867329666220111120924 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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