GPX4
放射增敏剂
脂质过氧化
癌症研究
放射治疗
细胞内
活性氧
肿瘤微环境
谷胱甘肽
细胞生物学
谷胱甘肽过氧化物酶
抗氧化剂
化学
生物
医学
生物化学
肿瘤细胞
内科学
酶
作者
Ying Liu,Fen Pi,Lizhen He,Fang Yang,Tianfeng Chen
出处
期刊:Small
[Wiley]
日期:2024-03-20
卷期号:20 (32): e2310118-e2310118
被引量:26
标识
DOI:10.1002/smll.202310118
摘要
also triggers the ferroptosis and promotes the accumulation of lipid peroxides. Subsequently, the depletion of glutathione and accumulation of lipid peroxidation in tumor cells leads to the inactivation of glutathione peroxidase 4 (GPX4) and ferroptosis, thereby enhancing the therapeutic efficacy of radiotherapy. The nanoplatform provides a novel strategy for generating novel nanomedicines for ferroptosis-assisted radiotherapy.
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