GPX4
脂质过氧化
抗氧化剂
程序性细胞死亡
体内
化学
癌症研究
生物化学
细胞凋亡
癌症
细胞生物学
癌细胞
生物
生物技术
过氧化氢酶
遗传学
谷胱甘肽过氧化物酶
作者
Chenyao Wu,Zhonglong Liu,Zhixin Chen,Deliang Xu,Lisong Chen,Han Lin,Jianlin Shi
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2021-09-22
卷期号:7 (39): eabj8833-eabj8833
被引量:246
标识
DOI:10.1126/sciadv.abj8833
摘要
-phosphomolybdic acid nanosheet (CPMNS)–enabled lipid peroxide (LOOH) accumulation via accelerated Mo(V)-Mo(VI) transition, elevated GSH depletion for GPX4 enzyme deactivation, and ROS burst, for efficient ferroptosis and chemotherapy. Both in vitro and in vivo outcomes demonstrate the notable anticancer ferroptosis efficacy, suggesting the high feasibility of this CPMNS-enabled ferroptosis-like therapeutic concept. It is highly expected that such ferroptosis-like design in nanocatalytic medicine would be beneficial to future advances in the field of cancer-therapeutic regimens.
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