GPX4
脂质过氧化
程序性细胞死亡
细胞凋亡
DNA损伤
癌症研究
诱导剂
癌细胞
氧化应激
细胞生物学
化学
生物
癌症
生物化学
DNA
遗传学
基因
超氧化物歧化酶
谷胱甘肽过氧化物酶
作者
Ling F. Ye,Kunal Chaudhary,Fereshteh Zandkarimi,Andrew Harken,Connor J. Kinslow,Pavan S. Upadhyayula,Athanassios Dovas,Dominique Higgins,Hui Tan,Yan Zhang,Manuela Buonanno,Tony J. C. Wang,Tom K. Hei,Jeffrey N. Bruce,Peter Canoll,Simon K. Cheng,Brent R. Stockwell
标识
DOI:10.1021/acschembio.9b00939
摘要
Although radiation is widely used to treat cancers, resistance mechanisms often develop and involve activation of DNA repair and inhibition of apoptosis. Therefore, compounds that sensitize cancer cells to radiation via alternative cell death pathways are valuable. We report here that ferroptosis, a form of nonapoptotic cell death driven by lipid peroxidation, is partly responsible for radiation-induced cancer cell death. Moreover, we found that small molecules activating ferroptosis through system xc– inhibition or GPX4 inhibition synergize with radiation to induce ferroptosis in several cancer types by enhancing cytoplasmic lipid peroxidation but not increasing DNA damage or caspase activation. Ferroptosis inducers synergized with cytoplasmic irradiation, but not nuclear irradiation. Finally, administration of ferroptosis inducers enhanced the antitumor effect of radiation in a murine xenograft model and in human patient-derived models of lung adenocarcinoma and glioma. These results suggest that ferroptosis inducers may be effective radiosensitizers that can expand the efficacy and range of indications for radiation therapy.
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