Radiation-Induced Lipid Peroxidation Triggers Ferroptosis and Synergizes with Ferroptosis Inducers

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
出处
期刊:ACS Chemical Biology [American Chemical Society]
卷期号:15 (2): 469-484 被引量:393
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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