蛋氨酸
GPX4
脂质过氧化
半胱氨酸
谷胱甘肽
生物化学
反硫化
体内
化学
胶质瘤
谷胱甘肽过氧化物酶
抗氧化剂
程序性细胞死亡
脂质代谢
胱硫醚β合酶
半胱氨酸代谢
生物
癌症研究
氨基酸
酶
细胞凋亡
生物技术
作者
Pavan S. Upadhyayula,Dominique Higgins,Angeliki Mela,Matei A. Banu,Athanassios Dovas,Fereshteh Zandkarimi,Purvi Patel,Aayushi Mahajan,Nelson Humala,Trang Nguyen,Kunal Chaudhary,Lillian Liao,Michael Argenziano,Tejaswi Sudhakar,Colin Sperring,Benjamin L. Shapiro,Eman R. Ahmed,Connor J. Kinslow,Ling F. Ye,Markus D. Siegelin
标识
DOI:10.1038/s41467-023-36630-w
摘要
Ferroptosis is mediated by lipid peroxidation of phospholipids containing polyunsaturated fatty acyl moieties. Glutathione, the key cellular antioxidant capable of inhibiting lipid peroxidation via the activity of the enzyme glutathione peroxidase 4 (GPX-4), is generated directly from the sulfur-containing amino acid cysteine, and indirectly from methionine via the transsulfuration pathway. Herein we show that cysteine and methionine deprivation (CMD) can synergize with the GPX4 inhibitor RSL3 to increase ferroptotic cell death and lipid peroxidation in both murine and human glioma cell lines and in ex vivo organotypic slice cultures. We also show that a cysteine-depleted, methionine-restricted diet can improve therapeutic response to RSL3 and prolong survival in a syngeneic orthotopic murine glioma model. Finally, this CMD diet leads to profound in vivo metabolomic, proteomic and lipidomic alterations, highlighting the potential for improving the efficacy of ferroptotic therapies in glioma treatment with a non-invasive dietary modification.
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