| Literature DB >> 25670081 |
Lingtao Jin1, Dan Li1, Gina N Alesi1, Jun Fan1, Hee-Bum Kang1, Zhou Lu2, Titus J Boggon3, Peng Jin4, Hong Yi5, Elizabeth R Wright6, Duc Duong7, Nicholas T Seyfried7, Robert Egnatchik8, Ralph J DeBerardinis8, Kelly R Magliocca9, Chuan He2, Martha L Arellano1, Hanna J Khoury1, Dong M Shin1, Fadlo R Khuri1, Sumin Kang10.
Abstract
How mitochondrial glutaminolysis contributes to redox homeostasis in cancer cells remains unclear. Here we report that the mitochondrial enzyme glutamate dehydrogenase 1 (GDH1) is commonly upregulated in human cancers. GDH1 is important for redox homeostasis in cancer cells by controlling the intracellular levels of its product alpha-ketoglutarate and subsequent metabolite fumarate. Mechanistically, fumarate binds to and activates a reactive oxygen species scavenging enzyme glutathione peroxidase 1. Targeting GDH1 by shRNA or a small molecule inhibitor R162 resulted in imbalanced redox homeostasis, leading to attenuated cancer cell proliferation and tumor growth.Entities:
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Year: 2015 PMID: 25670081 PMCID: PMC4325424 DOI: 10.1016/j.ccell.2014.12.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743