| Literature DB >> 29056515 |
Lucia Salamanca-Cardona1, Hardik Shah2, Alex J Poot1, Fabian M Correa1, Valentina Di Gialleonardo1, Hui Lui2, Vesselin Z Miloushev1, Kristin L Granlund1, Sui S Tee1, Justin R Cross2, Craig B Thompson3, Kayvan R Keshari4.
Abstract
The oncometabolite 2-hydroxyglutarate (2-HG) is a signature biomarker in various cancers, where it accumulates as a result of mutations in isocitrate dehydrogenase (IDH). The metabolic source of 2-HG, in a wide variety of cancers, dictates both its generation and also potential therapeutic strategies, but this remains difficult to access in vivo. Here, utilizing patient-derived chondrosarcoma cells harboring endogenous mutations in IDH1 and IDH2, we report that 2-HG can be rapidly generated from glutamine in vitro. Then, using hyperpolarized magnetic resonance imaging (HP-MRI), we demonstrate that in vivo HP [1-13C] glutamine can be used to non-invasively measure glutamine-derived HP 2-HG production. This can be readily modulated utilizing a selective IDH1 inhibitor, opening the door to targeting glutamine-derived 2-HG therapeutically. Rapid rates of HP 2-HG generation in vivo further demonstrate that, in a context-dependent manner, glutamine can be a primary carbon source for 2-HG production in mutant IDH tumors.Entities:
Keywords: 2-hydroxyglutarate; glutamine; hyperpolarized imaging; mutant isocitrate dehydrogenase
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Year: 2017 PMID: 29056515 PMCID: PMC5718944 DOI: 10.1016/j.cmet.2017.10.001
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 31.373