In Vivo Imaging of Glutamine Metabolism to the Oncometabolite 2-Hydroxyglutarate in IDH1/2 Mutant Tumors

被引:86
作者
Salamanca-Cardona, Lucia [1 ,2 ]
Shah, Hardik [3 ]
Poot, Alex J. [1 ,2 ]
Correa, Fabian M. [1 ,2 ]
Di Gialleonardo, Valentina [1 ,2 ]
Lui, Hui [3 ]
Miloushev, Vesselin Z. [1 ,2 ]
Granlund, Kristin L. [1 ,2 ]
Tee, Sui S. [1 ,2 ]
Cross, Justin R. [3 ]
Thompson, Craig B. [5 ]
Keshari, Kayvan R. [1 ,2 ,4 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiol, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Mol Pharmacol Program, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Donald B & Catherine C Marron Canc Metab Ctr, New York, NY 10065 USA
[4] Weill Cornell Med Coll, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, Canc Biol & Genet Program, New York, NY 10065 USA
关键词
MAGNETIC-RESONANCE-SPECTROSCOPY; DYNAMIC NUCLEAR-POLARIZATION; ISOCITRATE DEHYDROGENASE 1; ACUTE MYELOID-LEUKEMIA; CANCER METABOLISM; GLIOMA-CELLS; MUTATIONS; INHIBITOR; THERAPY; SUPPLEMENTATION;
D O I
10.1016/j.cmet.2017.10.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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-C-13] 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.
引用
收藏
页码:830 / +
页数:15
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