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What a difference a hydroxyl makes: mutant IDH, (<i>R</i>)-2-hydroxyglutarate, and cancer

Julie-Aurore Losman, William G. Kaelin

Genes & Development · 2013 · ▲ 569 citations

Abstract

Mutations in metabolic enzymes, including isocitrate dehydrogenase 1 (IDH1) and IDH2, in cancer strongly implicate altered metabolism in tumorigenesis. IDH1 and IDH2 catalyze the interconversion of isocitrate and 2-oxoglutarate (2OG). 2OG is a TCA cycle intermediate and an essential cofactor for many enzymes, including JmjC domain-containing histone demethylases, TET 5-methylcytosine hydroxylases, and EglN prolyl-4-hydroxylases. Cancer-associated IDH mutations alter the enzymes such that they reduce 2OG to the structurally similar metabolite (R)-2-hydroxyglutarate [(R)-2HG]. Here we review what is known about the molecular mechanisms of transformation by mutant IDH and discuss their implications for the development of targeted therapies to treat IDH mutant malignancies.

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OpenAlex
DOI
10.1101/gad.217406.113
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2026-06-07 MST

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APA
Losman, J., &amp; Kaelin, W.G. (2013). What a difference a hydroxyl makes: mutant IDH, (<i>R</i>)-2-hydroxyglutarate, and cancer. <em>Genes & Development</em>. https://doi.org/10.1101/gad.217406.113
Vancouver
Losman J, Kaelin WG. What a difference a hydroxyl makes: mutant IDH, (<i>R</i>)-2-hydroxyglutarate, and cancer. Genes & Development. 2013. doi:10.1101/gad.217406.113.
BibTeX
@article{julieaurore2013Whatad, title = {What a difference a hydroxyl makes: mutant IDH, (<i>R</i>)-2-hydroxyglutarate, and cancer}, author = {Julie-Aurore Losman and William G. Kaelin}, journal = {Genes & Development}, year = {2013}, doi = {10.1101/gad.217406.113}, }

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