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Illuminating the cross-talk between tumor metabolism and immunity in IDH-mutated cancers.

Abstract
Mutations in the genes encoding isocitrate dehydrogenase 1 (IDH1) and 2 (IDH2) are key drivers of diverse cancers, including gliomas and hematological malignancies. IDH mutations cause neomorphic enzymatic activity that results in the production of the oncometabolite 2-hydroxyglutarate (2-HG). In addition to 2-HG's well-known effects on tumor cells themselves, it has become increasingly clear that 2-HG directly influences the tumor microenvironment (TME). In particular, the non-cell-autonomous impact of 2-HG on the immune system likely plays a major role in shaping disease development and response to therapy. It is therefore critical to understand how IDH mutations affect the metabolism, epigenetics, and functions of tumor-infiltrating immune cells. Such knowledge may point towards new therapeutic approaches to treat IDH-mutant cancers.
AuthorsJulie Leca, Jerome Fortin, Tak W Mak
JournalCurrent opinion in biotechnology (Curr Opin Biotechnol) Vol. 68 Pg. 181-185 (04 2021) ISSN: 1879-0429 [Electronic] England
PMID33360716 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
CopyrightCopyright © 2020 Elsevier Ltd. All rights reserved.
Chemical References
  • Isocitrate Dehydrogenase
Topics
  • Cell Physiological Phenomena
  • Epigenomics
  • Glioma
  • Humans
  • Isocitrate Dehydrogenase (genetics)
  • Mutation
  • Tumor Microenvironment (genetics)

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