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Cited by 282

The DOI matches its Crossref record; 104 of the 104 references it cites were found in a registry or an index.

Isocitrate dehydrogenase mutations in gliomas

Open access
Waitkus, Matthew S., Diplas, Bill H., Yan, Hai·2016·Neuro-Oncology

Abstract

Over the last decade, extraordinary progress has been made in elucidating the underlying genetic causes of gliomas. In 2008, our understanding of glioma genetics was revolutionized when mutations in isocitrate dehydrogenase 1 and 2 (IDH1/2) were identified in the vast majority of progressive gliomas and secondary glioblastomas (GBMs). IDH enzymes normally catalyze the decarboxylation of isocitrate to generate α-ketoglutarate (αKG), but recurrent mutations at Arg(132) of IDH1 and Arg(172) of IDH2 confer a neomorphic enzyme activity that catalyzes reduction of αKG into the putative oncometabolite D-2-hydroxyglutate (D2HG). D2HG inhibits αKG-dependent dioxygenases and is thought to create a cellular state permissive to malignant transformation by altering cellular epigenetics and blocking normal differentiation processes. Herein, we discuss the relevant literature on mechanistic studies of IDH1/2 mutations in gliomas, and we review the potential impact of IDH1/2 mutations on molecular classification and glioma therapy.

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Metadata

Authors
Waitkus, M. S., Diplas, B. H., & Yan, H.
Venue
Neuro-Oncology
Published
2015-07-16
Volume
18
Issue
1
Pages
16-26
ISSN
  • 1522-8517 (ISSN-L)
  • 1523-5866
OpenAlex
W1824539338
Cited by
282
References
104
FWCI
12.72
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Isocitrate dehydrogenase mutations in gliomas. https://app.cochat.ai/papers/10.1093/neuonc/nov136
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Waitkus, M. S., Diplas, B. H., & Yan, H. (2016). Isocitrate dehydrogenase mutations in gliomas. Neuro-Oncology. https://doi.org/10.1093/neuonc/nov136

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