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Cancer-associated IDH mutations: biomarker and therapeutic opportunities
Abstract
The discovery of somatic mutations in the isocitrate dehydrogenase (IDH) enzymes through a genome-wide mutational analysis in glioblastoma represents a milestone event in cancer biology. The nature of the heterozygous, point mutations mapping to arginine residues involved in the substrate binding inspired several research teams to investigate their impact on the biochemical activity of these enzymes. Soon, it became clear that the mutations identified impaired the ability of IDH1 and IDH2 to catalyze the conversion of isocitrate to α-ketoglutarate (αKG), whereas conferring a gain of a novel enzymatic activity leading to the reduction of αKG to the metabolite D2-hydroxyglutarate (D-2HG). Across glioma as well as several hematologic malignancies, mutations in IDH1 and IDH2 have shown prognostic value. Several hypotheses implicating the elevated levels of D-2HG and tumorigenesis, and the therapeutic potential of targeting mutant IDH enzymes will be discussed.
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“IDH1 or IDH2 mutations lead to production of the oncometabolite D2-hydroxyglutarate (D-2HG) (Yen et al., 2010).”
From SIRT5-mediated lysine desuccinylation impacts diverse metabolic pathways (2013) · cites this paper as Yen et al., 2010
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Cites
Hanahan, D., & Weinberg, R. A. (2000) · Cell · doi:10.1016/s0092-8674(00)81683-9 · Cited by 29,219
Understanding the Warburg Effect: The Metabolic Requirements of Cell Proliferation
Vander Heiden, M. G., Cantley, L. C., & Thompson, C. B. (2009) · Science · doi:10.1126/science.1160809 · Cited by 16,197
Verhaak, R. G. W., Hoadley, K. A., Purdom, E., Wang, V., Qi, Y., Wilkerson, M. D., Miller, C. R., Ding, L., Golub, T., Mesirov, J. P., et al. (2010) · Cancer Cell · doi:10.1016/j.ccr.2009.12.020 · Cited by 7,575
An Integrated Genomic Analysis of Human Glioblastoma Multiforme
Parsons, D. W., Jones, S., Zhang, X., Lin, J. C.-H., Leary, R. J., Angenendt, P., Mankoo, P., Carter, H., Siu, I.-M., Gallia, G. L., et al. (2008) · Science · doi:10.1126/science.1164382 · Cited by 5,857
IDH1 and IDH2 Mutations in Gliomas
Yan, H., Parsons, D. W., Jin, G., McLendon, R., Rasheed, B. A., Yuan, W., Kos, I., Batinic-Haberle, I., Jones, S., Riggins, G. J., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0808710 · Cited by 5,847
The fundamental role of epigenetic events in cancer
Jones, P. A., & Baylin, S. B. (2002) · Nature Reviews Genetics · doi:10.1038/nrg816 · Cited by 5,648
Cancer-associated IDH1 mutations produce 2-hydroxyglutarate
Dang, L., White, D. W., Gross, S., Bennett, B. D., Bittinger, M. A., Driggers, E. M., Fantin, V. R., Jang, H. G., Jin, S., Keenan, M. C., et al. (2009) · Nature · doi:10.1038/nature08617 · Cited by 4,154
Self-citationThe Consensus Coding Sequences of Human Breast and Colorectal Cancers
Sjöblom, T., Jones, S., Wood, L. D., Parsons, D. W., Lin, J., Barber, T. D., Mandelker, D. L., Leary, R. J., Ptak, J., Silliman, N., et al. (2006) · Science · doi:10.1126/science.1133427 · Cited by 3,161
Tumor cell metabolism: cancer's Achilles' heel
Kroemer, G., & Pouyssegur, J. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.05.005 · Cited by 2,337
Identification of a CpG Island Methylator Phenotype that Defines a Distinct Subgroup of Glioma
Noushmehr, H., Weisenberger, D. J., Diefes, K., Phillips, H. S., Pujara, K., Berman, B. P., Pan, F., Pelloski, C. E., Sulman, E. P., Bhat, K. P., et al. (2010) · Cancer Cell · doi:10.1016/j.ccr.2010.03.017 · Cited by 2,337
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Ocampo-Navia, M. I., Marín-Navas, F., Agudelo-Arrieta, M., Taub-Krivoy, A., & Lee, O. H. F. (2025) · Interdisciplinary Neurosurgery · doi:10.1016/j.inat.2025.102062 · Cited by 9
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Shi, Z., Zhou, H., Pan, B., Lu, L., Kang, Y., Liu, L., Wei, Z., & Feng, S. (2017) · Oncotarget · doi:10.18632/oncotarget.16700 · Cited by 9
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Alentorn, A., Labussière, M., Sanson, M., Delattre, J., Hoang‐Xuan, K., & Idbaïh, A. (2012) · La Presse Médicale · doi:10.1016/j.lpm.2012.05.013 · Cited by 8
Yao, K., Liu, H., Liu, P., Liu, W., Yang, J., Wei, Q., Cao, P., & Lai, Y. (2020) · Computational Biology and Chemistry · doi:10.1016/j.compbiolchem.2020.107261 · Cited by 7
Modrzejewska, M., Gawroński, M., & Gackowski, D. (2021) · Analytical Biochemistry · doi:10.1016/j.ab.2021.114129 · Cited by 7
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Yao, K., Liu, P., Liu, H., Wei, Q., Yang, J., Cao, P., & Lai, Y. (2019) · Journal of Molecular Structure · doi:10.1016/j.molstruc.2019.03.092 · Cited by 8
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Duzan, A., Reinken, D. N., McGomery, T. L., Ferencz, N. M., Plummer, J. M., & Basti, M. M. (2023) · Journal of Chinese Integrative Medicine · doi:10.1016/j.joim.2023.01.005 · Cited by 7
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Tuna, M., & Christopher, I. L. (2012) · InTech eBooks · doi:10.5772/48701 · Cited by 8
Wan, S., Wu, Y., Zhou, X., Chen, Y., An, J., Yu, X., Zhang, H., Yang, H., & Xing, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124471 · Cited by 7
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Velculescu, V. E., & Diaz, L. A. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3003001 · Cited by 6
Du, X., Wan, S., Chen, Y., Qü, P., Huang, X., Yu, X., Yang, H., Zhang, Y., & Xing, J. (2014) · Annals of Surgical Oncology · doi:10.1245/s10434-014-3876-2 · Cited by 6
Bories, P.-N., Nakib, S., Cynober, L., Alary, A., Coudé, M.-M., Chevillon, F., Tamburini, J., Birsen, R., Kosmider, O., & Bouscary, D. (2018) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm-2018-0427 · Cited by 5
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Ho, C., & Kluk, M. (2016) · Surgical pathology clinics · doi:10.1016/j.path.2016.04.011 · Cited by 4
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Classe, M. (2017) · theses.fr (ABES) · doi:10.70675/e9d57129zf812z42c4zb161zf119c8d906c3
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BindingDB Entry 50013577: Discovery and Optimization of 2
BindingDB (2022) · UC San Diego · doi:10.7270/q2ff3x3s
BindingDB (2013) · UC San Diego · doi:10.7270/q2x92cf7
Robinson, G. L. (2012) · Leicester Research Archive (University of Leicester)
Metadata
- Authors
- Yen, K. E., Bittinger, M. A., Su, S. M., & Fantin, V. R.
- Affiliations
- Agios Pharmaceuticals (United States) (US)
- Corresponding author
- Fantin, V R
- ORCID
- Venue
- Oncogene
- Published
- 2010-10-25
- Volume
- 29
- Issue
- 49
- Pages
- 6409-6417
- ISSN
- 0950-9232 (ISSN-L)
- 1476-5594
- OpenAlex
- W2002134084
- Cited by
- 296
- References
- 63
- Citations by year
- 2026: 3 · 2025: 8 · 2024: 11 · 2023: 17 · 2022: 16 · 2021: 23 · 2020: 21 · 2019: 21 · 2018: 22 · 2017: 23 · 2016: 16 · 2015: 16 · 2014: 18 · 2013: 29 · 2012: 27
- FWCI
- 2.93
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Oncogene (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Glioma Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer, Hypoxia, and Metabolism
- Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
- Keywords
- IDH mutation, IDH1, IDH2, glioblastoma, glioma, hematologic malignancies, gain-of-function mutations, alpha-ketoglutarate, prognostic factors, carcinogenesis
- MeSH terms
- Glioma, Glutarates, Humans, Isocitrate Dehydrogenase, Oncogenes, Biomarkers, Tumor, Central Nervous System Neoplasms, Point Mutation, Hematologic Neoplasms
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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