Isocitrate dehydrogenase 1and 2 gene mutation status– a critical parameter in the diagnosis and prognosis of adult gliomas

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DOI:

https://doi.org/10.3126/jpn.v11i1.28992

Keywords:

Adult glioma; IDH1/2 mutated gliomas; Immunohistochemistry; Isocitratedehydrogenase 1 and 2 genes

Abstract

Isocitrate dehydrogenase 1 and 2 mutations are known to be early events in gliomagenesis and have a definite role in tumor progression.Isocitrate dehydrogenase1/2 mutation status is considered to be one of the most powerful independent positive predictor of outcome amongst all molecular markers described in association with gliomas. The inclusion of this parameter in the 2016 update of the World Health Organization Classification of Tumors of The Central Nervous System reinforced its importance in glioma classification and prognostication. As a result, now there is enough evidence to prove that Isocitrate dehydrogenase-mutant and Isocitrate dehydrogenase- wildtypegliomas are two biologically distinct categories of gliomas with likely different pathways of tumorigenesis, different clinical outcomes, and respond differently to similar treatment strategies. Increasing knowledge aboutthe role of IDH1/2 mutation in gliomagenesis has resulted in many novel targeting strategies being developed and evaluated forusefulness in the clinical setting. This literature review aims to highlight the diagnostic and prognostic importance of Isocitrate dehydrogenase1/2 gene mutations in adult gliomas. 

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Author Biographies

Poornima Vijayan, University of Toronto, Ontario, Canada

Department of Molecular Genetics

Laila Ilias, MES Medical College, Kerala, India

Department of Pathology

Anupama Ponniah, KMCT Medical College, Kerala, India

Department of Pathology,

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Published

2021-03-20

How to Cite

Vijayan, P., Ilias, L., & Ponniah, A. (2021). Isocitrate dehydrogenase 1and 2 gene mutation status– a critical parameter in the diagnosis and prognosis of adult gliomas. Journal of Pathology of Nepal, 11(1), 1881–1885. https://doi.org/10.3126/jpn.v11i1.28992

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Section

Review Articles