IDH2 mutations are frequent in angioimmunoblastic T-cell lymphoma.


Autoria(s): Cairns R.A.; Iqbal J.; Lemonnier F.; Kucuk C.; de Leval L.; Jais J.P.; Parrens M.; Martin A.; Xerri L.; Brousset P.; Chan L.C.; Chan W.C.; Gaulard P.; Mak T.W.
Data(s)

2012

Resumo

Mutations in isocitrate dehydrogenase 1 (IDH1) and isocitrate dehydrogenase 2 (IDH2) occur in most grade 2 and 3 gliomas, secondary glioblastomas, and a subset of acute myelogenous leukemias but have not been detected in other tumor types. The mutations occur at specific arginine residues and result in the acquisition of a novel enzymatic activity that converts 2-oxoglutarate to D-2-hydroxyglutarate. This study reports IDH1 and IDH2 genotyping results from a set of lymphomas, which included a large set of peripheral T-cell lymphomas. IDH2 mutations were identified in approximately 20% of angioimmunoblastic T-cell lymphomas (AITLs), but not in other peripheral T-cell lymphoma entities. These results were confirmed in an independent set of AITL patients, where the IDH2 mutation rate was approximately 45%. This is the second common genetic lesion identified in AITL after TET2 and extends the number of neoplastic diseases where IDH1 and IDH2 mutations may play a role.

Identificador

https://serval.unil.ch/?id=serval:BIB_DBE8A1B7A108

isbn:1528-0020 (Electronic)

pmid:22215888

doi:10.1182/blood-2011-11-391748

isiid:000300713800019

Idioma(s)

en

Fonte

Blood, vol. 119, no. 8, pp. 1901-1903

Palavras-Chave #Aged; Female; Gene Frequency; Genotype; Humans; Immunoblastic Lymphadenopathy/enzymology; Immunoblastic Lymphadenopathy/genetics; Isocitrate Dehydrogenase/genetics; Kaplan-Meier Estimate; Lymphoma, T-Cell/enzymology; Lymphoma, T-Cell/genetics; Lymphoma, T-Cell, Peripheral/enzymology; Lymphoma, T-Cell, Peripheral/genetics; Male; Mutation; Mutation Rate; Prognosis
Tipo

info:eu-repo/semantics/article

article