Campbell Family Institute for Breast Cancer Research at Princess Margaret Hospital, University Health Network, Toronto, ON, Canada.
Blood. 2012 Feb 23;119(8):1901-3. doi: 10.1182/blood-2011-11-391748. Epub 2012 Jan 3.
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.
IDH1 和 IDH2 中的突变发生在大多数 2 级和 3 级胶质瘤、继发性胶质母细胞瘤和一部分急性髓系白血病中,但未在其他肿瘤类型中检测到。这些突变发生在特定的精氨酸残基上,导致获得一种新的酶活性,将 2-氧戊二酸转化为 D-2-羟基戊二酸。本研究报告了一组淋巴瘤的 IDH1 和 IDH2 基因分型结果,其中包括一大组外周 T 细胞淋巴瘤。IDH2 突变约见于 20%的血管免疫母细胞性 T 细胞淋巴瘤(AITL),但不发生于其他外周 T 细胞淋巴瘤实体。在一组独立的 AITL 患者中,该结果得到了证实,其中 IDH2 突变率约为 45%。这是继 TET2 之后在 AITL 中发现的第二个常见遗传病变,增加了 IDH1 和 IDH2 突变可能发挥作用的肿瘤疾病数量。