Agnihotri Sameer, Aldape Kenneth D, Zadeh Gelareh
Arthur and Sonia Labatt Brain Tumour Research Centre, The Hospital for Sick Children;
Neurosurg Focus. 2014 Dec;37(6):E13. doi: 10.3171/2014.9.FOCUS14505.
Diffuse gliomas and secondary glioblastomas (GBMs) that develop from low-grade gliomas are a common and incurable class of brain tumor. Mutations in the metabolic enzyme glioblastomas (IDH1) represent a distinguishing feature of low-grade gliomas and secondary GBMs. IDH1 mutations are one of the most common and earliest detectable genetic alterations in low-grade diffuse gliomas, and evidence supports this mutation as a driver of gliomagenesis. Here, the authors highlight the biological consequences of IDH1 mutations in gliomas, the clinical and therapeutic/diagnostic implications, and the molecular subtypes of these tumors. They also explore, in brief, the non-IDH1-mutated gliomas, including primary GBMs, and the molecular subtypes and drivers of these tumors. A fundamental understanding of the diversity of GBMs and lower-grade gliomas will ultimately allow for more effective treatments and predictors of survival.
弥漫性胶质瘤以及由低级胶质瘤发展而来的继发性胶质母细胞瘤(GBM)是一类常见且无法治愈的脑肿瘤。代谢酶异柠檬酸脱氢酶1(IDH1)的突变是低级胶质瘤和继发性GBM的一个显著特征。IDH1突变是低级弥漫性胶质瘤中最常见且最早可检测到的基因改变之一,有证据支持这种突变是胶质瘤发生的驱动因素。在此,作者强调了IDH1突变在胶质瘤中的生物学后果、临床及治疗/诊断意义,以及这些肿瘤的分子亚型。他们还简要探讨了非IDH1突变的胶质瘤,包括原发性GBM,以及这些肿瘤的分子亚型和驱动因素。对GBM和低级胶质瘤多样性的基本了解最终将有助于实现更有效的治疗和生存预测。