Department of Neuropathology, Heinrich-Heine-University, Duesseldorf, Germany.
Acta Neuropathol. 2010 Nov;120(5):567-84. doi: 10.1007/s00401-010-0736-4. Epub 2010 Aug 17.
Modern neuropathology serves a key function in the multidisciplinary management of brain tumor patients. Owing to the recent advancements in molecular neurooncology, the neuropathological assessment of brain tumors is no longer restricted to provide information on a tumor's histological type and malignancy grade, but may be complemented by a growing number of molecular tests for clinically relevant tissue-based biomarkers. This article provides an overview and critical appraisal of the types of genetic and epigenetic aberrations that have gained significance in the molecular diagnostics of gliomas, namely deletions of chromosome arms 1p and 19q, promoter hypermethylation of the O6-methylguanine-methyl-transferase (MGMT) gene, and the mutation status of the IDH1 and IDH2 genes. In addition, the frequent oncogenic aberration of BRAF in pilocytic astrocytomas may serve as a novel diagnostic marker and therapeutic target. Finally, this review will summarize recent mechanistic insights into the molecular alterations underlying treatment resistance in malignant gliomas and outline the potential of genome-wide profiling approaches for increasing our repertoire of clinically useful glioma markers.
现代神经病理学在脑肿瘤患者的多学科管理中起着关键作用。由于分子神经肿瘤学的最新进展,脑肿瘤的神经病理学评估不再仅限于提供肿瘤组织学类型和恶性程度的信息,还可以通过越来越多的分子测试来补充,以检测临床相关的基于组织的生物标志物。本文概述并批判性地评价了在胶质瘤的分子诊断中具有重要意义的遗传和表观遗传异常类型,即染色体臂 1p 和 19q 的缺失、O6-甲基鸟嘌呤-DNA-甲基转移酶 (MGMT) 基因启动子的高甲基化,以及 IDH1 和 IDH2 基因突变状态。此外,毛细胞星形细胞瘤中 BRAF 的频繁致癌异常可作为一种新的诊断标志物和治疗靶点。最后,本文综述了恶性胶质瘤治疗耐药性背后分子改变的最新机制见解,并概述了全基因组分析方法在增加临床有用的胶质瘤标志物方面的潜力。