Louis D N, Rubio M P, Correa K M, Gusella J F, von Deimling A
Dept. of Pathology (Neuropathology), Massachusetts General Hospital, Boston 02114.
J Neuropathol Exp Neurol. 1993 Sep;52(5):507-15. doi: 10.1097/00005072-199309000-00009.
Brain stem gliomas are pediatric astrocytomas that histologically resemble adult supratentorial astrocytomas such as glioblastomas multiforme (GBM). Our molecular genetic studies have suggested that adult GBM can be divided into two genetic subsets: tumors with p53 tumor suppressor gene mutations and chromosome 17p loss that occur more commonly in younger patients; and tumors with epidermal growth factor receptor (EGFR) gene amplification that occur more commonly in older patients. Brain stem gliomas have not been studied since biopsies of these tumors are rare and extremely small. We investigated the molecular genetic composition of seven brain stem glioblastomas (two small biopsies, five autopsies) using polymerase chain reaction (PCR) assays for chromosomal loss, gene mutation and gene amplification. Four cases lost portions of chromosome 17p that included the p53 gene. These four cases and one additional case had mutations in the p53 gene. None of the cases showed amplification of the EGFR gene. Allelic losses of the long arm of chromosome 10 were noted in four cases. These results suggest similarities between pediatric brain stem glioblastomas and those GBM that occur in younger adult patients, and confirm the utility of PCR-based means of studying small and archival brain tumor specimens.
脑干胶质瘤是一种儿童星形细胞瘤,组织学上类似于成人幕上星形细胞瘤,如多形性胶质母细胞瘤(GBM)。我们的分子遗传学研究表明,成人GBM可分为两个基因亚群:p53肿瘤抑制基因突变和17号染色体短臂缺失的肿瘤,多见于年轻患者;表皮生长因子受体(EGFR)基因扩增的肿瘤,多见于老年患者。由于这些肿瘤的活检很少且样本极小,因此尚未对脑干胶质瘤进行研究。我们使用聚合酶链反应(PCR)检测染色体缺失、基因突变和基因扩增,对7例脑干胶质母细胞瘤(2例小活检,5例尸检)的分子遗传组成进行了研究。4例患者的17号染色体短臂部分缺失,其中包括p53基因。这4例患者和另外1例患者的p53基因发生了突变。所有病例均未显示EGFR基因扩增。4例患者出现了10号染色体长臂的等位基因缺失。这些结果表明,儿童脑干胶质母细胞瘤与年轻成年患者的GBM之间存在相似性,并证实了基于PCR研究小的存档脑肿瘤标本的实用性。