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表皮生长因子受体基因扩增在脑肿瘤中的分布及其与预后的相关性

Distribution of epidermal growth factor receptor gene amplification in brain tumours and correlation to prognosis.

作者信息

Diedrich U, Lucius J, Baron E, Behnke J, Pabst B, Zoll B

机构信息

Neurologische Universitätsklinik, Göttingen, Germany.

出版信息

J Neurol. 1995 Oct;242(10):683-8. doi: 10.1007/BF00866920.

Abstract

In 75 gliomas and 31 meningiomas, mutations at the epidermal growth factor receptor (EGFR) gene locus were restricted to gliomas. The ligands of this receptor, epidermal growth factor and transforming growth factor alpha, lacked quantitative changes at their loci in gliomas and meningiomas. EGFR gene amplification occurred in astrocytomas, oligodendrogliomas, ependymomas and glioblastomas. The frequency of this mutation significantly increased with the malignancy grade and the patient's age. Especially in glioblastomas of individuals aged over 64 years, EGFR gene mutations were observed without chromosome-10-specific allele losses. This finding contradicts the hypothesis that deletion of one entire chromosome 10 regularly precedes EGFR gene amplification in primary glioblastomas of patients aged over 50 years. It was found that most individuals whose gliomas carry an EGFR gene mutation have a poor prognosis, comparable to that of glioblastoma patients even when the tumour is graded as benign.

摘要

在75例胶质瘤和31例脑膜瘤中,表皮生长因子受体(EGFR)基因位点的突变仅见于胶质瘤。该受体的配体,即表皮生长因子和转化生长因子α,在胶质瘤和脑膜瘤中的基因位点缺乏定量变化。EGFR基因扩增见于星形细胞瘤、少突胶质细胞瘤、室管膜瘤和胶质母细胞瘤。这种突变的频率随恶性程度和患者年龄显著增加。特别是在64岁以上个体的胶质母细胞瘤中,观察到EGFR基因突变而无10号染色体特异性等位基因缺失。这一发现与以下假设相矛盾:在50岁以上患者的原发性胶质母细胞瘤中,整条10号染色体的缺失通常先于EGFR基因扩增。研究发现,大多数携带EGFR基因突变的胶质瘤患者预后较差,即使肿瘤分级为良性,其预后也与胶质母细胞瘤患者相当。

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