Eppenberger U, Mueller H
Department of Gynecology, Kantonsspital, Basel, Switzerland.
J Neurooncol. 1994;22(3):249-54. doi: 10.1007/BF01052929.
The understanding of the signal transduction cascade involving growth factors and their receptors is one major key for diagnostic and therapeutic improvements in human neoplasms. Using receptor autoradiography, an inverse relationship for the incidence of somatostatin receptors (SSR) and epidermal growth factor receptors (EGFR) was found in gliomas [1]. In the majority of low grade gliomas, SSR were present but EGFR were absent. In contrast, EGFR were present in most glioblastomas, but no SSR were detected. Recently, the amplification of the EGFR gene and its overexpression was demonstrated to be associated with the development of glioblastomas. Several independent reports revealed that 40-50% of tumors show amplified EGFR [2-4]. The frequency of EGFR amplification was directly associated with tumor malignancy. In addition, amplified EGFR levels indicate a bad prognosis and shorter overall survival [5]. Recent analysis of the EGFR gene in tumors has shown that regions of this gene frequently undergo alteration. Hence, not only amplification but also mutation may be the cause of the increased malignancy in EGFR overexpressing cells [6].
对涉及生长因子及其受体的信号转导级联的理解是人类肿瘤诊断和治疗改善的一个主要关键。利用受体放射自显影术,在胶质瘤中发现生长抑素受体(SSR)和表皮生长因子受体(EGFR)的发生率呈负相关[1]。在大多数低级别胶质瘤中,存在SSR但不存在EGFR。相反,大多数胶质母细胞瘤中存在EGFR,但未检测到SSR。最近,EGFR基因的扩增及其过表达被证明与胶质母细胞瘤的发生有关。几项独立报告显示,40-50%的肿瘤显示EGFR扩增[2-4]。EGFR扩增的频率与肿瘤恶性程度直接相关。此外,扩增的EGFR水平表明预后不良和总生存期较短[5]。最近对肿瘤中EGFR基因的分析表明,该基因区域经常发生改变。因此,不仅扩增而且突变可能是EGFR过表达细胞恶性程度增加的原因[6]。