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人神经系统肿瘤中表皮生长因子受体表达与生长分数

Epidermal growth factor receptor expression and growth fraction in human tumours of the nervous system.

作者信息

Reifenberger G, Prior R, Deckert M, Wechsler W

机构信息

Department of Neuropathology, University of Düsseldorf, Federal Republic of Germany.

出版信息

Virchows Arch A Pathol Anat Histopathol. 1989;414(2):147-55. doi: 10.1007/BF00718594.

Abstract

100 tumours of the human nervous system were investigated by means of immunohistochemistry in order to determine the expression of epidermal growth factor receptor (EGFr) and the proliferative activity as evaluated by demonstration of the proliferation-associated Ki-67 antigen. Epidermal growth factyr receptor immunoreactivity was present in 79% (23/29) of the high-grade malignant gliomas examined but in only 9% (2/22) of the low-grade gliomas. Besides the gliomas, EGFr-expression was detectable in smaller amounts in most (13/15) meningiomas, in one anaplastic neurinoma and in individual tumour cells of one medulloblastoma. In addition, EGFr-expression was found in 50% (6/12) of metastatic carcinomas. Seven of eight medulloblastomas, two cerebral primitive neuroectodermal tumours (PNETs), three benign neurinomas, one ganglioneuroma, one metastatic intracerebral malignant melanoma, three spinal plasmacytomas and one immunocytoma showed no detectable EGFr-expression. Our results indicate that (1) the expression of EGFr in human tumours of the nervous system depends on the histological tumour type and (2) in the glioma group is related to the grade of malignancy. A close correlation between EGFr-expression and proliferative activity as evaluated by Ki-67 staining could not, however, be established.

摘要

采用免疫组织化学方法对100例人类神经系统肿瘤进行研究,以确定表皮生长因子受体(EGFr)的表达情况以及通过增殖相关的Ki-67抗原检测评估的增殖活性。在检查的高级别恶性胶质瘤中,79%(23/29)存在表皮生长因子受体免疫反应性,但在低级别胶质瘤中仅为9%(2/22)。除胶质瘤外,大多数(13/15)脑膜瘤、1例间变性神经鞘瘤和1例髓母细胞瘤的个别肿瘤细胞中可检测到少量的EGFr表达。此外,在50%(6/12)的转移性癌中发现有EGFr表达。8例髓母细胞瘤中的7例、2例脑原始神经外胚层肿瘤(PNETs)、3例良性神经鞘瘤、1例神经节细胞瘤、1例脑内转移性恶性黑色素瘤、3例脊髓浆细胞瘤和1例免疫细胞瘤均未检测到EGFr表达。我们的结果表明:(1)人类神经系统肿瘤中EGFr的表达取决于肿瘤的组织学类型;(2)在胶质瘤组中与恶性程度相关。然而,通过Ki-67染色评估,EGFr表达与增殖活性之间未发现密切相关性。

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