Tauchi K, Hori S, Itoh H, Osamura R Y, Tokuda Y, Tajima T
Department of Pathology, Tokai University School of Medicine, Isehara, Japan.
Virchows Arch A Pathol Anat Histopathol. 1989;416(1):65-73. doi: 10.1007/BF01606471.
It is a matter of debate whether the amplification of c-erbB-2 oncogene or production of the oncoprotein in breast cancers correlate with the presence of lymph node metastasis and with a poor prognosis. This study was aimed at elucidating the immunohistochemical localization of oncogene products which are related to cell growth, c-erbB-2 product, epidermal growth factor receptor (EGFR), c-myc protein and estrogen receptor (ER), in benign and malignant lesions of the breast. Fresh frozen sections of 25 breast cancers and 11 fibroadenomas from Japanese women were studied by indirect immunoperoxidase method with proper fixation. C-erbB-2 product and EGFR were localized on the cell membrane whereas c-myc protein and ER were observed in the nuclei. Immunohistochemical expression of oncogene products and ER were not only observed in the mammary carcinomas but also in the fibroadenomas. However immunoreactivities of EGFR and ER were more frequently seen in the fibroadenomas (p less than 0.05). In breast cancers, the incidence of immunoreactivity for c-erbB-2 was higher in the cases with lymph node metastasis than cases without nodal metastasis (p less than 0.05) and there was reciprocal correlation between the expressions of EGFR and ER (p less than 0.05). Regarding the size of the primary tumour, there was no statistically significant correlation with the expressions of c-erbB-2, EGFR, c-myc or ER. Histological grade correlated only with the expression of ER (p less than 0.05).
乳腺癌中c-erbB-2癌基因的扩增或癌蛋白的产生是否与淋巴结转移及预后不良相关,这是一个存在争议的问题。本研究旨在阐明与细胞生长相关的癌基因产物、c-erbB-2产物、表皮生长因子受体(EGFR)、c-myc蛋白和雌激素受体(ER)在乳腺良恶性病变中的免疫组化定位。采用间接免疫过氧化物酶法并进行适当固定,对25例日本女性乳腺癌和11例纤维腺瘤的新鲜冰冻切片进行了研究。c-erbB-2产物和EGFR定位于细胞膜,而c-myc蛋白和ER在细胞核中观察到。癌基因产物和ER的免疫组化表达不仅在乳腺癌中可见,在纤维腺瘤中也可见。然而,EGFR和ER的免疫反应性在纤维腺瘤中更常见(p<0.05)。在乳腺癌中,有淋巴结转移的病例中c-erbB-2免疫反应性的发生率高于无淋巴结转移的病例(p<0.05),且EGFR和ER的表达之间呈负相关(p<0.05)。关于原发肿瘤的大小,与c-erbB-2、EGFR、c-myc或ER的表达无统计学显著相关性。组织学分级仅与ER的表达相关(p<0.05)。