首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Differential loss of E-cadherin expression in infiltrating ductal and lobular breast carcinomas.
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Differential loss of E-cadherin expression in infiltrating ductal and lobular breast carcinomas.

机译:浸润性导管和小叶乳腺癌中E-钙黏着蛋白表达的差异丢失。

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摘要

The epithelial-specific cell-cell adhesion molecule E-cadherin was analyzed immunohistochemically on tissue sections of 89 human primary infiltrating breast carcinomas, using monoclonal antibodies 6F9 (for cryostat sections) and 5H9 (for cryostat and paraffin sections). The tumors included 41 well and moderately differentiated infiltrating ductal carcinomas (IDCs) most of which (78%) showed strong linear staining at the cell borders at a level, as high as luminal cells of normal mammary glands. The 26 poorly differentiated, more highly malignant IDCs examined also were all positive for E-cadherin, although a higher proportion of them (54%) showed reduced staining, which was heterogeneous and dotted over the cell borders. In contrast, 19 of 22 infiltrating lobular carcinomas (ILCs), which were either of the dispersed (classical), solid, or the mixed type, did not express E-cadherin, whereas three cases showed weak staining. In situ lesions of ILCs and pure lobular carcinoma in situ (four cases) were all E-cadherin negative, whereas intraductal carcinomas (11 cases) exhibited mostly strong staining. The results were confirmed by Western blotting. The data indicate that loss of E-cadherin expression is an early event in the formation of the lobular type of breast carcinomas. The absence of E-cadherin signifies a partial loss of epithelial differentiation and may account for the extended spread of lobular carcinoma in situ and the peculiar diffuse invasion mode of ILC. The generation of dedifferentiated IDCs can only in part be correlated with reduced expression of the intercellular adhesion molecule E-cadherin. Other factors are obviously also involved during invasion of this carcinoma type.
机译:使用单克隆抗体6F9(用于低温恒温器切片)和5H9(用于低温恒温器和石蜡切片)在89例人类原发性浸润性乳腺癌的组织切片上免疫组织化学分析了上皮特异性细胞-细胞粘附分子E-cadherin。肿瘤包括41例分化良好的中度浸润性导管癌(IDC),其中大多数(78%)在细胞边界处表现出强烈的线性染色,水平与正常乳腺的腔细胞一样高。检查的26个分化差,恶性程度更高的IDC都对E-钙粘着蛋白均为阳性,尽管它们中较高的比例(54%)显示出减少的染色,这是异质的,并散布在细胞边界上。相比之下,在22种浸润性小叶癌(ILC)中,有19种不表达E-钙黏着蛋白,无论是分散型(经典型),实体型还是混合型,均不表达E-钙粘着蛋白。 ILCs的原位病变和纯小叶原位癌(4例)均为E-cadherin阴性,而导管内癌(11例)则表现为强染色。通过蛋白质印迹证实了结果。数据表明,E-钙粘蛋白表达的丧失是小叶型乳腺癌形成的早期事件。 E-钙粘着蛋白的缺乏表明上皮分化的部分丧失,并可能解释了小叶癌的原位扩展扩散和ILC特有的弥漫性浸润模式。去分化的IDC的产生仅部分与细胞间粘附分子E-钙粘着蛋白的表达降低有关。显然,在这种癌症的侵袭过程中还涉及其他因素。

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