唾液腺多形性腺瘤和黏液表皮样癌中E-Cadherin表达的免疫组织化学分析

S. A. Moghadam, M. Pourmahdi, M. Gholamian, H. Pedram, F. A. Moghadam
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引用次数: 1

摘要

目的:e -钙粘蛋白是一种典型的钙粘蛋白,在上皮细胞粘附中起关键作用。这种蛋白质被称为增殖和侵袭的抑制因子。有限的研究调查了e -钙粘蛋白在唾液腺肿瘤中的表达。本研究旨在评估e -钙粘蛋白的表达及其在唾液腺肿瘤进展和侵袭中的可能作用。方法:采用回顾性横断面研究方法,对15例多形性腺瘤(PA)和9例粘液表皮样癌(MEC)进行免疫组织化学染色,检测E-cadherin的表达。染色程度以至少1000个肿瘤细胞中阳性染色细胞膜的百分比计算。结果:在正常唾液腺标本中,腺泡粘液细胞、浆液细胞及导管细胞周围可见强烈的膜染色。肌上皮细胞呈阴性。在PA中,形成导管、岛状细胞、细胞索和细胞片的附着细胞沿膜呈强烈染色,但间质肌上皮细胞呈阴性。MEC中,表皮样细胞和中间细胞呈强烈的膜染色。粘膜细胞也呈膜染色。经统计分析,MEC和PA的阳性细胞比例分别为82.56±11.66和67.4±7.24。差异无统计学意义(P < 0.05)。结论:E-cadherin表达不适合作为PA与MEC分化的标志。它仅与细胞表型相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunohistochemical Analysis of E-Cadherin Expression in Pleomorphic Adenoma and Mucoepidermoid Carcinoma of Salivary Glands
Objective: E-cadherin is a classic cadherin that plays a key role in epithelial cell adhesion. This protein is being referred to as the suppressor of proliferation and invasion. Limited studies have investigated E-cadherin expression in salivary gland neoplasms. This study sought to assess the expression of E-cadherin and its possible role in progression and invasion of salivary gland neoplasms. Methods: In this retrospective cross-sectional study, 15 samples of pleomorphic adenoma (PA) and 9 samples of mucoepidermoid carcinoma (MEC) were immunohistochemically stained for evaluation of E-cadherin expression. Degree of staining was calculated as the percentage of positively stained cell membranes out of a minimum of 1000 neoplastic cells. Results: In normal salivary gland specimens, intense membrane staining was observed around the acinar mucous and serous cells as well as the ductal cells. Myoepithelial cells were negative. In PA, intense staining was noted along the membrane of attached cells forming the ducts, islands, cellular cords and cellular sheets but the stromal myoepithelial cells were negative. In MEC, epidermoid and intermediate cells showed intense membrane staining. Mucous cells also showed membrane staining. After statistical analysis, the percentage of positive cells was found to be 82.56±11.66 and 67.4±7.24 in MEC and PA, respectively. This difference was not statistically significant (P>0.05). Conclusion: E-cadherin expression was not a suitable marker for differentiation of PA from MEC. It was only correlated with cell phenotype.
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