Department of Pathology, East-West Neo Medical Centre, School of Medicine, Kyung Hee University, 149 Sangil-Dong, Gangdong-Gu, Seoul 134-727, Korea.
Histopathology. 2010 May;56(6):708-19. doi: 10.1111/j.1365-2559.2010.03534.x.
Previous investigations have indicated that stromal CD10 expression, and altered levels of both E-cadherin and beta-catenin, are associated with the biological aggressiveness of human carcinoma. The aim was to evaluate stromal CD10 expression and the association of stromal CD10 with E-cadherin and beta-catenin in breast carcinoma.
The expression of CD10, E-cadherin and beta-catenin was immunohistochemically analysed in tissue microarrays containing 104 cases of invasive ductal carcinoma (IDC) and 10 cases of ductal carcinoma in situ (DCIS). Stromal CD10 was detected in 49.5% (50/101) of the IDC. No immunoreactivity was identified in the stromal cells of normal breast, DCIS or intraductal components of IDC. Accumulation of the cytoplasmic beta-catenin was found in 87.0% (87/100) of the IDC. Stromal CD10 expression in IDC was significantly correlated with tumour size (P = 0.027), stage (P < 0.001) and histological grade (P = 0.006), the presence of nodal (P = 0.048) and distant (P = 0.015) metastases, oestrogen receptor-negative status (P = 0.016), cytoplasmic beta-catenin accumulation (P = 0.031) and lower overall survival rate (P = 0.041).
Stromal CD10 expression in IDC may constitute an important prognostic marker. Stromal CD10 expression with associated aggressive features might be related to aberrant beta-catenin expression.
先前的研究表明,基质 CD10 的表达以及 E-钙黏蛋白和β-连环蛋白水平的改变与人类癌的生物学侵袭性有关。本研究旨在评估乳腺癌中基质 CD10 的表达及其与 E-钙黏蛋白和β-连环蛋白的相关性。
使用组织微阵列对包含 104 例浸润性导管癌(IDC)和 10 例导管原位癌(DCIS)的组织进行 CD10、E-钙黏蛋白和β-连环蛋白的免疫组织化学分析。在 101 例 IDC 中,有 49.5%(50/101)检测到基质 CD10 的表达。正常乳腺、DCIS 或 IDC 的导管内成分的基质细胞均无免疫反应性。在 87.0%(87/100)的 IDC 中发现细胞质β-连环蛋白的积累。IDC 中的基质 CD10 表达与肿瘤大小(P = 0.027)、分期(P < 0.001)和组织学分级(P = 0.006)、淋巴结(P = 0.048)和远处(P = 0.015)转移的存在、雌激素受体阴性状态(P = 0.016)、细胞质β-连环蛋白的积累(P = 0.031)和总体生存率降低(P = 0.041)显著相关。
IDC 中的基质 CD10 表达可能是一个重要的预后标志物。与侵袭性特征相关的基质 CD10 表达可能与异常的β-连环蛋白表达有关。