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β-连环蛋白和E-钙黏蛋白在高级别子宫内膜癌中的表达模式与组织学亚型相关。

Beta-catenin and E-cadherin expression patterns in high-grade endometrial carcinoma are associated with histological subtype.

作者信息

Schlosshauer Peter W, Ellenson Lora Hedrick, Soslow Robert A

机构信息

Department of Pathology, Weill Medical College of Cornell University, New York, New York, USA.

出版信息

Mod Pathol. 2002 Oct;15(10):1032-7. doi: 10.1097/01.MP.0000028573.34289.04.

Abstract

Both beta-catenin and E-cadherin are epithelial cell adhesion molecules. In addition, beta-catenin is an important element of the Wnt signal transduction pathway, which has been implicated in embryogenesis and carcinogenesis, including the development of endometrial and ovarian endometrioid carcinomas. We hypothesized that the expression pattern of these two adhesion molecules may depend upon the histological subtype of endometrial carcinomas. Therefore, we compared the immunohistochemical expression of beta-catenin and E-cadherin in a set of uterine adenocarcinomas matched for high histologic grade, that is, poorly differentiated (International Federation of Gynecology and Obstetrics [FIGO] Grade III) uterine endometrioid carcinomas and uterine serous carcinomas. Seventeen FIGO Grade III endometrioid adenocarcinomas and 17 serous carcinomas were evaluated histologically and immunohistochemically with commercially available monoclonal antibodies against beta-catenin and E-cadherin. Nuclear expression of beta-catenin was observed in 8 of 17 (47%) endometrioid adenocarcinomas but in none of the serous carcinomas (P = .003). Moderate or strong E-cadherin expression was identified in 7 of 17 (41%) serous carcinomas as opposed to in only 1 of 17 (6%) endometrioid adenocarcinomas (P = .02). The majority of endometrioid adenocarcinomas showed strong beta-catenin expression coupled with weak E-cadherin expression; serous carcinomas did not exhibit a comparable trend. Our results indicate that the expression of beta-catenin and E-cadherin in high-grade endometrial cancers is strongly associated with histological subtype. These data provide further support for the distinct molecular profiles of endometrioid adenocarcinoma and serous carcinoma. Notably, differences in cell adhesion molecule expression could account for variations in patterns of tumor dissemination. The immunohistochemical staining pattern may also be useful for diagnostic purposes.

摘要

β-连环蛋白和E-钙黏蛋白均为上皮细胞黏附分子。此外,β-连环蛋白是Wnt信号转导通路的重要组成部分,该通路与胚胎发生和肿瘤发生有关,包括子宫内膜癌和卵巢子宫内膜样癌的发展。我们推测这两种黏附分子的表达模式可能取决于子宫内膜癌的组织学亚型。因此,我们比较了一组高组织学分级(即低分化,国际妇产科联盟[FIGO] III级)的子宫腺癌中β-连环蛋白和E-钙黏蛋白的免疫组化表达,这些腺癌包括子宫子宫内膜样癌和子宫浆液性癌。采用市售抗β-连环蛋白和E-钙黏蛋白的单克隆抗体,对17例FIGO III级子宫内膜样腺癌和17例浆液性癌进行了组织学和免疫组化评估。在17例子宫内膜样腺癌中有8例(47%)观察到β-连环蛋白的核表达,而浆液性癌中均未观察到(P = 0.003)。17例浆液性癌中有7例(41%)检测到中度或强E-钙黏蛋白表达,而子宫内膜样腺癌中仅1例(6%)检测到(P = 0.02)。大多数子宫内膜样腺癌表现为β-连环蛋白强表达伴E-钙黏蛋白弱表达;浆液性癌未表现出类似趋势。我们的结果表明,高级别子宫内膜癌中β-连环蛋白和E-钙黏蛋白的表达与组织学亚型密切相关。这些数据进一步支持了子宫内膜样腺癌和浆液性癌不同的分子特征。值得注意的是,细胞黏附分子表达的差异可能解释肿瘤播散模式的差异。免疫组化染色模式也可能有助于诊断。

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