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卵巢子宫内膜样癌和卵巢浆液性癌分子差异的特征。

Characterization of the molecular differences between ovarian endometrioid carcinoma and ovarian serous carcinoma.

机构信息

Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CHUM)/Institut du Cancer de Montréal, Montréal, Canada.

出版信息

J Pathol. 2010 Feb;220(3):392-400. doi: 10.1002/path.2659.

Abstract

The histopathological diagnosis of high-grade endometrioid and serous carcinoma of the ovary is poorly reproducible under the current morphology based classification system, especially for anaplastic, high-grade tumours. The transcription factor Wilms' tumour-1 (WT1) is differentially expressed among the gynaecological epithelia from which epithelial ovarian cancers (EOCs) are believed to originate. In EOCs, WT1 protein is observed in the majority of serous carcinomas and in up to 30% of endometrioid carcinomas. It is unclear whether the latter is a reflection of the actual incidence of WT1 protein expression in endometrioid carcinomas, or whether a significant number of high-grade serous carcinomas have been misclassified as endometrioid carcinoma. Several genetic aberrations are reported to occur in EOCs. These include mutation of the TP53 gene, aberrant activation of beta-catenin signalling and loss of PTEN protein expression, among others. It is unclear whether these aberrations are histotype-specific. The aim of this study was to better define the molecular characteristics of serous and endometrioid carcinomas in an attempt to address the problems with the current histopathological classification methods. Gene expression profiles were analysed to identify reproducible gene expression phenotypes for endometrioid and serous carcinomas. Tissue microarrays (TMA) were used to assess the incidence of TP53, beta-catenin and PTEN aberrations in order to correlate their occurrence with WT1 as an immunohistochemistry based biomarker of serous histotype. It was found that nuclear WT1 protein expression can identify misclassified high-grade endometrioid carcinomas and these tumours should be reassigned to serous histotype. Although low-grade endometrioid carcinomas rarely progress to high-grade carcinomas, a combined WT1-negative, TP53-positive immunophenotype may identify an uncommon high-grade subtype of ovarian endometrioid carcinoma. GEO database: array data accession number GSE6008.

摘要

卵巢高级别子宫内膜样和浆液性癌的组织病理学诊断在当前基于形态学的分类系统下重复性较差,尤其是对于间变性、高级别肿瘤。转录因子 Wilms 瘤-1(WT1)在妇科上皮细胞中表达不同,而上皮性卵巢癌(EOC)被认为起源于这些上皮细胞。在 EOC 中,WT1 蛋白在大多数浆液性癌和多达 30%的子宫内膜样癌中观察到。目前尚不清楚后者是否反映了子宫内膜样癌中 WT1 蛋白表达的实际发生率,还是大量高级别浆液性癌被错误分类为子宫内膜样癌。据报道,EOC 中存在几种遗传异常。其中包括 TP53 基因突变、β-连环蛋白信号异常激活和 PTEN 蛋白表达缺失等。目前尚不清楚这些异常是否与组织类型有关。本研究旨在更好地定义浆液性和子宫内膜样癌的分子特征,试图解决当前组织病理学分类方法存在的问题。通过分析基因表达谱来鉴定子宫内膜样癌和浆液性癌的可重复基因表达表型。使用组织微阵列(TMA)评估 TP53、β-连环蛋白和 PTEN 异常的发生率,以将其与作为浆液性组织类型免疫组织化学生物标志物的 WT1 相关联。结果发现,核 WT1 蛋白表达可鉴定出分类错误的高级别子宫内膜样癌,这些肿瘤应重新分配为浆液性组织类型。虽然低级别子宫内膜样癌很少进展为高级别癌,但 WT1 阴性、TP53 阳性的免疫表型可能会识别出卵巢子宫内膜样癌中一种罕见的高级别亚型。GEO 数据库:阵列数据访问号 GSE6008。

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