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. 2018 Aug;73(2):299-305.
doi: 10.1111/his.13525. Epub 2018 May 31.

Frequent loss of claudin-4 expression in dedifferentiated and undifferentiated endometrial carcinomas

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Frequent loss of claudin-4 expression in dedifferentiated and undifferentiated endometrial carcinomas

Basile Tessier-Cloutier et al. Histopathology. 2018 Aug.

Abstract

Aims: Dedifferentiated endometrial carcinomas (DDECs)/undifferentiated endometrial carcinomas (UECs) are aggressive endometrial cancers with frequent genomic inactivation of core components of switch/sucrose non-fermentable (SWI/SNF) complex proteins. Claudin-4, an epithelial intercellular tight junction protein, was recently found to be expressed in SWI/SNF-deficient undifferentiated carcinomas but not in SWI/SNF-deficient sarcomas. The aim of this study was to examine claudin-4 expression in UECs/DDECs and other high-grade uterine carcinomas.

Methods and results: We examined claudin-4 expression by immunohistochemistry (clone 3E2C1) on tissue microarrays that contained 44 UECs/DDECs (24 SWI/SNF-deficient), 50 carcinosarcomas, 164 grade 3 endometrioid carcinomas, 57 serous carcinomas, and 20 clear cell carcinomas. Tumours with <5% claudin-4 expression were considered to be negative. Nearly all SWI/SNF-deficient, and most SWI/SNF-proficient, UECs/DDECs showed a complete absence of claudin-4 expression in the undifferentiated component, whereas the differentiated component in DDECs showed consistent and diffuse claudin-4 expression. Only one SWI/SNF-deficient DDEC showed focal expression of claudin-4 in the undifferentiated component, as compared with diffuse expression in the corresponding differentiated component. Claudin-4 expression was consistently absent in the sarcomatous component of carcinosarcoma, and it was absent in 24% of grade 3 endometrioid carcinomas and serous carcinomas.

Conclusion: Claudin-4 expression can be absent or very focal in a subset of high-grade endometrial carcinomas, and is almost always absent in the undifferentiated components of SWI/SNF-deficient UECs/DDECs, despite the apparent epithelial origin in the case of DDECs. Therefore, claudin-4 expression cannot be used to infer mesenchymal or epithelial tumour origin in the endometrium. The consistent loss or down-regulation of claudin-4, a tight junction protein, in SWI/SNF-deficient UECs/DDECs further supports the undifferentiated nature of these tumours.

Keywords: SWI/SNF proteins; claudin-4; endometrial cancer; endometrioid adenocarcinoma; undifferentiated carcinoma; uterine sarcomas.

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Conflict of interest statement

Disclosure: The study authors have no conflicts of interest to declare.

Figures

Figure 1:
Figure 1:
Claudin-4 immunohistochemistry DDEC/UEC. A-D) Two cases of SWI/SNF-deficient DDEC showing absent claudin-4 expression in undifferentiated component and diffuse claudin-4 expression in the differentiated component. E-F) A case of SWI/SNF-deficient UEC showing focal expression of claudin-4.
Figure 2:
Figure 2:
Representative examples of claudin-4 expression in a carcinosarcoma (A-B) and a leiomyosarcoma (C-D).

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