[The morphological and immunohiochemical features of foci of adenomyosis: in its concurrence with endometrial adenocarcinoma].

Arkhiv patologii · 2011 · vol. 72(4) , pp. 7–12 · PMID:21086629 · W2395146097
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This study investigated morphological and molecular changes in adenomyosis foci concurrent with endometrial adenocarcinoma, finding increased expression of several markers correlating with higher atypia and adenocarcinoma development.

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Abstract

The purpose of the investigation was to study the morphological variants and molecular changes of the endothelial component of adenomyosis (AM) concurrent with endometrial adenocarcinoma (EAC). Monoclonal and polyclonal antibodies to ApoCas, Cl 2, 3, and 5, Ki-7, MMP-2, MMP-9, TIMP-1, E-cadherin, COX-2, EGFR, and VEGF were used as primary antibodies. The AM foci displayed the following types of epithelial changes: the epithelium corresponding to the proliferation stage; epithelial hyperplasia with and without atypia; atrophic epithelium. There was an increased expression of ApoCas, Ki-67, MMP-2, MMP-9, COX-2, VEGF, and EGFR, which increased from proliferation to hyperplasia with atypia. The maximum expression of the markers was seen in EAC. The foci of AM, which corresponded to epithelial hyperplasia with atypia, were characterized by the oncomarker changes supporting its malignant potential: elevated Ki-67 and EGRF, reduced E-cadherin, changes in MMP-2, MMP-9, TIMP-1, and claudins-2, -3, and -5.

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Condition tags

endometriosisadenomyosis

MeSH descriptors

Adenocarcinoma Adenocarcinoma Adenocarcinoma Adenocarcinoma Endometrial Neoplasms Endometrial Neoplasms Endometrial Neoplasms Endometrial Neoplasms Endometriosis Endometriosis Endometriosis Endometriosis Gene Expression Regulation, Neoplastic Neoplasm Proteins Adult Aged Antibodies, Monoclonal Antibodies, Monoclonal Epithelium Epithelium

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