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Distribution of estrogen and progesterone receptors isoforms in endometrial cancer

BACKGROUND: 70–80% of sporadic endometrial carcinomas are defined as endometrioid carcinoma (EC). Early-stage, well differentiated endometrial carcinomas usually retain expression of estrogen and progesterone receptors (ER and PR, respectively), as advanced stage, poorly differentiated tumors often...

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Autores principales: Kreizman-Shefer, Hila, Pricop, Jana, Goldman, Shlomit, Elmalah, Irit, Shalev, Eliezer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022268/
https://www.ncbi.nlm.nih.gov/pubmed/24684970
http://dx.doi.org/10.1186/1746-1596-9-77
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author Kreizman-Shefer, Hila
Pricop, Jana
Goldman, Shlomit
Elmalah, Irit
Shalev, Eliezer
author_facet Kreizman-Shefer, Hila
Pricop, Jana
Goldman, Shlomit
Elmalah, Irit
Shalev, Eliezer
author_sort Kreizman-Shefer, Hila
collection PubMed
description BACKGROUND: 70–80% of sporadic endometrial carcinomas are defined as endometrioid carcinoma (EC). Early-stage, well differentiated endometrial carcinomas usually retain expression of estrogen and progesterone receptors (ER and PR, respectively), as advanced stage, poorly differentiated tumors often lack one or both of these receptors. Well-described EC prognosis includes tumor characteristics, such as depth of myometrial invasion. Therefore, in the current study, we evaluated the expression profile of ER and PR isoforms, including ER-α, PR-A and PR–B, in correlation to EC tumor histological depth. METHODS: Using immunohistochemistry and image analysis software, the expression of ER-α, PR-A, PR–B and Ki67 was assessed in endometrial stroma and epithelial glands of superficial, deep and extra-tumoral sections of 15 paraffin embedded EC specimens, and compared to 5 biopsies of non-malignant endometrium. RESULTS: Expression of PR-A and ER-α was found to be lower in EC compared to nonmalignant tissue, as the stromal expression was dramatically reduced compared to epithelial cells. Expression ratios of both receptors were significantly high in superficial and deep portions of EC; in non-tumoral portion of EC were close to the ratios of nonmalignant endometrium. PR-B expression was low in epithelial glands of EC superficial and deep portions, and high in the extra-tumoral region. Elevated PR-B expression was found in stroma of EC, as well. CONCLUSIONS: The ratio of ER-α and PR-A expression in the epithelial glands and the stroma of EC biopsies may serve as an additional parameter in the histological evaluation of EC tumor. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1155060506119016
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spelling pubmed-40222682014-05-16 Distribution of estrogen and progesterone receptors isoforms in endometrial cancer Kreizman-Shefer, Hila Pricop, Jana Goldman, Shlomit Elmalah, Irit Shalev, Eliezer Diagn Pathol Research BACKGROUND: 70–80% of sporadic endometrial carcinomas are defined as endometrioid carcinoma (EC). Early-stage, well differentiated endometrial carcinomas usually retain expression of estrogen and progesterone receptors (ER and PR, respectively), as advanced stage, poorly differentiated tumors often lack one or both of these receptors. Well-described EC prognosis includes tumor characteristics, such as depth of myometrial invasion. Therefore, in the current study, we evaluated the expression profile of ER and PR isoforms, including ER-α, PR-A and PR–B, in correlation to EC tumor histological depth. METHODS: Using immunohistochemistry and image analysis software, the expression of ER-α, PR-A, PR–B and Ki67 was assessed in endometrial stroma and epithelial glands of superficial, deep and extra-tumoral sections of 15 paraffin embedded EC specimens, and compared to 5 biopsies of non-malignant endometrium. RESULTS: Expression of PR-A and ER-α was found to be lower in EC compared to nonmalignant tissue, as the stromal expression was dramatically reduced compared to epithelial cells. Expression ratios of both receptors were significantly high in superficial and deep portions of EC; in non-tumoral portion of EC were close to the ratios of nonmalignant endometrium. PR-B expression was low in epithelial glands of EC superficial and deep portions, and high in the extra-tumoral region. Elevated PR-B expression was found in stroma of EC, as well. CONCLUSIONS: The ratio of ER-α and PR-A expression in the epithelial glands and the stroma of EC biopsies may serve as an additional parameter in the histological evaluation of EC tumor. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1155060506119016 BioMed Central 2014-03-31 /pmc/articles/PMC4022268/ /pubmed/24684970 http://dx.doi.org/10.1186/1746-1596-9-77 Text en Copyright © 2014 Kreizman-Shefer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kreizman-Shefer, Hila
Pricop, Jana
Goldman, Shlomit
Elmalah, Irit
Shalev, Eliezer
Distribution of estrogen and progesterone receptors isoforms in endometrial cancer
title Distribution of estrogen and progesterone receptors isoforms in endometrial cancer
title_full Distribution of estrogen and progesterone receptors isoforms in endometrial cancer
title_fullStr Distribution of estrogen and progesterone receptors isoforms in endometrial cancer
title_full_unstemmed Distribution of estrogen and progesterone receptors isoforms in endometrial cancer
title_short Distribution of estrogen and progesterone receptors isoforms in endometrial cancer
title_sort distribution of estrogen and progesterone receptors isoforms in endometrial cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022268/
https://www.ncbi.nlm.nih.gov/pubmed/24684970
http://dx.doi.org/10.1186/1746-1596-9-77
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