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Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer

OBJECTIVES: The aim of the study was to estimate the implications of androgen receptor (AR) expression in estrogen receptor (ER)-positive subset of invasive breast carcinoma patients. PATIENTS AND METHODS: We assessed the AR expression in a subset of 96 predominantly ER-positive invasive breast carc...

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Autores principales: Agrawal, Anil, Ziolkowski, Piotr, Grzebieniak, Zygmunt, Jelen, Michal, Bobinski, Piotr, Agrawal, Siddarth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010278/
https://www.ncbi.nlm.nih.gov/pubmed/26230371
http://dx.doi.org/10.1097/PAI.0000000000000234
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author Agrawal, Anil
Ziolkowski, Piotr
Grzebieniak, Zygmunt
Jelen, Michal
Bobinski, Piotr
Agrawal, Siddarth
author_facet Agrawal, Anil
Ziolkowski, Piotr
Grzebieniak, Zygmunt
Jelen, Michal
Bobinski, Piotr
Agrawal, Siddarth
author_sort Agrawal, Anil
collection PubMed
description OBJECTIVES: The aim of the study was to estimate the implications of androgen receptor (AR) expression in estrogen receptor (ER)-positive subset of invasive breast carcinoma patients. PATIENTS AND METHODS: We assessed the AR expression in a subset of 96 predominantly ER-positive invasive breast carcinomas and correlated this expression pattern with several clinical and pathologic parameters: histologic type and grade, tumor size, lymph node status, progesterone receptor (PgR) status, and human epidermal growth factor receptor type 2 (HER2) overexpression and evaluated the association of these parameters with 10-year survival using univariate and multivariate analyses. Data used for analysis were derived from medical records. Immunohistochemical analysis for AR, ER, PgR, and HER2 were carried out and semiquantitative evaluation of stainings was performed. RESULTS: AR expression was demonstrated in 43.7% of patients. AR was significantly related to well-differentiated tumors and positive PgR/HER2 status. No statistical difference was demonstrated in AR expression in relation to tumor size, lymph node status, menopausal status, and tumor histologic type. AR expression was not an independent prognostic factor related to 10-year survival in ER-positive cancers. In multivariate analyses, older age at diagnosis, larger tumor size, and positive lymph node status were significantly associated with poorer 10-year survival. CONCLUSIONS: AR expression is significantly associated with ER/PgR/HER2 status and positively related to well-differentiated tumors. Although AR status in ER-positive cancers is not an independent prognostic factor, it might provide important additional information on prognosis and become a promising object for targeted therapy.
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spelling pubmed-50102782016-09-12 Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer Agrawal, Anil Ziolkowski, Piotr Grzebieniak, Zygmunt Jelen, Michal Bobinski, Piotr Agrawal, Siddarth Appl Immunohistochem Mol Morphol Research Articles OBJECTIVES: The aim of the study was to estimate the implications of androgen receptor (AR) expression in estrogen receptor (ER)-positive subset of invasive breast carcinoma patients. PATIENTS AND METHODS: We assessed the AR expression in a subset of 96 predominantly ER-positive invasive breast carcinomas and correlated this expression pattern with several clinical and pathologic parameters: histologic type and grade, tumor size, lymph node status, progesterone receptor (PgR) status, and human epidermal growth factor receptor type 2 (HER2) overexpression and evaluated the association of these parameters with 10-year survival using univariate and multivariate analyses. Data used for analysis were derived from medical records. Immunohistochemical analysis for AR, ER, PgR, and HER2 were carried out and semiquantitative evaluation of stainings was performed. RESULTS: AR expression was demonstrated in 43.7% of patients. AR was significantly related to well-differentiated tumors and positive PgR/HER2 status. No statistical difference was demonstrated in AR expression in relation to tumor size, lymph node status, menopausal status, and tumor histologic type. AR expression was not an independent prognostic factor related to 10-year survival in ER-positive cancers. In multivariate analyses, older age at diagnosis, larger tumor size, and positive lymph node status were significantly associated with poorer 10-year survival. CONCLUSIONS: AR expression is significantly associated with ER/PgR/HER2 status and positively related to well-differentiated tumors. Although AR status in ER-positive cancers is not an independent prognostic factor, it might provide important additional information on prognosis and become a promising object for targeted therapy. Lippincott Williams & Wilkins 2016-09 2016-08-30 /pmc/articles/PMC5010278/ /pubmed/26230371 http://dx.doi.org/10.1097/PAI.0000000000000234 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Research Articles
Agrawal, Anil
Ziolkowski, Piotr
Grzebieniak, Zygmunt
Jelen, Michal
Bobinski, Piotr
Agrawal, Siddarth
Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer
title Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer
title_full Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer
title_fullStr Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer
title_full_unstemmed Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer
title_short Expression of Androgen Receptor in Estrogen Receptor–positive Breast Cancer
title_sort expression of androgen receptor in estrogen receptor–positive breast cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010278/
https://www.ncbi.nlm.nih.gov/pubmed/26230371
http://dx.doi.org/10.1097/PAI.0000000000000234
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