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AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors

The co-expression of androgen (AR) and estrogen (ER) receptors, in terms of higher AR/ER ratio, has been recently associated with poor outcome in ER-positive (ER+) breast cancer (BC) patients. The aim of this study was to analyze if the biological aggressiveness, underlined in ER+ BC tumors with hig...

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Autores principales: Rangel, Nelson, Rondon-Lagos, Milena, Annaratone, Laura, Aristizábal-Pachon, Andrés Felipe, Cassoni, Paola, Sapino, Anna, Castellano, Isabella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226480/
https://www.ncbi.nlm.nih.gov/pubmed/32344660
http://dx.doi.org/10.3390/cells9041064
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author Rangel, Nelson
Rondon-Lagos, Milena
Annaratone, Laura
Aristizábal-Pachon, Andrés Felipe
Cassoni, Paola
Sapino, Anna
Castellano, Isabella
author_facet Rangel, Nelson
Rondon-Lagos, Milena
Annaratone, Laura
Aristizábal-Pachon, Andrés Felipe
Cassoni, Paola
Sapino, Anna
Castellano, Isabella
author_sort Rangel, Nelson
collection PubMed
description The co-expression of androgen (AR) and estrogen (ER) receptors, in terms of higher AR/ER ratio, has been recently associated with poor outcome in ER-positive (ER+) breast cancer (BC) patients. The aim of this study was to analyze if the biological aggressiveness, underlined in ER+ BC tumors with higher AR/ER ratio, could be due to higher expression of genes related to cell proliferation. On a cohort of 47 ER+ BC patients, the AR/ER ratio was assessed by immunohistochemistry and by mRNA analysis. The expression level of five gene proliferation markers was defined through TaqMan(®)-qPCR assays. Results were validated using 979 BC cases obtained from gene expression public databases. ER+ BC tumors with ratios of AR/ER ≥ 2 have higher expression levels of cellular proliferation genes than tumors with ratios of AR/ER < 2, in both the 47 ER+ BC patients (P < 0.001) and in the validation cohort (P = 0.005). Moreover, BC cases with ratios of AR/ER ≥ 2 of the validation cohort were mainly assigned to luminal B and HER2-enriched molecular subtypes, typically characterized by higher proliferation and poorer prognosis. These data suggest that joint routine evaluation of AR and ER expression may identify a unique subset of tumors, which show higher levels of cellular proliferation and therefore a more aggressive behavior.
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spelling pubmed-72264802020-05-18 AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors Rangel, Nelson Rondon-Lagos, Milena Annaratone, Laura Aristizábal-Pachon, Andrés Felipe Cassoni, Paola Sapino, Anna Castellano, Isabella Cells Article The co-expression of androgen (AR) and estrogen (ER) receptors, in terms of higher AR/ER ratio, has been recently associated with poor outcome in ER-positive (ER+) breast cancer (BC) patients. The aim of this study was to analyze if the biological aggressiveness, underlined in ER+ BC tumors with higher AR/ER ratio, could be due to higher expression of genes related to cell proliferation. On a cohort of 47 ER+ BC patients, the AR/ER ratio was assessed by immunohistochemistry and by mRNA analysis. The expression level of five gene proliferation markers was defined through TaqMan(®)-qPCR assays. Results were validated using 979 BC cases obtained from gene expression public databases. ER+ BC tumors with ratios of AR/ER ≥ 2 have higher expression levels of cellular proliferation genes than tumors with ratios of AR/ER < 2, in both the 47 ER+ BC patients (P < 0.001) and in the validation cohort (P = 0.005). Moreover, BC cases with ratios of AR/ER ≥ 2 of the validation cohort were mainly assigned to luminal B and HER2-enriched molecular subtypes, typically characterized by higher proliferation and poorer prognosis. These data suggest that joint routine evaluation of AR and ER expression may identify a unique subset of tumors, which show higher levels of cellular proliferation and therefore a more aggressive behavior. MDPI 2020-04-24 /pmc/articles/PMC7226480/ /pubmed/32344660 http://dx.doi.org/10.3390/cells9041064 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rangel, Nelson
Rondon-Lagos, Milena
Annaratone, Laura
Aristizábal-Pachon, Andrés Felipe
Cassoni, Paola
Sapino, Anna
Castellano, Isabella
AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors
title AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors
title_full AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors
title_fullStr AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors
title_full_unstemmed AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors
title_short AR/ER Ratio Correlates with Expression of Proliferation Markers and with Distinct Subset of Breast Tumors
title_sort ar/er ratio correlates with expression of proliferation markers and with distinct subset of breast tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226480/
https://www.ncbi.nlm.nih.gov/pubmed/32344660
http://dx.doi.org/10.3390/cells9041064
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