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Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far
Luminal Androgen Receptor Breast Cancers (LAR BCs) are characterized by a triple negative phenotype and by the expression of Androgen Receptor (AR), coupled with luminal-like genomic features. This unique BC subtype, accounting for about 10% of all triple negative BC, has raised considerable interes...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089148/ https://www.ncbi.nlm.nih.gov/pubmed/37056632 http://dx.doi.org/10.2147/OTT.S379867 |
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author | Stella, Stefania Martorana, Federica Massimino, Michele Vitale, Silvia Rita Manzella, Livia Vigneri, Paolo |
author_facet | Stella, Stefania Martorana, Federica Massimino, Michele Vitale, Silvia Rita Manzella, Livia Vigneri, Paolo |
author_sort | Stella, Stefania |
collection | PubMed |
description | Luminal Androgen Receptor Breast Cancers (LAR BCs) are characterized by a triple negative phenotype and by the expression of Androgen Receptor (AR), coupled with luminal-like genomic features. This unique BC subtype, accounting for about 10% of all triple negative BC, has raised considerable interest given its ill-defined clinical behavior and the chance to exploit AR as a therapeutic target. The complexity of AR activity in BC cells, as revealed by decades of mechanistic studies, holds promise to offer additional therapeutic options beyond mere AR inhibition. Indeed, preclinical and translational evidence showed that several pathways and mediators, including PI3K/mToR, HER2, BRCA1, cell cycle and immune modulation, can be tackled in LAR BCs. Moving from bench to bedside, several clinical trials tested anti-androgen therapies in LAR BCs, but their results are inconsistent and often disappointing. More recently, studies exploring combinations of anti-androgen agents with other targeted therapies have been designed and are currently ongoing. While the results from these trials are awaited, a concerted effort will be needed to find the biological vulnerabilities of LAR BCs which may disclose new and effective therapeutic targets, eventually improving patients’ outcomes. |
format | Online Article Text |
id | pubmed-10089148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-100891482023-04-12 Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far Stella, Stefania Martorana, Federica Massimino, Michele Vitale, Silvia Rita Manzella, Livia Vigneri, Paolo Onco Targets Ther Review Luminal Androgen Receptor Breast Cancers (LAR BCs) are characterized by a triple negative phenotype and by the expression of Androgen Receptor (AR), coupled with luminal-like genomic features. This unique BC subtype, accounting for about 10% of all triple negative BC, has raised considerable interest given its ill-defined clinical behavior and the chance to exploit AR as a therapeutic target. The complexity of AR activity in BC cells, as revealed by decades of mechanistic studies, holds promise to offer additional therapeutic options beyond mere AR inhibition. Indeed, preclinical and translational evidence showed that several pathways and mediators, including PI3K/mToR, HER2, BRCA1, cell cycle and immune modulation, can be tackled in LAR BCs. Moving from bench to bedside, several clinical trials tested anti-androgen therapies in LAR BCs, but their results are inconsistent and often disappointing. More recently, studies exploring combinations of anti-androgen agents with other targeted therapies have been designed and are currently ongoing. While the results from these trials are awaited, a concerted effort will be needed to find the biological vulnerabilities of LAR BCs which may disclose new and effective therapeutic targets, eventually improving patients’ outcomes. Dove 2023-04-07 /pmc/articles/PMC10089148/ /pubmed/37056632 http://dx.doi.org/10.2147/OTT.S379867 Text en © 2023 Stella et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Stella, Stefania Martorana, Federica Massimino, Michele Vitale, Silvia Rita Manzella, Livia Vigneri, Paolo Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far |
title | Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far |
title_full | Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far |
title_fullStr | Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far |
title_full_unstemmed | Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far |
title_short | Potential Therapeutic Targets for Luminal Androgen Receptor Breast Cancer: What We Know so Far |
title_sort | potential therapeutic targets for luminal androgen receptor breast cancer: what we know so far |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10089148/ https://www.ncbi.nlm.nih.gov/pubmed/37056632 http://dx.doi.org/10.2147/OTT.S379867 |
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