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Androgen receptor function and targeted therapeutics across breast cancer subtypes
Despite significant progress in breast cancer (BC) therapy, it is globally the most commonly diagnosed cancer and leads to the death of over 650,000 women annually. Androgen receptor (AR) is emerging as a potential new therapeutic target in BC. While the role of AR is well established in prostate ca...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664788/ https://www.ncbi.nlm.nih.gov/pubmed/36376977 http://dx.doi.org/10.1186/s13058-022-01574-4 |
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author | Kolyvas, Emily A. Caldas, Carlos Kelly, Kathleen Ahmad, Saif S. |
author_facet | Kolyvas, Emily A. Caldas, Carlos Kelly, Kathleen Ahmad, Saif S. |
author_sort | Kolyvas, Emily A. |
collection | PubMed |
description | Despite significant progress in breast cancer (BC) therapy, it is globally the most commonly diagnosed cancer and leads to the death of over 650,000 women annually. Androgen receptor (AR) is emerging as a potential new therapeutic target in BC. While the role of AR is well established in prostate cancer (PCa), its function in BC remains incompletely understood. Emerging data show that AR’s role in BC is dependent on several factors including, but not limited to, disease subtype, tumour microenvironment, and levels of circulating oestrogens and androgens. While targeting AR in PCa is becoming increasingly effective, these advances have yet to make any significant impact on the care of BC patients. However, this approach is increasingly being evaluated in BC and it is clear that improvements in our understanding of AR’s role in BC will increase the likelihood of success for AR-targeted therapies. This review summarizes our current understanding of the function of AR across BC subtypes. We highlight limitations in our current knowledge and demonstrate the importance of categorizing BC subtypes effectively, in relation to determining AR activity. Further, we describe the current state of the art regarding AR-targeted approaches for BC as monotherapy or in combination with radiotherapy. |
format | Online Article Text |
id | pubmed-9664788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96647882022-11-15 Androgen receptor function and targeted therapeutics across breast cancer subtypes Kolyvas, Emily A. Caldas, Carlos Kelly, Kathleen Ahmad, Saif S. Breast Cancer Res Review Despite significant progress in breast cancer (BC) therapy, it is globally the most commonly diagnosed cancer and leads to the death of over 650,000 women annually. Androgen receptor (AR) is emerging as a potential new therapeutic target in BC. While the role of AR is well established in prostate cancer (PCa), its function in BC remains incompletely understood. Emerging data show that AR’s role in BC is dependent on several factors including, but not limited to, disease subtype, tumour microenvironment, and levels of circulating oestrogens and androgens. While targeting AR in PCa is becoming increasingly effective, these advances have yet to make any significant impact on the care of BC patients. However, this approach is increasingly being evaluated in BC and it is clear that improvements in our understanding of AR’s role in BC will increase the likelihood of success for AR-targeted therapies. This review summarizes our current understanding of the function of AR across BC subtypes. We highlight limitations in our current knowledge and demonstrate the importance of categorizing BC subtypes effectively, in relation to determining AR activity. Further, we describe the current state of the art regarding AR-targeted approaches for BC as monotherapy or in combination with radiotherapy. BioMed Central 2022-11-14 2022 /pmc/articles/PMC9664788/ /pubmed/36376977 http://dx.doi.org/10.1186/s13058-022-01574-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Kolyvas, Emily A. Caldas, Carlos Kelly, Kathleen Ahmad, Saif S. Androgen receptor function and targeted therapeutics across breast cancer subtypes |
title | Androgen receptor function and targeted therapeutics across breast cancer subtypes |
title_full | Androgen receptor function and targeted therapeutics across breast cancer subtypes |
title_fullStr | Androgen receptor function and targeted therapeutics across breast cancer subtypes |
title_full_unstemmed | Androgen receptor function and targeted therapeutics across breast cancer subtypes |
title_short | Androgen receptor function and targeted therapeutics across breast cancer subtypes |
title_sort | androgen receptor function and targeted therapeutics across breast cancer subtypes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664788/ https://www.ncbi.nlm.nih.gov/pubmed/36376977 http://dx.doi.org/10.1186/s13058-022-01574-4 |
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