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Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications
Around 80–90% of prostate cancer (PCa) cases are dependent on androgens at initial diagnosis; hence, androgen ablation therapy directed toward a reduction in serum androgens and the inhibition of androgen receptor (AR) is generally the first therapy adopted. However, the patient’s response to androg...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763510/ https://www.ncbi.nlm.nih.gov/pubmed/33321757 http://dx.doi.org/10.3390/cells9122653 |
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author | Aurilio, Gaetano Cimadamore, Alessia Mazzucchelli, Roberta Lopez-Beltran, Antonio Verri, Elena Scarpelli, Marina Massari, Francesco Cheng, Liang Santoni, Matteo Montironi, Rodolfo |
author_facet | Aurilio, Gaetano Cimadamore, Alessia Mazzucchelli, Roberta Lopez-Beltran, Antonio Verri, Elena Scarpelli, Marina Massari, Francesco Cheng, Liang Santoni, Matteo Montironi, Rodolfo |
author_sort | Aurilio, Gaetano |
collection | PubMed |
description | Around 80–90% of prostate cancer (PCa) cases are dependent on androgens at initial diagnosis; hence, androgen ablation therapy directed toward a reduction in serum androgens and the inhibition of androgen receptor (AR) is generally the first therapy adopted. However, the patient’s response to androgen ablation therapy is variable, and 20–30% of PCa cases become castration resistant (CRPCa). Several mechanisms can guide treatment resistance to anti-AR molecules. In this regard, AR-dependent and -independent resistance mechanisms can be distinguished within the AR pathway. In this article, we investigate the multitude of AR signaling aspects, encompassing the biological structure of AR, current AR-targeted therapies, mechanisms driving resistance to AR, and AR crosstalk with other pathways, in an attempt to provide a comprehensive review for the PCa research community. We also summarize the new anti-AR drugs approved in non-metastatic castration-resistant PCa, in the castration-sensitive setting, and combination therapies with other drugs. |
format | Online Article Text |
id | pubmed-7763510 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77635102020-12-27 Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications Aurilio, Gaetano Cimadamore, Alessia Mazzucchelli, Roberta Lopez-Beltran, Antonio Verri, Elena Scarpelli, Marina Massari, Francesco Cheng, Liang Santoni, Matteo Montironi, Rodolfo Cells Review Around 80–90% of prostate cancer (PCa) cases are dependent on androgens at initial diagnosis; hence, androgen ablation therapy directed toward a reduction in serum androgens and the inhibition of androgen receptor (AR) is generally the first therapy adopted. However, the patient’s response to androgen ablation therapy is variable, and 20–30% of PCa cases become castration resistant (CRPCa). Several mechanisms can guide treatment resistance to anti-AR molecules. In this regard, AR-dependent and -independent resistance mechanisms can be distinguished within the AR pathway. In this article, we investigate the multitude of AR signaling aspects, encompassing the biological structure of AR, current AR-targeted therapies, mechanisms driving resistance to AR, and AR crosstalk with other pathways, in an attempt to provide a comprehensive review for the PCa research community. We also summarize the new anti-AR drugs approved in non-metastatic castration-resistant PCa, in the castration-sensitive setting, and combination therapies with other drugs. MDPI 2020-12-10 /pmc/articles/PMC7763510/ /pubmed/33321757 http://dx.doi.org/10.3390/cells9122653 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 | Review Aurilio, Gaetano Cimadamore, Alessia Mazzucchelli, Roberta Lopez-Beltran, Antonio Verri, Elena Scarpelli, Marina Massari, Francesco Cheng, Liang Santoni, Matteo Montironi, Rodolfo Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications |
title | Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications |
title_full | Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications |
title_fullStr | Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications |
title_full_unstemmed | Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications |
title_short | Androgen Receptor Signaling Pathway in Prostate Cancer: From Genetics to Clinical Applications |
title_sort | androgen receptor signaling pathway in prostate cancer: from genetics to clinical applications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7763510/ https://www.ncbi.nlm.nih.gov/pubmed/33321757 http://dx.doi.org/10.3390/cells9122653 |
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