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AR-Signaling in Human Malignancies: Prostate Cancer and Beyond

In the 1940s Charles Huggins reported remarkable palliative benefits following surgical castration in men with advanced prostate cancer, and since then the androgen receptor (AR) has remained the main therapeutic target in this disease. Over the past couple of decades, our understanding of AR-signal...

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Detalles Bibliográficos
Autores principales: Schweizer, Michael T., Yu, Evan Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295778/
https://www.ncbi.nlm.nih.gov/pubmed/28085048
http://dx.doi.org/10.3390/cancers9010007
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author Schweizer, Michael T.
Yu, Evan Y.
author_facet Schweizer, Michael T.
Yu, Evan Y.
author_sort Schweizer, Michael T.
collection PubMed
description In the 1940s Charles Huggins reported remarkable palliative benefits following surgical castration in men with advanced prostate cancer, and since then the androgen receptor (AR) has remained the main therapeutic target in this disease. Over the past couple of decades, our understanding of AR-signaling biology has dramatically improved, and it has become apparent that the AR can modulate a number of other well-described oncogenic signaling pathways. Not surprisingly, mounting preclinical and epidemiologic data now supports a role for AR-signaling in promoting the growth and progression of several cancers other than prostate, and early phase clinical trials have documented preliminary signs of efficacy when AR-signaling inhibitors are used in several of these malignancies. In this article, we provide an overview of the evidence supporting the use of AR-directed therapies in prostate as well as other cancers, with an emphasis on the rationale for targeting AR-signaling across tumor types.
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spelling pubmed-52957782017-02-08 AR-Signaling in Human Malignancies: Prostate Cancer and Beyond Schweizer, Michael T. Yu, Evan Y. Cancers (Basel) Review In the 1940s Charles Huggins reported remarkable palliative benefits following surgical castration in men with advanced prostate cancer, and since then the androgen receptor (AR) has remained the main therapeutic target in this disease. Over the past couple of decades, our understanding of AR-signaling biology has dramatically improved, and it has become apparent that the AR can modulate a number of other well-described oncogenic signaling pathways. Not surprisingly, mounting preclinical and epidemiologic data now supports a role for AR-signaling in promoting the growth and progression of several cancers other than prostate, and early phase clinical trials have documented preliminary signs of efficacy when AR-signaling inhibitors are used in several of these malignancies. In this article, we provide an overview of the evidence supporting the use of AR-directed therapies in prostate as well as other cancers, with an emphasis on the rationale for targeting AR-signaling across tumor types. MDPI 2017-01-11 /pmc/articles/PMC5295778/ /pubmed/28085048 http://dx.doi.org/10.3390/cancers9010007 Text en © 2017 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
Schweizer, Michael T.
Yu, Evan Y.
AR-Signaling in Human Malignancies: Prostate Cancer and Beyond
title AR-Signaling in Human Malignancies: Prostate Cancer and Beyond
title_full AR-Signaling in Human Malignancies: Prostate Cancer and Beyond
title_fullStr AR-Signaling in Human Malignancies: Prostate Cancer and Beyond
title_full_unstemmed AR-Signaling in Human Malignancies: Prostate Cancer and Beyond
title_short AR-Signaling in Human Malignancies: Prostate Cancer and Beyond
title_sort ar-signaling in human malignancies: prostate cancer and beyond
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295778/
https://www.ncbi.nlm.nih.gov/pubmed/28085048
http://dx.doi.org/10.3390/cancers9010007
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