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AR Signaling in Human Malignancies: Prostate Cancer and Beyond

The notion that androgens and androgen receptor (AR) signaling are the hallmarks of prostate cancer oncogenesis and disease progression is generally well accepted. What is more poorly understood is the role of AR signaling in other human malignancies. This special issue of Cancers initially reviews...

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Detalles Bibliográficos
Autor principal: Antonarakis, Emmanuel S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789372/
https://www.ncbi.nlm.nih.gov/pubmed/29346310
http://dx.doi.org/10.3390/cancers10010022
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author Antonarakis, Emmanuel S.
author_facet Antonarakis, Emmanuel S.
author_sort Antonarakis, Emmanuel S.
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description The notion that androgens and androgen receptor (AR) signaling are the hallmarks of prostate cancer oncogenesis and disease progression is generally well accepted. What is more poorly understood is the role of AR signaling in other human malignancies. This special issue of Cancers initially reviews the role of AR in advanced prostate cancer, and then explores the potential importance of AR signaling in other epithelial malignancies. The first few articles focus on the use of novel AR-targeting therapies in castration-resistant prostate cancer and the mechanisms of resistance to novel antiandrogens, and they also outline the interaction between AR and other cellular pathways, including PI3 kinase signaling, transcriptional regulation, angiogenesis, stromal factors, Wnt signaling, and epigenetic regulation in prostate cancer. The next several articles review the possible role of androgens and AR signaling in breast cancer, bladder cancer, salivary gland cancer, and hepatocellular carcinoma, as well as the potential treatment implications of using antiandrogen therapies in these non-prostatic malignancies.
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spelling pubmed-57893722018-02-02 AR Signaling in Human Malignancies: Prostate Cancer and Beyond Antonarakis, Emmanuel S. Cancers (Basel) Editorial The notion that androgens and androgen receptor (AR) signaling are the hallmarks of prostate cancer oncogenesis and disease progression is generally well accepted. What is more poorly understood is the role of AR signaling in other human malignancies. This special issue of Cancers initially reviews the role of AR in advanced prostate cancer, and then explores the potential importance of AR signaling in other epithelial malignancies. The first few articles focus on the use of novel AR-targeting therapies in castration-resistant prostate cancer and the mechanisms of resistance to novel antiandrogens, and they also outline the interaction between AR and other cellular pathways, including PI3 kinase signaling, transcriptional regulation, angiogenesis, stromal factors, Wnt signaling, and epigenetic regulation in prostate cancer. The next several articles review the possible role of androgens and AR signaling in breast cancer, bladder cancer, salivary gland cancer, and hepatocellular carcinoma, as well as the potential treatment implications of using antiandrogen therapies in these non-prostatic malignancies. MDPI 2018-01-18 /pmc/articles/PMC5789372/ /pubmed/29346310 http://dx.doi.org/10.3390/cancers10010022 Text en © 2018 by the author. 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 Editorial
Antonarakis, Emmanuel S.
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 Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789372/
https://www.ncbi.nlm.nih.gov/pubmed/29346310
http://dx.doi.org/10.3390/cancers10010022
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