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Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance

Numerous growth-inducing signaling pathways have been implicated in the development of metastatic castrate-resistant prostate cancer, but their cross-talk with androgen receptor functions remains poorly understood. A recent study published in Science Signaling by Chen et al.(1) has identified a nove...

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Detalles Bibliográficos
Autores principales: Huang, Phoebe A., Price, Douglas K., Figg, William D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300349/
https://www.ncbi.nlm.nih.gov/pubmed/29757697
http://dx.doi.org/10.1080/15384047.2018.1449618
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author Huang, Phoebe A.
Price, Douglas K.
Figg, William D.
author_facet Huang, Phoebe A.
Price, Douglas K.
Figg, William D.
author_sort Huang, Phoebe A.
collection PubMed
description Numerous growth-inducing signaling pathways have been implicated in the development of metastatic castrate-resistant prostate cancer, but their cross-talk with androgen receptor functions remains poorly understood. A recent study published in Science Signaling by Chen et al.(1) has identified a novel androgen-mediated signaling axis driven by loss of SPDEF and gain of TGFBI to facilitate metastasis, which may explain the acquisition of resistance to androgen deprivation therapy. These findings suggest that therapeutic inhibition of androgen signaling may inadvertently promote castrate resistance by inhibiting tumor suppressive functions of the androgen receptor.
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spelling pubmed-63003492018-12-20 Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance Huang, Phoebe A. Price, Douglas K. Figg, William D. Cancer Biol Ther Journal Club Numerous growth-inducing signaling pathways have been implicated in the development of metastatic castrate-resistant prostate cancer, but their cross-talk with androgen receptor functions remains poorly understood. A recent study published in Science Signaling by Chen et al.(1) has identified a novel androgen-mediated signaling axis driven by loss of SPDEF and gain of TGFBI to facilitate metastasis, which may explain the acquisition of resistance to androgen deprivation therapy. These findings suggest that therapeutic inhibition of androgen signaling may inadvertently promote castrate resistance by inhibiting tumor suppressive functions of the androgen receptor. Taylor & Francis 2018-05-14 /pmc/articles/PMC6300349/ /pubmed/29757697 http://dx.doi.org/10.1080/15384047.2018.1449618 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Journal Club
Huang, Phoebe A.
Price, Douglas K.
Figg, William D.
Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance
title Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance
title_full Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance
title_fullStr Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance
title_full_unstemmed Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance
title_short Molecular drivers of metastatic castrate-resistant prostate cancer: New roads to resistance
title_sort molecular drivers of metastatic castrate-resistant prostate cancer: new roads to resistance
topic Journal Club
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300349/
https://www.ncbi.nlm.nih.gov/pubmed/29757697
http://dx.doi.org/10.1080/15384047.2018.1449618
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