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Clinical variability and molecular heterogeneity in prostate cancer

Prostate cancer is a clinically heterogeneous disease, with some men having indolent disease that can safely be observed, while others have aggressive, lethal disease. Over the past decade, researchers have begun to unravel some of the genomic heterogeneity that contributes to these varying clinical...

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Detalles Bibliográficos
Autores principales: Shoag, Jonathan, Barbieri, Christopher E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955177/
https://www.ncbi.nlm.nih.gov/pubmed/27080479
http://dx.doi.org/10.4103/1008-682X.178852
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author Shoag, Jonathan
Barbieri, Christopher E
author_facet Shoag, Jonathan
Barbieri, Christopher E
author_sort Shoag, Jonathan
collection PubMed
description Prostate cancer is a clinically heterogeneous disease, with some men having indolent disease that can safely be observed, while others have aggressive, lethal disease. Over the past decade, researchers have begun to unravel some of the genomic heterogeneity that contributes to these varying clinical phenotypes. Distinct molecular sub-classes of prostate cancer have been identified, and the uniqueness of these sub-classes has been leveraged to predict clinical outcomes, design novel biomarkers for prostate cancer diagnosis, and develop novel therapeutics. Recent work has also elucidated the temporal and spatial heterogeneity of prostate cancer, helping us understand disease pathogenesis, response to therapy, and progression. New genomic techniques have provided us with a window into the remarkable clinical and genomic heterogeneity of prostate cancer, and this new perspective will increasingly impact patient care.
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spelling pubmed-49551772016-07-26 Clinical variability and molecular heterogeneity in prostate cancer Shoag, Jonathan Barbieri, Christopher E Asian J Androl Invited Review Prostate cancer is a clinically heterogeneous disease, with some men having indolent disease that can safely be observed, while others have aggressive, lethal disease. Over the past decade, researchers have begun to unravel some of the genomic heterogeneity that contributes to these varying clinical phenotypes. Distinct molecular sub-classes of prostate cancer have been identified, and the uniqueness of these sub-classes has been leveraged to predict clinical outcomes, design novel biomarkers for prostate cancer diagnosis, and develop novel therapeutics. Recent work has also elucidated the temporal and spatial heterogeneity of prostate cancer, helping us understand disease pathogenesis, response to therapy, and progression. New genomic techniques have provided us with a window into the remarkable clinical and genomic heterogeneity of prostate cancer, and this new perspective will increasingly impact patient care. Medknow Publications & Media Pvt Ltd 2016 2016-04-15 /pmc/articles/PMC4955177/ /pubmed/27080479 http://dx.doi.org/10.4103/1008-682X.178852 Text en Copyright: © Asian Journal of Andrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Invited Review
Shoag, Jonathan
Barbieri, Christopher E
Clinical variability and molecular heterogeneity in prostate cancer
title Clinical variability and molecular heterogeneity in prostate cancer
title_full Clinical variability and molecular heterogeneity in prostate cancer
title_fullStr Clinical variability and molecular heterogeneity in prostate cancer
title_full_unstemmed Clinical variability and molecular heterogeneity in prostate cancer
title_short Clinical variability and molecular heterogeneity in prostate cancer
title_sort clinical variability and molecular heterogeneity in prostate cancer
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955177/
https://www.ncbi.nlm.nih.gov/pubmed/27080479
http://dx.doi.org/10.4103/1008-682X.178852
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