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Advances in genetics: widening our understanding of prostate cancer

Prostate cancer is a leading cause of cancer-related death in Western men. Our understanding of the genetic alterations associated with disease predisposition, development, progression, and therapy response is rapidly improving, at least in part, owing to the development of next-generation sequencin...

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Detalles Bibliográficos
Autores principales: Pine, Angela C., Fioretti, Flavia F., Brooke, Greg N., Bevan, Charlotte L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926757/
https://www.ncbi.nlm.nih.gov/pubmed/27408704
http://dx.doi.org/10.12688/f1000research.8019.1
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author Pine, Angela C.
Fioretti, Flavia F.
Brooke, Greg N.
Bevan, Charlotte L.
author_facet Pine, Angela C.
Fioretti, Flavia F.
Brooke, Greg N.
Bevan, Charlotte L.
author_sort Pine, Angela C.
collection PubMed
description Prostate cancer is a leading cause of cancer-related death in Western men. Our understanding of the genetic alterations associated with disease predisposition, development, progression, and therapy response is rapidly improving, at least in part, owing to the development of next-generation sequencing technologies. Large advances have been made in our understanding of the genetics of prostate cancer through the application of whole-exome sequencing, and this review summarises recent advances in this field and discusses how exome sequencing could be used clinically to promote personalised medicine for prostate cancer patients.
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spelling pubmed-49267572016-07-11 Advances in genetics: widening our understanding of prostate cancer Pine, Angela C. Fioretti, Flavia F. Brooke, Greg N. Bevan, Charlotte L. F1000Res Review Prostate cancer is a leading cause of cancer-related death in Western men. Our understanding of the genetic alterations associated with disease predisposition, development, progression, and therapy response is rapidly improving, at least in part, owing to the development of next-generation sequencing technologies. Large advances have been made in our understanding of the genetics of prostate cancer through the application of whole-exome sequencing, and this review summarises recent advances in this field and discusses how exome sequencing could be used clinically to promote personalised medicine for prostate cancer patients. F1000Research 2016-06-27 /pmc/articles/PMC4926757/ /pubmed/27408704 http://dx.doi.org/10.12688/f1000research.8019.1 Text en Copyright: © 2016 Pine AC et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Pine, Angela C.
Fioretti, Flavia F.
Brooke, Greg N.
Bevan, Charlotte L.
Advances in genetics: widening our understanding of prostate cancer
title Advances in genetics: widening our understanding of prostate cancer
title_full Advances in genetics: widening our understanding of prostate cancer
title_fullStr Advances in genetics: widening our understanding of prostate cancer
title_full_unstemmed Advances in genetics: widening our understanding of prostate cancer
title_short Advances in genetics: widening our understanding of prostate cancer
title_sort advances in genetics: widening our understanding of prostate cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926757/
https://www.ncbi.nlm.nih.gov/pubmed/27408704
http://dx.doi.org/10.12688/f1000research.8019.1
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