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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2016
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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. |
format | Online Article Text |
id | pubmed-4926757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
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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