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Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity

Given the dearth of gene mutations in prostate cancer,12 it is likely that genomic rearrangements play a significant role in the evolution of prostate cancer. However, in the search for recurrent genomic alterations, “private alterations” have received less attention. Such alterations may provide in...

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Autores principales: Mendonca, Janet, Sharma, Anup, Kachhap, Sushant
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430943/
https://www.ncbi.nlm.nih.gov/pubmed/25532579
http://dx.doi.org/10.4103/1008-682X.143750
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author Mendonca, Janet
Sharma, Anup
Kachhap, Sushant
author_facet Mendonca, Janet
Sharma, Anup
Kachhap, Sushant
author_sort Mendonca, Janet
collection PubMed
description Given the dearth of gene mutations in prostate cancer,12 it is likely that genomic rearrangements play a significant role in the evolution of prostate cancer. However, in the search for recurrent genomic alterations, “private alterations” have received less attention. Such alterations may provide insights into the evolution, behavior, and clinical outcome of an individual tumor. In a recent report in “Genome Biology” Wyatt et al.3 defines unique alterations in a cohort of high-risk prostate cancer patient with a lethal phenotype. Utilizing a transcriptome sequencing approach they observe high inter-tumor heterogeneity; however, the genes altered distill into three distinct cancer-relevant pathways. Their analysis reveals the presence of several non-ETS fusions, which may contribute to the phenotype of individual tumors, and have significance for disease progression.
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spelling pubmed-44309432015-06-01 Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity Mendonca, Janet Sharma, Anup Kachhap, Sushant Asian J Androl Invited Research Highlight Given the dearth of gene mutations in prostate cancer,12 it is likely that genomic rearrangements play a significant role in the evolution of prostate cancer. However, in the search for recurrent genomic alterations, “private alterations” have received less attention. Such alterations may provide insights into the evolution, behavior, and clinical outcome of an individual tumor. In a recent report in “Genome Biology” Wyatt et al.3 defines unique alterations in a cohort of high-risk prostate cancer patient with a lethal phenotype. Utilizing a transcriptome sequencing approach they observe high inter-tumor heterogeneity; however, the genes altered distill into three distinct cancer-relevant pathways. Their analysis reveals the presence of several non-ETS fusions, which may contribute to the phenotype of individual tumors, and have significance for disease progression. Medknow Publications & Media Pvt Ltd 2015 2014-12-02 /pmc/articles/PMC4430943/ /pubmed/25532579 http://dx.doi.org/10.4103/1008-682X.143750 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Research Highlight
Mendonca, Janet
Sharma, Anup
Kachhap, Sushant
Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity
title Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity
title_full Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity
title_fullStr Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity
title_full_unstemmed Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity
title_short Transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity
title_sort transcriptome sequencing in prostate cancer identifies inter-tumor heterogeneity
topic Invited Research Highlight
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4430943/
https://www.ncbi.nlm.nih.gov/pubmed/25532579
http://dx.doi.org/10.4103/1008-682X.143750
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