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Cancer heterogeneity: implications for targeted therapeutics

Developments in genomic techniques have provided insight into the remarkable genetic complexity of malignant tumours. There is increasing evidence that solid tumours may comprise of subpopulations of cells with distinct genomic alterations within the same tumour, a phenomenon termed intra-tumour het...

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Detalles Bibliográficos
Autores principales: Fisher, R, Pusztai, L, Swanton, C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593543/
https://www.ncbi.nlm.nih.gov/pubmed/23299535
http://dx.doi.org/10.1038/bjc.2012.581
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author Fisher, R
Pusztai, L
Swanton, C
author_facet Fisher, R
Pusztai, L
Swanton, C
author_sort Fisher, R
collection PubMed
description Developments in genomic techniques have provided insight into the remarkable genetic complexity of malignant tumours. There is increasing evidence that solid tumours may comprise of subpopulations of cells with distinct genomic alterations within the same tumour, a phenomenon termed intra-tumour heterogeneity. Intra-tumour heterogeneity is likely to have implications for cancer therapeutics and biomarker discovery, particularly in the era of targeted treatment, and evidence for a relationship between intra-tumoural heterogeneity and clinical outcome is emerging. Our understanding of the processes that exacerbate intra-tumoural heterogeneity, both iatrogenic and tumour specific, is likely to increase with the development and more widespread implementation of advanced sequencing technologies, and adaptation of clinical trial design to include comprehensive tissue collection protocols. The current evidence for intra-tumour heterogeneity and its relevance to cancer therapeutics will be presented in this mini-review.
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spelling pubmed-35935432013-03-11 Cancer heterogeneity: implications for targeted therapeutics Fisher, R Pusztai, L Swanton, C Br J Cancer Minireview Developments in genomic techniques have provided insight into the remarkable genetic complexity of malignant tumours. There is increasing evidence that solid tumours may comprise of subpopulations of cells with distinct genomic alterations within the same tumour, a phenomenon termed intra-tumour heterogeneity. Intra-tumour heterogeneity is likely to have implications for cancer therapeutics and biomarker discovery, particularly in the era of targeted treatment, and evidence for a relationship between intra-tumoural heterogeneity and clinical outcome is emerging. Our understanding of the processes that exacerbate intra-tumoural heterogeneity, both iatrogenic and tumour specific, is likely to increase with the development and more widespread implementation of advanced sequencing technologies, and adaptation of clinical trial design to include comprehensive tissue collection protocols. The current evidence for intra-tumour heterogeneity and its relevance to cancer therapeutics will be presented in this mini-review. Nature Publishing Group 2013-02-19 2013-01-08 /pmc/articles/PMC3593543/ /pubmed/23299535 http://dx.doi.org/10.1038/bjc.2012.581 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Minireview
Fisher, R
Pusztai, L
Swanton, C
Cancer heterogeneity: implications for targeted therapeutics
title Cancer heterogeneity: implications for targeted therapeutics
title_full Cancer heterogeneity: implications for targeted therapeutics
title_fullStr Cancer heterogeneity: implications for targeted therapeutics
title_full_unstemmed Cancer heterogeneity: implications for targeted therapeutics
title_short Cancer heterogeneity: implications for targeted therapeutics
title_sort cancer heterogeneity: implications for targeted therapeutics
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593543/
https://www.ncbi.nlm.nih.gov/pubmed/23299535
http://dx.doi.org/10.1038/bjc.2012.581
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