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Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer
INTRODUCTION: Colorectal cancer (CRC) is a highly heterogeneous disease, with pathologically similar cancers having completely different responses to treatment and patient survival. Intra-tumour heterogeneity (defined as distinct morphological and phenotypic differences) has recently been demonstrat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394146/ https://www.ncbi.nlm.nih.gov/pubmed/28097409 http://dx.doi.org/10.1007/s00268-016-3860-z |
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author | Jones, Huw Geraint Jenkins, Gareth Williams, Namor Griffiths, Paul Chambers, Phil Beynon, John Harris, Dean |
author_facet | Jones, Huw Geraint Jenkins, Gareth Williams, Namor Griffiths, Paul Chambers, Phil Beynon, John Harris, Dean |
author_sort | Jones, Huw Geraint |
collection | PubMed |
description | INTRODUCTION: Colorectal cancer (CRC) is a highly heterogeneous disease, with pathologically similar cancers having completely different responses to treatment and patient survival. Intra-tumour heterogeneity (defined as distinct morphological and phenotypic differences) has recently been demonstrated to be an important factor in the development and behaviour of cancer cells and can be used to determine response to anticancer therapy. METHOD: Patients with resected CRC had DNA extracted from eight defined tumour areas which were analysed for two genetic mutations (BRAF and KRAS) and one epigenetic trait (CpG island methylator phenotype/CIMP). Normal adjacent tissue was studied as control. RESULTS: Twelve patients with CRC were included. Intra-tumoural heterogeneity for KRAS mutation was seen in 2 patients (17%). There was no statistical evidence of CIMP status heterogeneity (p = 0.85), but 6 of the 12 patients (50%) demonstrated at least one heterogeneous area within the tumour. DISCUSSION: Intra-tumoural heterogeneity for both genetic and epigenetic factors in CRC is more prevalent than previously thought in Stage II and Stage III CRC. This study provides new insight into epigenetic heterogeneity of CRC and supports the development of a more targeted biopsy strategy to support expansion of personalised treatment. |
format | Online Article Text |
id | pubmed-5394146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-53941462017-05-03 Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer Jones, Huw Geraint Jenkins, Gareth Williams, Namor Griffiths, Paul Chambers, Phil Beynon, John Harris, Dean World J Surg Original Scientific Report INTRODUCTION: Colorectal cancer (CRC) is a highly heterogeneous disease, with pathologically similar cancers having completely different responses to treatment and patient survival. Intra-tumour heterogeneity (defined as distinct morphological and phenotypic differences) has recently been demonstrated to be an important factor in the development and behaviour of cancer cells and can be used to determine response to anticancer therapy. METHOD: Patients with resected CRC had DNA extracted from eight defined tumour areas which were analysed for two genetic mutations (BRAF and KRAS) and one epigenetic trait (CpG island methylator phenotype/CIMP). Normal adjacent tissue was studied as control. RESULTS: Twelve patients with CRC were included. Intra-tumoural heterogeneity for KRAS mutation was seen in 2 patients (17%). There was no statistical evidence of CIMP status heterogeneity (p = 0.85), but 6 of the 12 patients (50%) demonstrated at least one heterogeneous area within the tumour. DISCUSSION: Intra-tumoural heterogeneity for both genetic and epigenetic factors in CRC is more prevalent than previously thought in Stage II and Stage III CRC. This study provides new insight into epigenetic heterogeneity of CRC and supports the development of a more targeted biopsy strategy to support expansion of personalised treatment. Springer International Publishing 2017-01-17 2017 /pmc/articles/PMC5394146/ /pubmed/28097409 http://dx.doi.org/10.1007/s00268-016-3860-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Scientific Report Jones, Huw Geraint Jenkins, Gareth Williams, Namor Griffiths, Paul Chambers, Phil Beynon, John Harris, Dean Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer |
title | Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer |
title_full | Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer |
title_fullStr | Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer |
title_full_unstemmed | Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer |
title_short | Genetic and Epigenetic Intra-tumour Heterogeneity in Colorectal Cancer |
title_sort | genetic and epigenetic intra-tumour heterogeneity in colorectal cancer |
topic | Original Scientific Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394146/ https://www.ncbi.nlm.nih.gov/pubmed/28097409 http://dx.doi.org/10.1007/s00268-016-3860-z |
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