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Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas
Microsatellite instability has been proposed as an alternative pathway of colorectal carcinogenesis. The aim of this study was to evaluate the interest of immunohistochemistry as a new tool for highlighting mismatch repair deficiency and to compare the results with a PCR-based microsatellite assay....
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376141/ https://www.ncbi.nlm.nih.gov/pubmed/12177776 http://dx.doi.org/10.1038/sj.bjc.6600474 |
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author | Chapusot, C Martin, L Bouvier, A M Bonithon-Kopp, C Ecarnot-Laubriet, A Rageot, D Ponnelle, T Laurent Puig, P Faivre, J Piard, F |
author_facet | Chapusot, C Martin, L Bouvier, A M Bonithon-Kopp, C Ecarnot-Laubriet, A Rageot, D Ponnelle, T Laurent Puig, P Faivre, J Piard, F |
author_sort | Chapusot, C |
collection | PubMed |
description | Microsatellite instability has been proposed as an alternative pathway of colorectal carcinogenesis. The aim of this study was to evaluate the interest of immunohistochemistry as a new tool for highlighting mismatch repair deficiency and to compare the results with a PCR-based microsatellite assay. A total of 100 sporadic proximal colon adenocarcinomas were analysed. The expression of hMLH1, hMSH2 and hMSH6 proteins evaluated by immunohistochemistry was altered in 39% of the cancers, whereas microsatellite instability assessed by PCR was detected in 43%. There was discordance between the two methods in eight cases. After further analyses performed on other tumoural areas for these eight cases, total concordance between the two techniques was observed (Kappa=100%). Our results demonstrate that immunohistochemistry may be as efficient as microsatellite amplification in the detection of unstable phenotype provided that at least two samples of each carcinoma are screened, because of intratumoural heterogeneity. British Journal of Cancer (2002) 87, 400–404. doi:10.1038/sj.bjc.6600474 www.bjcancer.com © 2002 Cancer Research UK |
format | Text |
id | pubmed-2376141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23761412009-09-10 Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas Chapusot, C Martin, L Bouvier, A M Bonithon-Kopp, C Ecarnot-Laubriet, A Rageot, D Ponnelle, T Laurent Puig, P Faivre, J Piard, F Br J Cancer Molecular and Cellular Pathology Microsatellite instability has been proposed as an alternative pathway of colorectal carcinogenesis. The aim of this study was to evaluate the interest of immunohistochemistry as a new tool for highlighting mismatch repair deficiency and to compare the results with a PCR-based microsatellite assay. A total of 100 sporadic proximal colon adenocarcinomas were analysed. The expression of hMLH1, hMSH2 and hMSH6 proteins evaluated by immunohistochemistry was altered in 39% of the cancers, whereas microsatellite instability assessed by PCR was detected in 43%. There was discordance between the two methods in eight cases. After further analyses performed on other tumoural areas for these eight cases, total concordance between the two techniques was observed (Kappa=100%). Our results demonstrate that immunohistochemistry may be as efficient as microsatellite amplification in the detection of unstable phenotype provided that at least two samples of each carcinoma are screened, because of intratumoural heterogeneity. British Journal of Cancer (2002) 87, 400–404. doi:10.1038/sj.bjc.6600474 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-08-12 /pmc/articles/PMC2376141/ /pubmed/12177776 http://dx.doi.org/10.1038/sj.bjc.6600474 Text en Copyright © 2002 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular and Cellular Pathology Chapusot, C Martin, L Bouvier, A M Bonithon-Kopp, C Ecarnot-Laubriet, A Rageot, D Ponnelle, T Laurent Puig, P Faivre, J Piard, F Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas |
title | Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas |
title_full | Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas |
title_fullStr | Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas |
title_full_unstemmed | Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas |
title_short | Microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas |
title_sort | microsatellite instability and intratumoural heterogeneity in 100 right-sided sporadic colon carcinomas |
topic | Molecular and Cellular Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376141/ https://www.ncbi.nlm.nih.gov/pubmed/12177776 http://dx.doi.org/10.1038/sj.bjc.6600474 |
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