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Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma
Differential microsatellite instability (MSI) in tumour epithelial and stromal compartments has not been well examined for colorectal cancers. Using laser-captured microdissection, separate specimens of these compartments of 40 sporadic colorectal cancers were sampled and MSI was tested with four ma...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376921/ https://www.ncbi.nlm.nih.gov/pubmed/12915883 http://dx.doi.org/10.1038/sj.bjc.6601141 |
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author | Matsumoto, N Yoshida, T Yamashita, K Numata, Y Okayasu, I |
author_facet | Matsumoto, N Yoshida, T Yamashita, K Numata, Y Okayasu, I |
author_sort | Matsumoto, N |
collection | PubMed |
description | Differential microsatellite instability (MSI) in tumour epithelial and stromal compartments has not been well examined for colorectal cancers. Using laser-captured microdissection, separate specimens of these compartments of 40 sporadic colorectal cancers were sampled and MSI was tested with four markers. To examine the relation between the MSI phenotype in the stroma and other genetic events and histopathological features, p53 and K-ras gene mutations were analysed, and the expression of p53, hMLH1, and hMSH2 protein was determined by immunohistochemistry. Microsatellite instability positive results were obtained for both epithelium (34%) and stromal tissue (41%). While MSI in epithelium correlated with differentiation and Dukes' stage, that in stroma demonstrated an inverse relation, being particularly frequent in well-differentiated adenocarcinomas (54%) and Dukes' A lesions (55%). Further, a significant inverse correlation between p53 protein overexpression in the epithelium and MSI in the stroma was found (P=0.02475). The results suggest an alternative pathway of carcinogenesis involving stromal genetic instability in the development of colorectal cancers. |
format | Text |
id | pubmed-2376921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23769212009-09-10 Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma Matsumoto, N Yoshida, T Yamashita, K Numata, Y Okayasu, I Br J Cancer Genetics and Genomics Differential microsatellite instability (MSI) in tumour epithelial and stromal compartments has not been well examined for colorectal cancers. Using laser-captured microdissection, separate specimens of these compartments of 40 sporadic colorectal cancers were sampled and MSI was tested with four markers. To examine the relation between the MSI phenotype in the stroma and other genetic events and histopathological features, p53 and K-ras gene mutations were analysed, and the expression of p53, hMLH1, and hMSH2 protein was determined by immunohistochemistry. Microsatellite instability positive results were obtained for both epithelium (34%) and stromal tissue (41%). While MSI in epithelium correlated with differentiation and Dukes' stage, that in stroma demonstrated an inverse relation, being particularly frequent in well-differentiated adenocarcinomas (54%) and Dukes' A lesions (55%). Further, a significant inverse correlation between p53 protein overexpression in the epithelium and MSI in the stroma was found (P=0.02475). The results suggest an alternative pathway of carcinogenesis involving stromal genetic instability in the development of colorectal cancers. Nature Publishing Group 2003-08-18 2003-08-12 /pmc/articles/PMC2376921/ /pubmed/12915883 http://dx.doi.org/10.1038/sj.bjc.6601141 Text en Copyright © 2003 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 | Genetics and Genomics Matsumoto, N Yoshida, T Yamashita, K Numata, Y Okayasu, I Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma |
title | Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma |
title_full | Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma |
title_fullStr | Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma |
title_full_unstemmed | Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma |
title_short | Possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma |
title_sort | possible alternative carcinogenesis pathway featuring microsatellite instability in colorectal cancer stroma |
topic | Genetics and Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376921/ https://www.ncbi.nlm.nih.gov/pubmed/12915883 http://dx.doi.org/10.1038/sj.bjc.6601141 |
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