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Is mucinous carcinoma of the colorectum a distinct genetic entity?

Mucinous carcinomas are defined on the basis of the amount of the mucus component in the tumour mass. Apart from this quantitative criterion, a number of clinicopathological parameters (such as localisation, prevalence in different countries and age groups, association with HNPCC and inflammatory pr...

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Detalles Bibliográficos
Autor principal: Hanski, C.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1995
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034069/
https://www.ncbi.nlm.nih.gov/pubmed/8519644
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author Hanski, C.
author_facet Hanski, C.
author_sort Hanski, C.
collection PubMed
description Mucinous carcinomas are defined on the basis of the amount of the mucus component in the tumour mass. Apart from this quantitative criterion, a number of clinicopathological parameters (such as localisation, prevalence in different countries and age groups, association with HNPCC and inflammatory processes) and genetic alterations (e.g. frequency of mutation in Ki-ras and p53 genes, level of MUC2 expression) differentiate these tumours from the non-mucinous ones. Since a different set of genetic lesions implies different inducing agents, these observations suggest that there may be a 'mucinous pathway of carcinogenesis'. Further identification of genetic changes characteristic of the mucinous phenotype will help to understand the aetiology of these tumours and possibly establish markers for detection of the high-risk group.
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spelling pubmed-20340692009-09-10 Is mucinous carcinoma of the colorectum a distinct genetic entity? Hanski, C. Br J Cancer Research Article Mucinous carcinomas are defined on the basis of the amount of the mucus component in the tumour mass. Apart from this quantitative criterion, a number of clinicopathological parameters (such as localisation, prevalence in different countries and age groups, association with HNPCC and inflammatory processes) and genetic alterations (e.g. frequency of mutation in Ki-ras and p53 genes, level of MUC2 expression) differentiate these tumours from the non-mucinous ones. Since a different set of genetic lesions implies different inducing agents, these observations suggest that there may be a 'mucinous pathway of carcinogenesis'. Further identification of genetic changes characteristic of the mucinous phenotype will help to understand the aetiology of these tumours and possibly establish markers for detection of the high-risk group. Nature Publishing Group 1995-12 /pmc/articles/PMC2034069/ /pubmed/8519644 Text en 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 Research Article
Hanski, C.
Is mucinous carcinoma of the colorectum a distinct genetic entity?
title Is mucinous carcinoma of the colorectum a distinct genetic entity?
title_full Is mucinous carcinoma of the colorectum a distinct genetic entity?
title_fullStr Is mucinous carcinoma of the colorectum a distinct genetic entity?
title_full_unstemmed Is mucinous carcinoma of the colorectum a distinct genetic entity?
title_short Is mucinous carcinoma of the colorectum a distinct genetic entity?
title_sort is mucinous carcinoma of the colorectum a distinct genetic entity?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034069/
https://www.ncbi.nlm.nih.gov/pubmed/8519644
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