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Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis
The intestinal epithelium has two distinct two stem cell populations, namely, crypt base columnar (CBC) cells and +4 cells. Several specific markers have been identified for each stem cell population. In this study, we examined the expression profiles of these markers in colitis-associated carcinoge...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529509/ https://www.ncbi.nlm.nih.gov/pubmed/28747693 http://dx.doi.org/10.1038/s41598-017-06900-x |
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author | Kim, Hye Sung Lee, Cheol Kim, Woo Ho Maeng, Young Hee Jang, Bo Gun |
author_facet | Kim, Hye Sung Lee, Cheol Kim, Woo Ho Maeng, Young Hee Jang, Bo Gun |
author_sort | Kim, Hye Sung |
collection | PubMed |
description | The intestinal epithelium has two distinct two stem cell populations, namely, crypt base columnar (CBC) cells and +4 cells. Several specific markers have been identified for each stem cell population. In this study, we examined the expression profiles of these markers in colitis-associated carcinogenesis (CAC) to investigate whether they can be used as biomarkers for the early detection of dysplasia. The expression of intestinal stem cell (ISC) markers was measured by real-time polymerase chain reaction during CAC that was induced by azoxymethane and dextran sodium sulfate treatment. CBC stem cell markers increased continuously with tumor development, whereas a +4 cell expression profile was not present. CBC stem cell population was suppressed in the acute colitis and then expanded to repopulate the crypts during the regeneration period. Notably, RNA in situ hybridization revealed that all dysplasia and cancer samples showed increased expression of CBC stem cell markers in more than one-third of the tumor height, whereas regenerative glands had CBC stem cell markers confined to the lower one-third of the crypt. These results suggest that CBC stem cell markers could be a useful tool for the early detection of colitis-induced tumors. |
format | Online Article Text |
id | pubmed-5529509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55295092017-08-02 Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis Kim, Hye Sung Lee, Cheol Kim, Woo Ho Maeng, Young Hee Jang, Bo Gun Sci Rep Article The intestinal epithelium has two distinct two stem cell populations, namely, crypt base columnar (CBC) cells and +4 cells. Several specific markers have been identified for each stem cell population. In this study, we examined the expression profiles of these markers in colitis-associated carcinogenesis (CAC) to investigate whether they can be used as biomarkers for the early detection of dysplasia. The expression of intestinal stem cell (ISC) markers was measured by real-time polymerase chain reaction during CAC that was induced by azoxymethane and dextran sodium sulfate treatment. CBC stem cell markers increased continuously with tumor development, whereas a +4 cell expression profile was not present. CBC stem cell population was suppressed in the acute colitis and then expanded to repopulate the crypts during the regeneration period. Notably, RNA in situ hybridization revealed that all dysplasia and cancer samples showed increased expression of CBC stem cell markers in more than one-third of the tumor height, whereas regenerative glands had CBC stem cell markers confined to the lower one-third of the crypt. These results suggest that CBC stem cell markers could be a useful tool for the early detection of colitis-induced tumors. Nature Publishing Group UK 2017-07-26 /pmc/articles/PMC5529509/ /pubmed/28747693 http://dx.doi.org/10.1038/s41598-017-06900-x Text en © The Author(s) 2017 Open Access 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 http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Hye Sung Lee, Cheol Kim, Woo Ho Maeng, Young Hee Jang, Bo Gun Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis |
title | Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis |
title_full | Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis |
title_fullStr | Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis |
title_full_unstemmed | Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis |
title_short | Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis |
title_sort | expression profile of intestinal stem cell markers in colitis-associated carcinogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529509/ https://www.ncbi.nlm.nih.gov/pubmed/28747693 http://dx.doi.org/10.1038/s41598-017-06900-x |
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