Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis

Abstract 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...

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Main Authors: Hye Sung Kim, Cheol Lee, Woo Ho Kim, Young Hee Maeng, Bo Gun Jang
Format: Article
Language:English
Published: Nature Publishing Group 2017-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-06900-x
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spelling doaj-85953e3678274e40ae074975d1f1feec2020-12-08T00:53:49ZengNature Publishing GroupScientific Reports2045-23222017-07-017111110.1038/s41598-017-06900-xExpression profile of intestinal stem cell markers in colitis-associated carcinogenesisHye Sung Kim0Cheol Lee1Woo Ho Kim2Young Hee Maeng3Bo Gun Jang4Department of Pathology, Jeju National University School of MedicineDepartment of Pathology, Seoul National University College of MedicineDepartment of Pathology, Seoul National University College of MedicineDepartment of Pathology, Jeju National University School of MedicineDepartment of Pathology, Jeju National University School of MedicineAbstract 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.https://doi.org/10.1038/s41598-017-06900-x
collection DOAJ
language English
format Article
sources DOAJ
author Hye Sung Kim
Cheol Lee
Woo Ho Kim
Young Hee Maeng
Bo Gun Jang
spellingShingle Hye Sung Kim
Cheol Lee
Woo Ho Kim
Young Hee Maeng
Bo Gun Jang
Expression profile of intestinal stem cell markers in colitis-associated carcinogenesis
Scientific Reports
author_facet Hye Sung Kim
Cheol Lee
Woo Ho Kim
Young Hee Maeng
Bo Gun Jang
author_sort Hye Sung Kim
title 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_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_sort expression profile of intestinal stem cell markers in colitis-associated carcinogenesis
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-07-01
description Abstract 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.
url https://doi.org/10.1038/s41598-017-06900-x
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AT woohokim expressionprofileofintestinalstemcellmarkersincolitisassociatedcarcinogenesis
AT youngheemaeng expressionprofileofintestinalstemcellmarkersincolitisassociatedcarcinogenesis
AT bogunjang expressionprofileofintestinalstemcellmarkersincolitisassociatedcarcinogenesis
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