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CEACAM6 Gene Variants in Inflammatory Bowel Disease

BACKGROUND: The carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) acts as a receptor for adherent-invasive E. coli (AIEC) and its ileal expression is increased in patients with Crohn's disease (CD). Given its contribution to the pathogenesis of CD, we aimed to investigate the...

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Autores principales: Glas, Jürgen, Seiderer, Julia, Fries, Christoph, Tillack, Cornelia, Pfennig, Simone, Weidinger, Maria, Beigel, Florian, Olszak, Torsten, Lass, Ulrich, Göke, Burkhard, Ochsenkühn, Thomas, Wolf, Christiane, Lohse, Peter, Müller-Myhsok, Bertram, Diegelmann, Julia, Czamara, Darina, Brand, Stephan
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084820/
https://www.ncbi.nlm.nih.gov/pubmed/21559399
http://dx.doi.org/10.1371/journal.pone.0019319
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author Glas, Jürgen
Seiderer, Julia
Fries, Christoph
Tillack, Cornelia
Pfennig, Simone
Weidinger, Maria
Beigel, Florian
Olszak, Torsten
Lass, Ulrich
Göke, Burkhard
Ochsenkühn, Thomas
Wolf, Christiane
Lohse, Peter
Müller-Myhsok, Bertram
Diegelmann, Julia
Czamara, Darina
Brand, Stephan
author_facet Glas, Jürgen
Seiderer, Julia
Fries, Christoph
Tillack, Cornelia
Pfennig, Simone
Weidinger, Maria
Beigel, Florian
Olszak, Torsten
Lass, Ulrich
Göke, Burkhard
Ochsenkühn, Thomas
Wolf, Christiane
Lohse, Peter
Müller-Myhsok, Bertram
Diegelmann, Julia
Czamara, Darina
Brand, Stephan
author_sort Glas, Jürgen
collection PubMed
description BACKGROUND: The carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) acts as a receptor for adherent-invasive E. coli (AIEC) and its ileal expression is increased in patients with Crohn's disease (CD). Given its contribution to the pathogenesis of CD, we aimed to investigate the role of genetic variants in the CEACAM6 region in patients with inflammatory bowel diseases (IBD). METHODOLOGY: In this study, a total of 2,683 genomic DNA samples (including DNA from 858 CD patients, 475 patients with ulcerative colitis (UC), and 1,350 healthy, unrelated controls) was analyzed for eight CEACAM6 SNPs (rs10415946, rs1805223 = p.Pro42Pro, rs4803507, rs4803508, rs11548735 = p.Gly239Val, rs7246116 = pHis260His, rs2701, rs10416839). In addition, a detailed haplotype analysis and genotype-phenotype analysis were performed. Overall, our genotype analysis did not reveal any significant association of the investigated CEACAM6 SNPs and haplotypes with CD or UC susceptibility, although certain CEACAM6 SNPs modulated CEACAM6 expression in intestinal epithelial cell lines. Despite its function as receptor of AIEC in ileal CD, we found no association of the CEACAM6 SNPs with ileal or ileocolonic CD. Moreover, there was no evidence of epistasis between the analyzed CEACAM6 variants and the main CD-associated NOD2, IL23R and ATG16L1 variants. CONCLUSIONS: This study represents the first detailed analysis of CEACAM6 variants in IBD patients. Despite its important role in bacterial attachment in ileal CD, we could not demonstrate a role for CEACAM6 variants in IBD susceptibility or regarding an ileal CD phenotype. Further functional studies are required to analyze if these gene variants modulate ileal bacterial attachment.
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spelling pubmed-30848202011-05-10 CEACAM6 Gene Variants in Inflammatory Bowel Disease Glas, Jürgen Seiderer, Julia Fries, Christoph Tillack, Cornelia Pfennig, Simone Weidinger, Maria Beigel, Florian Olszak, Torsten Lass, Ulrich Göke, Burkhard Ochsenkühn, Thomas Wolf, Christiane Lohse, Peter Müller-Myhsok, Bertram Diegelmann, Julia Czamara, Darina Brand, Stephan PLoS One Research Article BACKGROUND: The carcinoembryonic antigen-related cell adhesion molecule 6 (CEACAM6) acts as a receptor for adherent-invasive E. coli (AIEC) and its ileal expression is increased in patients with Crohn's disease (CD). Given its contribution to the pathogenesis of CD, we aimed to investigate the role of genetic variants in the CEACAM6 region in patients with inflammatory bowel diseases (IBD). METHODOLOGY: In this study, a total of 2,683 genomic DNA samples (including DNA from 858 CD patients, 475 patients with ulcerative colitis (UC), and 1,350 healthy, unrelated controls) was analyzed for eight CEACAM6 SNPs (rs10415946, rs1805223 = p.Pro42Pro, rs4803507, rs4803508, rs11548735 = p.Gly239Val, rs7246116 = pHis260His, rs2701, rs10416839). In addition, a detailed haplotype analysis and genotype-phenotype analysis were performed. Overall, our genotype analysis did not reveal any significant association of the investigated CEACAM6 SNPs and haplotypes with CD or UC susceptibility, although certain CEACAM6 SNPs modulated CEACAM6 expression in intestinal epithelial cell lines. Despite its function as receptor of AIEC in ileal CD, we found no association of the CEACAM6 SNPs with ileal or ileocolonic CD. Moreover, there was no evidence of epistasis between the analyzed CEACAM6 variants and the main CD-associated NOD2, IL23R and ATG16L1 variants. CONCLUSIONS: This study represents the first detailed analysis of CEACAM6 variants in IBD patients. Despite its important role in bacterial attachment in ileal CD, we could not demonstrate a role for CEACAM6 variants in IBD susceptibility or regarding an ileal CD phenotype. Further functional studies are required to analyze if these gene variants modulate ileal bacterial attachment. Public Library of Science 2011-04-29 /pmc/articles/PMC3084820/ /pubmed/21559399 http://dx.doi.org/10.1371/journal.pone.0019319 Text en Glas et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Glas, Jürgen
Seiderer, Julia
Fries, Christoph
Tillack, Cornelia
Pfennig, Simone
Weidinger, Maria
Beigel, Florian
Olszak, Torsten
Lass, Ulrich
Göke, Burkhard
Ochsenkühn, Thomas
Wolf, Christiane
Lohse, Peter
Müller-Myhsok, Bertram
Diegelmann, Julia
Czamara, Darina
Brand, Stephan
CEACAM6 Gene Variants in Inflammatory Bowel Disease
title CEACAM6 Gene Variants in Inflammatory Bowel Disease
title_full CEACAM6 Gene Variants in Inflammatory Bowel Disease
title_fullStr CEACAM6 Gene Variants in Inflammatory Bowel Disease
title_full_unstemmed CEACAM6 Gene Variants in Inflammatory Bowel Disease
title_short CEACAM6 Gene Variants in Inflammatory Bowel Disease
title_sort ceacam6 gene variants in inflammatory bowel disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3084820/
https://www.ncbi.nlm.nih.gov/pubmed/21559399
http://dx.doi.org/10.1371/journal.pone.0019319
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