Literature DB >> 18668679

Runt-related transcription factor 3 is associated with ulcerative colitis and shows epistasis with solute carrier family 22, members 4 and 5.

Rinse K Weersma1, Lu Zhou, Ilja M Nolte, Gerrit van der Steege, Hendrik M van Dullemen, Elvira Oosterom, Lisette Bok, Maikel P Peppelenbosch, Klaas N Faber, Jan H Kleibeuker, Gerard Dijkstra.   

Abstract

BACKGROUND: Inflammatory bowel disease (IBD), comprising Crohn's disease (CD) and ulcerative colitis (UC), are intestinal inflammatory disorders with a complex genetic background. Mice deficient for the runt-domain-transcription-factor3 (Runx3) develop spontaneous colitis. Human RUNX3 resides in an IBD-susceptibility locus. We studied the association of RUNX3 in a cohort of IBD patients and analyzed the interaction with SLC22A4/5. RUNX3 and OCTN1 mRNA expression was assessed in inflamed and noninflamed mucosa from patients and controls.
METHODS: 543 IBD patients (309 CD / 234 UC) and 296 controls were included. Four single nucleotide polymorphisms (SNPs) and 4 microsatellite markers were studied for RUNX3. Five SNPs (including SNP-207G-->C and SNP1672C-->T) were analyzed for SLC22A4/5. RUNX3, and OCTN1 expression in mucosal tissue from 30 patients (14 UC / 16 CD) and 6 controls were determined by quantitative polymerase chain reaction.
RESULTS: A significant association between RUNX3-SNP rs2236851 and UC (OR 1.61; 95% confidence interval [CI] 1.11-2.32, P = 0.020) was found. Carriership is associated with pancolitis (odds ratio [OR] 1.86; 95% CI 1.08-3.21). SLC22A4/5-SNPs rs272893 and rs273900 are associated with CD (OR 2.16; 95% CI 1.21-3.59 and OR 2.40; 95% CI 1.43-4.05). We found epistasis for carriership of a risk-associated allele in RUNX3 and SLC22A4/5 for UC patients versus CD patients (OR 3.83; 95% CI 1.26-11.67). RUNX3 mRNA expression is increased (P = 0.01) in inflamed colonic mucosa of UC patients compared to noninflamed mucosa and controls.
CONCLUSIONS: We provide evidence for the genetic association of RUNX3 with UC and for CD with the IBD5 locus including SLC22A4/5. An epistatic effect of RUNX3 and SLC22A4 was associated with an increased risk for UC. Our data suggest a role for RUNX3 in UC susceptibility.

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Year:  2008        PMID: 18668679     DOI: 10.1002/ibd.20610

Source DB:  PubMed          Journal:  Inflamm Bowel Dis        ISSN: 1078-0998            Impact factor:   5.325


  11 in total

Review 1.  The RUNX complex: reaching beyond haematopoiesis into immunity.

Authors:  Dominic Chih-Cheng Voon; Yit Teng Hor; Yoshiaki Ito
Journal:  Immunology       Date:  2015-10-25       Impact factor: 7.397

2.  Haplotype in the IBD5 region is associated with refractory Crohn's disease in Slovenian patients and modulates expression of the SLC22A5 gene.

Authors:  Katja Repnik; Uroš Potočnik
Journal:  J Gastroenterol       Date:  2011-06-22       Impact factor: 7.527

3.  Association between OCTN1/2 gene polymorphisms (1672C-T, 207G-C) and susceptibility of Crohn's disease: a meta-analysis.

Authors:  Chao Xuan; Bei-Bei Zhang; Tao Yang; Kai-Feng Deng; Ming Li; Rui-Juan Tian
Journal:  Int J Colorectal Dis       Date:  2011-06-25       Impact factor: 2.571

4.  RUNX3 is up-regulated in abdominal aortic aneurysm and regulates the function of vascular smooth muscle cells by regulating TGF-β1.

Authors:  Zhongxiao Zhou; Haimeng Zhou; Xin Zou; Xiaowei Wang
Journal:  J Mol Histol       Date:  2021-11-23       Impact factor: 3.156

Review 5.  Genetically engineered mouse models for studying inflammatory bowel disease.

Authors:  Atsushi Mizoguchi; Takahito Takeuchi; Hidetomo Himuro; Toshiyuki Okada; Emiko Mizoguchi
Journal:  J Pathol       Date:  2015-11-14       Impact factor: 7.996

6.  Transcription Factors That Regulate the Pathogenesis of Ulcerative Colitis.

Authors:  Bing Zhang; Tao Sun
Journal:  Biomed Res Int       Date:  2020-08-24       Impact factor: 3.411

7.  Validation of epigenetic markers to identify colitis associated cancer: Results of module 1 of the ENDCAP-C study.

Authors:  Andrew D Beggs; Samir Mehta; Jonathan J Deeks; Jonathan D James; Germaine M Caldwell; Mark P Dilworth; Joanne D Stockton; Daniel Blakeway; Valerie Pestinger; Alexandra Vince; Phillipe Taniere; Tariq Iqbal; Laura Magill; Glenn Matthews; Dion G Morton
Journal:  EBioMedicine       Date:  2018-11-22       Impact factor: 8.143

8.  A dual role for DNA binding by Runt in activation and repression of sloppy paired transcription.

Authors:  Lisa Prazak; Yasuno Iwasaki; Ah-Ram Kim; Konstantin Kozlov; Kevin King; J Peter Gergen
Journal:  Mol Biol Cell       Date:  2021-08-25       Impact factor: 4.138

9.  Runx3 specifies lineage commitment of innate lymphoid cells.

Authors:  Takashi Ebihara; Christina Song; Stacy H Ryu; Beatrice Plougastel-Douglas; Liping Yang; Ditsa Levanon; Yoram Groner; Michael D Bern; Thaddeus S Stappenbeck; Marco Colonna; Takeshi Egawa; Wayne M Yokoyama
Journal:  Nat Immunol       Date:  2015-09-28       Impact factor: 25.606

10.  ERAP1/ERAP2 and RUNX3 polymorphisms are not associated with ankylosing spondylitis susceptibility in Chinese Han.

Authors:  W Su; L Du; S Liu; J Deng; Q Cao; G Yuan; A Kijlstra; P Yang
Journal:  Clin Exp Immunol       Date:  2018-03-30       Impact factor: 4.330

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