Literature DB >> 25445498

A common polymorphism in pre-miR-146a underlies Hirschsprung disease risk in Han Chinese.

Hairong Zhu1, Peng Cai1, Dongmei Zhu1, Chao Xu1, Hongxing Li1, Junwei Tang1, Hua Xie1, Yufeng Qin2, Ankur Sharan2, Weibing Tang3, Yankai Xia2.   

Abstract

BACKGROUND: Hirschsprung disease (HSCR) is a rare multigenic congenital disorder characterized by the absence of the enteric ganglia. To date, single nucleotide polymorphisms (SNPs) in pre-miRNAs have been confirmed related with some diseases. Thus, we hypothesized that pre-miRNA polymorphisms might contribute to HSCR susceptibility. We investigated whether rs2910164 and rs11614913 of pre-miR-146a and pre-miR-196a2, are associated with HSCR.
METHODS: Polymorphisms were genotyped using the Taqman method. Real-time PCR was used for detecting the expression level of miR-146a and its target gene ROBO1 in CC and GG genotypes.
RESULTS: Significant differences were found in the genotype distribution of rs2910164 and rs11614913 polymorphism between HSCR cases and controls (p = 0.023 and 0.041, respectively). Furthermore, G allele of rs2910164 might increase the risk of HSCR (OR, 1.54; 95% CI, 1.06-2.23). Moreover, the expression level of miR-146a for homozygote GG was also higher than homozygote CC (p = 0.0193). In contrast, the expression level of its target gene ROBO1 predicted in bioinformatics for homozygote GG was much lower than homozygote CC (p = 0.0096).
CONCLUSIONS: Our results showed that the polymorphism rs2910164 in pre-miR-146a might alter the production of mature miR-146a and then down-regulate the target gene ROBO1, which plays an important role in pathogenesis of HSCR.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hirschsprung disease; SNP; pre-miR-146a

Mesh:

Substances:

Year:  2014        PMID: 25445498     DOI: 10.1016/j.yexmp.2014.11.004

Source DB:  PubMed          Journal:  Exp Mol Pathol        ISSN: 0014-4800            Impact factor:   3.362


  8 in total

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6.  Suppressive action of miRNAs to ARP2/3 complex reduces cell migration and proliferation via RAC isoforms in Hirschsprung disease.

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7.  miRNA Profiling Reveals Dysregulation of RET and RET-Regulating Pathways in Hirschsprung's Disease.

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8.  IGF2-derived miR-483-3p associated with Hirschsprung's disease by targeting FHL1.

Authors:  Zhengke Zhi; Hairong Zhu; Xiaofeng Lv; Changgui Lu; Yang Li; Feng Wu; Lingling Zhou; Hongxing Li; Weibing Tang
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  8 in total

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