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Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis
Allergic rhinitis (AR) is a common inflammatory disease of the upper airway. Recent evidence suggests that gene-gene interactions between tumor necrosis factor receptor superfamily 4 (TNFSF4) and B cell lymphocyte kinase (BLK) may have a synergistic effect on T and B cells in determining immunologic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547929/ https://www.ncbi.nlm.nih.gov/pubmed/28713926 http://dx.doi.org/10.3892/mmr.2017.6954 |
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author | Shen, Yang Liu, Yun Wang, Xiao-Qiang Ke, Xia Kang, Hou-Yong Hong, Su-Ling |
author_facet | Shen, Yang Liu, Yun Wang, Xiao-Qiang Ke, Xia Kang, Hou-Yong Hong, Su-Ling |
author_sort | Shen, Yang |
collection | PubMed |
description | Allergic rhinitis (AR) is a common inflammatory disease of the upper airway. Recent evidence suggests that gene-gene interactions between tumor necrosis factor receptor superfamily 4 (TNFSF4) and B cell lymphocyte kinase (BLK) may have a synergistic effect on T and B cells in determining immunologic aberration, via the nuclear factor-κB pathway. The present study was performed to evaluate the potential association between specific single nucleotide polymorphisms (SNPs) in the TNFSF4 and BKL genes with susceptibility to AR in Chinese subjects. A population-based case-control study was performed in 600 Chinese AR patients and 700 controls. Blood was drawn for DNA extraction, and 9 SNPs (6 in TNFSF4 and 3 in BKL genes) were selected and genotyped. The TNFSF4 SNPs rs1234314 and rs1234315, and the BLK SNPs rs13277113 and rs1600249 were observed to occur in different frequencies between the AR patients and the controls. The CC (rs1234314, rs1234315) and AA (rs1600249, rs13277113) genotypes provided protective effects against AR, whereas the AG (rs13277113) genotype presented a risk factor for AR. The haplotypes ACC in the rs1234313-rs1234314-rs1234315 block and GA in the rs2254546-rs13277113 block significantly decreased the risk of AR, whereas the GGT and AG haplotypes served protective roles. SNP interaction analysis further indicated that there may be synergistic effects among the selected sets of polymorphisms. The present study suggests a novel association between specific TNFSF4 and BLK gene polymorphisms and AR risk, highlighting their potential utility as genetic biomarkers for AR susceptibility in a Chinese Han population. |
format | Online Article Text |
id | pubmed-5547929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-55479292017-10-24 Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis Shen, Yang Liu, Yun Wang, Xiao-Qiang Ke, Xia Kang, Hou-Yong Hong, Su-Ling Mol Med Rep Articles Allergic rhinitis (AR) is a common inflammatory disease of the upper airway. Recent evidence suggests that gene-gene interactions between tumor necrosis factor receptor superfamily 4 (TNFSF4) and B cell lymphocyte kinase (BLK) may have a synergistic effect on T and B cells in determining immunologic aberration, via the nuclear factor-κB pathway. The present study was performed to evaluate the potential association between specific single nucleotide polymorphisms (SNPs) in the TNFSF4 and BKL genes with susceptibility to AR in Chinese subjects. A population-based case-control study was performed in 600 Chinese AR patients and 700 controls. Blood was drawn for DNA extraction, and 9 SNPs (6 in TNFSF4 and 3 in BKL genes) were selected and genotyped. The TNFSF4 SNPs rs1234314 and rs1234315, and the BLK SNPs rs13277113 and rs1600249 were observed to occur in different frequencies between the AR patients and the controls. The CC (rs1234314, rs1234315) and AA (rs1600249, rs13277113) genotypes provided protective effects against AR, whereas the AG (rs13277113) genotype presented a risk factor for AR. The haplotypes ACC in the rs1234313-rs1234314-rs1234315 block and GA in the rs2254546-rs13277113 block significantly decreased the risk of AR, whereas the GGT and AG haplotypes served protective roles. SNP interaction analysis further indicated that there may be synergistic effects among the selected sets of polymorphisms. The present study suggests a novel association between specific TNFSF4 and BLK gene polymorphisms and AR risk, highlighting their potential utility as genetic biomarkers for AR susceptibility in a Chinese Han population. D.A. Spandidos 2017-09 2017-07-12 /pmc/articles/PMC5547929/ /pubmed/28713926 http://dx.doi.org/10.3892/mmr.2017.6954 Text en Copyright: © Shen et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Shen, Yang Liu, Yun Wang, Xiao-Qiang Ke, Xia Kang, Hou-Yong Hong, Su-Ling Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis |
title | Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis |
title_full | Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis |
title_fullStr | Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis |
title_full_unstemmed | Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis |
title_short | Association between TNFSF4 and BLK gene polymorphisms and susceptibility to allergic rhinitis |
title_sort | association between tnfsf4 and blk gene polymorphisms and susceptibility to allergic rhinitis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5547929/ https://www.ncbi.nlm.nih.gov/pubmed/28713926 http://dx.doi.org/10.3892/mmr.2017.6954 |
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