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Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population
The tyrosine-protein kinase Tec (TEC) is a member of non-receptor tyrosine kinases and has critical roles in cell signaling transmission, calcium mobilization, gene expression, and transformation. TEC is also involved in various immune responses, such as mast cell activation. Therefore, we hypothesi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korea Genome Organization
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099349/ https://www.ncbi.nlm.nih.gov/pubmed/25031568 http://dx.doi.org/10.5808/GI.2014.12.2.58 |
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author | Lee, Jin Sol Bae, Joon Seol Park, Byung-Lae Cheong, Hyun Sub Kim, Jeong-Hyun Kim, Jason Yongha Namgoong, Suhg Kim, Ji-On Park, Choon-Sik Shin, Hyoung Doo |
author_facet | Lee, Jin Sol Bae, Joon Seol Park, Byung-Lae Cheong, Hyun Sub Kim, Jeong-Hyun Kim, Jason Yongha Namgoong, Suhg Kim, Ji-On Park, Choon-Sik Shin, Hyoung Doo |
author_sort | Lee, Jin Sol |
collection | PubMed |
description | The tyrosine-protein kinase Tec (TEC) is a member of non-receptor tyrosine kinases and has critical roles in cell signaling transmission, calcium mobilization, gene expression, and transformation. TEC is also involved in various immune responses, such as mast cell activation. Therefore, we hypothesized that TEC polymorphisms might be involved in aspirin-exacerbated respiratory disease (AERD) pathogenesis. We genotyped 38 TEC single nucleotide polymorphisms in a total of 592 subjects, which comprised 163 AERD cases and 429 aspirin-tolerant asthma controls. Logistic regression analysis was performed to examine the associations between TEC polymorphisms and the risk of AERD in a Korean population. The results revealed that TEC polymorphisms and major haplotypes were not associated with the risk of AERD. In another regression analysis for the fall rate of forced expiratory volume in 1 second (FEV(1)) by aspirin provocation, two variations (rs7664091 and rs12500534) and one haplotype (TEC_BL2_ht4) showed nominal associations with FEV(1) decline (p = 0.03-0.04). However, the association signals were not retained after performing corrections for multiple testing. Despite TEC playing an important role in immune responses, the results from the present study suggest that TEC polymorphisms do not affect AERD susceptibility. Findings from the present study might contribute to the genetic etiology of AERD pathogenesis. |
format | Online Article Text |
id | pubmed-4099349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korea Genome Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-40993492014-07-16 Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population Lee, Jin Sol Bae, Joon Seol Park, Byung-Lae Cheong, Hyun Sub Kim, Jeong-Hyun Kim, Jason Yongha Namgoong, Suhg Kim, Ji-On Park, Choon-Sik Shin, Hyoung Doo Genomics Inform Original Article The tyrosine-protein kinase Tec (TEC) is a member of non-receptor tyrosine kinases and has critical roles in cell signaling transmission, calcium mobilization, gene expression, and transformation. TEC is also involved in various immune responses, such as mast cell activation. Therefore, we hypothesized that TEC polymorphisms might be involved in aspirin-exacerbated respiratory disease (AERD) pathogenesis. We genotyped 38 TEC single nucleotide polymorphisms in a total of 592 subjects, which comprised 163 AERD cases and 429 aspirin-tolerant asthma controls. Logistic regression analysis was performed to examine the associations between TEC polymorphisms and the risk of AERD in a Korean population. The results revealed that TEC polymorphisms and major haplotypes were not associated with the risk of AERD. In another regression analysis for the fall rate of forced expiratory volume in 1 second (FEV(1)) by aspirin provocation, two variations (rs7664091 and rs12500534) and one haplotype (TEC_BL2_ht4) showed nominal associations with FEV(1) decline (p = 0.03-0.04). However, the association signals were not retained after performing corrections for multiple testing. Despite TEC playing an important role in immune responses, the results from the present study suggest that TEC polymorphisms do not affect AERD susceptibility. Findings from the present study might contribute to the genetic etiology of AERD pathogenesis. Korea Genome Organization 2014-06 2014-06-30 /pmc/articles/PMC4099349/ /pubmed/25031568 http://dx.doi.org/10.5808/GI.2014.12.2.58 Text en Copyright © 2014 by the Korea Genome Organization http://creativecommons.org/licenses/by-nc/3.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/). |
spellingShingle | Original Article Lee, Jin Sol Bae, Joon Seol Park, Byung-Lae Cheong, Hyun Sub Kim, Jeong-Hyun Kim, Jason Yongha Namgoong, Suhg Kim, Ji-On Park, Choon-Sik Shin, Hyoung Doo Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population |
title | Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population |
title_full | Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population |
title_fullStr | Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population |
title_full_unstemmed | Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population |
title_short | Association Analysis of TEC Polymorphisms with Aspirin-Exacerbated Respiratory Disease in a Korean Population |
title_sort | association analysis of tec polymorphisms with aspirin-exacerbated respiratory disease in a korean population |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099349/ https://www.ncbi.nlm.nih.gov/pubmed/25031568 http://dx.doi.org/10.5808/GI.2014.12.2.58 |
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