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Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study

OBJECTIVE: Store operated calcium channels (SOCCs) and Receptor-operated calcium channels (ROCCs) are important pathways participating in regulation of intracellular Ca(2 +) concentration in various cell types. The purpose of our study is to determine whether genetic variations in key components of...

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Autores principales: Zhang, Zili, Wang, Jian, He, Jianxing, Zeng, Xiansheng, Chen, Xindong, Xiong, Mingmei, Zhou, Qipeng, Guo, Meihua, Li, Defu, Lu, Wenju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006132/
https://www.ncbi.nlm.nih.gov/pubmed/27617218
http://dx.doi.org/10.1016/j.mgene.2016.07.005
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author Zhang, Zili
Wang, Jian
He, Jianxing
Zeng, Xiansheng
Chen, Xindong
Xiong, Mingmei
Zhou, Qipeng
Guo, Meihua
Li, Defu
Lu, Wenju
author_facet Zhang, Zili
Wang, Jian
He, Jianxing
Zeng, Xiansheng
Chen, Xindong
Xiong, Mingmei
Zhou, Qipeng
Guo, Meihua
Li, Defu
Lu, Wenju
author_sort Zhang, Zili
collection PubMed
description OBJECTIVE: Store operated calcium channels (SOCCs) and Receptor-operated calcium channels (ROCCs) are important pathways participating in regulation of intracellular Ca(2 +) concentration in various cell types. The purpose of our study is to determine whether genetic variations in key components of SOCCs and ROCCs are associated with lung cancer risk. METHODS: We identified 236 tagSNPs in 9 key genes related to SOCCs and ROCCs (TRPC1, TRPC3, TRPC4, TRPC6, TRPC7, ORAI1, ORAI2, STIM1, and STIM2) and evaluated their association with lung cancer risk in a two-stage case-control study with a total of 2433 lung cancer cases and 2433 cancer-free controls using Illumina high throughput genotyping platform. RESULTS: We found consistently significant associations of TRPC4 rs9547991 and rs978156, and TRPC7 rs11748198 with increased risk of lung cancer among the three kinds of sources of populations (additive model in combined population: adjusted OR = 1.33, 95% CI = 1.11–1.59 for rs9547991; adjusted OR = 1.21, 95% CI = 1.08–1.35 for rs978156; and adjusted OR = 1.28, 95% CI = 1.10–1.47 for rs11748198). When combining the effects of TRPC7 rs11748198, and TRPC4 rs9547991 and rs978156, subjects carrying “≥ 1” variant alleles had a 1.29-fold increased risk of lung cancer (95% CI = 1.15–1.46), compared with those carrying “0” variant allele. Lung cancer risk significantly increased with the increasing number of variant alleles of the three SNPs in a dose-dependent manner (P for trend = 7.2 × 10(− 7)). CONCLUSION: These findings suggested that TRPC4 rs9547991 and rs978156, and TRPC7 rs11748198 were candidate susceptibility markers for lung cancer in Chinese population. Our study provides the epidemiological evidence supporting a connection between TRPC members and lung cancer risks.
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spelling pubmed-50061322016-09-09 Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study Zhang, Zili Wang, Jian He, Jianxing Zeng, Xiansheng Chen, Xindong Xiong, Mingmei Zhou, Qipeng Guo, Meihua Li, Defu Lu, Wenju Meta Gene Article OBJECTIVE: Store operated calcium channels (SOCCs) and Receptor-operated calcium channels (ROCCs) are important pathways participating in regulation of intracellular Ca(2 +) concentration in various cell types. The purpose of our study is to determine whether genetic variations in key components of SOCCs and ROCCs are associated with lung cancer risk. METHODS: We identified 236 tagSNPs in 9 key genes related to SOCCs and ROCCs (TRPC1, TRPC3, TRPC4, TRPC6, TRPC7, ORAI1, ORAI2, STIM1, and STIM2) and evaluated their association with lung cancer risk in a two-stage case-control study with a total of 2433 lung cancer cases and 2433 cancer-free controls using Illumina high throughput genotyping platform. RESULTS: We found consistently significant associations of TRPC4 rs9547991 and rs978156, and TRPC7 rs11748198 with increased risk of lung cancer among the three kinds of sources of populations (additive model in combined population: adjusted OR = 1.33, 95% CI = 1.11–1.59 for rs9547991; adjusted OR = 1.21, 95% CI = 1.08–1.35 for rs978156; and adjusted OR = 1.28, 95% CI = 1.10–1.47 for rs11748198). When combining the effects of TRPC7 rs11748198, and TRPC4 rs9547991 and rs978156, subjects carrying “≥ 1” variant alleles had a 1.29-fold increased risk of lung cancer (95% CI = 1.15–1.46), compared with those carrying “0” variant allele. Lung cancer risk significantly increased with the increasing number of variant alleles of the three SNPs in a dose-dependent manner (P for trend = 7.2 × 10(− 7)). CONCLUSION: These findings suggested that TRPC4 rs9547991 and rs978156, and TRPC7 rs11748198 were candidate susceptibility markers for lung cancer in Chinese population. Our study provides the epidemiological evidence supporting a connection between TRPC members and lung cancer risks. Elsevier 2016-07-08 /pmc/articles/PMC5006132/ /pubmed/27617218 http://dx.doi.org/10.1016/j.mgene.2016.07.005 Text en © 2016 Published by Elsevier B.V.
spellingShingle Article
Zhang, Zili
Wang, Jian
He, Jianxing
Zeng, Xiansheng
Chen, Xindong
Xiong, Mingmei
Zhou, Qipeng
Guo, Meihua
Li, Defu
Lu, Wenju
Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
title Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
title_full Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
title_fullStr Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
title_full_unstemmed Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
title_short Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
title_sort identification of trpcs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5006132/
https://www.ncbi.nlm.nih.gov/pubmed/27617218
http://dx.doi.org/10.1016/j.mgene.2016.07.005
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