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ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis
Rs189037 (G>A) is an important functional variant with ataxia telangiectasia mutated (ATM) gene, which might affect ATM’s expression involvement in several human cancers. Increasing evidence reveals that smoking-related cancers have distinct molecular characteristics from non-smoking cancers. Unt...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6597848/ https://www.ncbi.nlm.nih.gov/pubmed/31201228 http://dx.doi.org/10.1042/BSR20191298 |
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author | He, Xiaoxia Wang, Peng Li, Ying Shen, Na |
author_facet | He, Xiaoxia Wang, Peng Li, Ying Shen, Na |
author_sort | He, Xiaoxia |
collection | PubMed |
description | Rs189037 (G>A) is an important functional variant with ataxia telangiectasia mutated (ATM) gene, which might affect ATM’s expression involvement in several human cancers. Increasing evidence reveals that smoking-related cancers have distinct molecular characteristics from non-smoking cancers. Until now, the role of ATM rs189037 in cancer risk stratified by smoking status still remains unclear. To evaluate the association between ATM rs189037 and cancer risk based on smoking status, we performed this meta-analysis by a comprehensive literature search via databases of PubMed, Embase, Web of Science and CNKI, updated till January 2019. Multivariate-adjusted odds ratios (ORs) and 95% confidence intervals (CIs) were extracted from eligible studies if available, to assess the relationship strengths. A total of seven eligible studies were included, comprising 4294 cancer patients (smokers: 1744 [40.6%]) and 4259 controls (smokers: 1418 [33.3%]). Results indicated a significant association of ATM rs189037 with cancer risk. In non-smokers, compared with GG genotype, AA genotype increased a 1.40-fold risk of overall cancer (OR = 1.40, 95% CI = 1.15–1.70, P(heterogeneity)=0.433, I(2) = 0.0%). Subgroup analysis in lung cancer (LC) also exhibited a significant result (OR = 1.41, 95% CI = 1.15–1.73, P(heterogeneity)=0.306, I(2) = 17.0%) only in non-smokers. However, the association was not observed in smokers, no matter for overall cancer or for LC. Our findings highlight that ATM rs189037 significantly increases cancer susceptibility in non-smokers, rather than in smokers. The association is prominent in LC. |
format | Online Article Text |
id | pubmed-6597848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65978482019-07-05 ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis He, Xiaoxia Wang, Peng Li, Ying Shen, Na Biosci Rep Research Articles Rs189037 (G>A) is an important functional variant with ataxia telangiectasia mutated (ATM) gene, which might affect ATM’s expression involvement in several human cancers. Increasing evidence reveals that smoking-related cancers have distinct molecular characteristics from non-smoking cancers. Until now, the role of ATM rs189037 in cancer risk stratified by smoking status still remains unclear. To evaluate the association between ATM rs189037 and cancer risk based on smoking status, we performed this meta-analysis by a comprehensive literature search via databases of PubMed, Embase, Web of Science and CNKI, updated till January 2019. Multivariate-adjusted odds ratios (ORs) and 95% confidence intervals (CIs) were extracted from eligible studies if available, to assess the relationship strengths. A total of seven eligible studies were included, comprising 4294 cancer patients (smokers: 1744 [40.6%]) and 4259 controls (smokers: 1418 [33.3%]). Results indicated a significant association of ATM rs189037 with cancer risk. In non-smokers, compared with GG genotype, AA genotype increased a 1.40-fold risk of overall cancer (OR = 1.40, 95% CI = 1.15–1.70, P(heterogeneity)=0.433, I(2) = 0.0%). Subgroup analysis in lung cancer (LC) also exhibited a significant result (OR = 1.41, 95% CI = 1.15–1.73, P(heterogeneity)=0.306, I(2) = 17.0%) only in non-smokers. However, the association was not observed in smokers, no matter for overall cancer or for LC. Our findings highlight that ATM rs189037 significantly increases cancer susceptibility in non-smokers, rather than in smokers. The association is prominent in LC. Portland Press Ltd. 2019-06-28 /pmc/articles/PMC6597848/ /pubmed/31201228 http://dx.doi.org/10.1042/BSR20191298 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Articles He, Xiaoxia Wang, Peng Li, Ying Shen, Na ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis |
title |
ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis |
title_full |
ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis |
title_fullStr |
ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis |
title_full_unstemmed |
ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis |
title_short |
ATM rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis |
title_sort | atm rs189037 significantly increases the risk of cancer in non-smokers rather than smokers: an updated meta-analysis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6597848/ https://www.ncbi.nlm.nih.gov/pubmed/31201228 http://dx.doi.org/10.1042/BSR20191298 |
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