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ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis

BACKGROUND: Rs189037 (G > A) is a functional single nucleotide polymorphism (SNP) in the Ataxia-telangiectasia mutated (ATM) gene that may be associated with the risk of cancer. We performed a meta-analysis to determine whether rs189037 polymorphism influences the occurrence of cancer and examine...

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Autores principales: Zhao, Zhi-liang, Xia, Lu, Zhao, Cong, Yao, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359756/
https://www.ncbi.nlm.nih.gov/pubmed/30709340
http://dx.doi.org/10.1186/s12881-019-0760-8
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author Zhao, Zhi-liang
Xia, Lu
Zhao, Cong
Yao, Jun
author_facet Zhao, Zhi-liang
Xia, Lu
Zhao, Cong
Yao, Jun
author_sort Zhao, Zhi-liang
collection PubMed
description BACKGROUND: Rs189037 (G > A) is a functional single nucleotide polymorphism (SNP) in the Ataxia-telangiectasia mutated (ATM) gene that may be associated with the risk of cancer. We performed a meta-analysis to determine whether rs189037 polymorphism influences the occurrence of cancer and examined the relationship between this SNP and the etiology of cancer. METHODS: Case-control studies were retrieved from literature databases in accordance with established inclusion criteria. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the strength of the association between rs189037 and cancer. Subgroup analysis and sensitivity analysis also were performed. RESULTS: After inclusion criteria were met, fifteen studies—comprising 8660 patients with cancer (cases) and 9259 controls—were included in this meta-analysis. Summary results indicated that an association was found between rs189037 and cancer risk. In the dominant model, the pooled OR using a random effects model was 1.207 (95% CI, 1.090–1.337; P < 0.001). The A allele of rs189037 increased the risk of lung cancer, breast cancer, and oral cancer. Results of subgroup analysis by ethnicity indicated that the SNP was associated with the risk of cancer among East Asian and Latino, but not Caucasian. CONCLUSIONS: Results of this meta-analysis suggest that rs189037 is associated with the occurrence of lung cancer, breast cancer, and oral cancer as the risk factor. These data provide possible avenues for future case-control studies related to cancer.
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spelling pubmed-63597562019-02-07 ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis Zhao, Zhi-liang Xia, Lu Zhao, Cong Yao, Jun BMC Med Genet Research Article BACKGROUND: Rs189037 (G > A) is a functional single nucleotide polymorphism (SNP) in the Ataxia-telangiectasia mutated (ATM) gene that may be associated with the risk of cancer. We performed a meta-analysis to determine whether rs189037 polymorphism influences the occurrence of cancer and examined the relationship between this SNP and the etiology of cancer. METHODS: Case-control studies were retrieved from literature databases in accordance with established inclusion criteria. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the strength of the association between rs189037 and cancer. Subgroup analysis and sensitivity analysis also were performed. RESULTS: After inclusion criteria were met, fifteen studies—comprising 8660 patients with cancer (cases) and 9259 controls—were included in this meta-analysis. Summary results indicated that an association was found between rs189037 and cancer risk. In the dominant model, the pooled OR using a random effects model was 1.207 (95% CI, 1.090–1.337; P < 0.001). The A allele of rs189037 increased the risk of lung cancer, breast cancer, and oral cancer. Results of subgroup analysis by ethnicity indicated that the SNP was associated with the risk of cancer among East Asian and Latino, but not Caucasian. CONCLUSIONS: Results of this meta-analysis suggest that rs189037 is associated with the occurrence of lung cancer, breast cancer, and oral cancer as the risk factor. These data provide possible avenues for future case-control studies related to cancer. BioMed Central 2019-02-01 /pmc/articles/PMC6359756/ /pubmed/30709340 http://dx.doi.org/10.1186/s12881-019-0760-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhao, Zhi-liang
Xia, Lu
Zhao, Cong
Yao, Jun
ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis
title ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis
title_full ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis
title_fullStr ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis
title_full_unstemmed ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis
title_short ATM rs189037 (G > A) polymorphism increased the risk of cancer: an updated meta-analysis
title_sort atm rs189037 (g > a) polymorphism increased the risk of cancer: an updated meta-analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359756/
https://www.ncbi.nlm.nih.gov/pubmed/30709340
http://dx.doi.org/10.1186/s12881-019-0760-8
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