Ataxia Telangiectasia-Mutated ()Polymorphisms and Risk of Lung Cancer in a Chinese Population.

Front Public Health

Department of Epidemiology and Environmental Health, School of Public Health and Health Professions, State University of New York (SUNY) at Buffalo, Buffalo, NY, United States.

Published: June 2017

Background: The ataxia telangiectasia-mutated () gene has a key role in DNA repair including activation and stabilization of , which implicates the importance of polymorphisms in the development of cancer. This study aims to investigate the association of two single-nucleotide polymorphisms (SNPs) with lung cancer, as well as their potential interaction with gene and other known risk factors of lung cancer.

Methods: A population-based case-control study was conducted in Taiyuan city, China with 399 cases and 466 controls matched on the distribution of age and sex of cases. The two gene SNPs, rs227060 and rs228589 as well as gene SNP, rs1042522 were genotyped using Sequenom platform. Unconditional logistic regression models were used to estimate crude and adjusted odds ratios (aOR) and 95% confidence intervals (CIs). Adjusted models controlled for age, sex, and smoking status.

Results: The study showed that TT genotype of rs227060 (aOR = 1.58, 95% CI: 1.06-2.35) and AA genotype of rs228589 were significantly associated with lung cancer (aOR = 1.50, 95% CI: 1.08-2.08) in a recessive model. Additionally, carrying variant genotypes of rs227060 (TT), rs228589 (AA), and rs1042522 (CC) concomitantly was associated with much higher risk (aOR = 3.68, 95% CI: 1.43-9.45) of lung cancer than carrying variant genotypes of any one of the above three SNPs. We also found multiplicative and additive interaction between tea drinking and rs227060 in association with lung cancer.

Conclusion: This study indicates that gene variants might be associated with development of lung cancer in Chinese population. These results need to be validated in larger and different population samples.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5462911PMC
http://dx.doi.org/10.3389/fpubh.2017.00102DOI Listing

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