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

被引:4
|
作者
Myneni, Ajay A. [1 ]
Chang, Shen-Chih [2 ]
Niu, Rungui [3 ]
Liu, Li [4 ]
Zhao, Baoxing [4 ]
Shi, Jianping [4 ]
Han, Xiaoyou [3 ]
Li, Jiawei [5 ]
Su, Jia [5 ]
Yu, Shunzhang [5 ]
Zhang, Zuo-Feng [2 ]
Mu, Lina [1 ]
机构
[1] SUNY Buffalo, Dept Epidemiol & Environm Hlth, Sch Publ Hlth & Hlth Profess, Buffalo, NY 14260 USA
[2] Univ Calif Los Angeles, Dept Epidemiol, Fielding Sch Publ Hlth, Los Angeles, CA 90024 USA
[3] Shanxi Tumor Hosp, Taiyuan, Shanxi, Peoples R China
[4] Taiyuan City Ctr Dis Control & Prevent CDC, Taiyuan, Shanxi, Peoples R China
[5] Fudan Univ, Sch Publ Hlth, Shanghai, Peoples R China
关键词
lung cancer; ataxia telangiectasia-mutated gene; DNA repair; single-nucleotide polymorphisms; Chinese population; GENETIC POLYMORPHISMS; BREAST-CANCER; ASSOCIATION; P53; PHOSPHORYLATION; HAPLOTYPES; KINASES;
D O I
10.3389/fpubh.2017.00102
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: The ataxia telangiectasia-mutated (ATM) gene has a key role in DNA repair including activation and stabilization of p53, which implicates the importance of ATM polymorphisms in the development of cancer. This study aims to investigate the association of two ATM single-nucleotide polymorphisms (SNPs) with lung cancer, as well as their potential interaction with p53 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 ATM gene SNPs, ATMrs227060 and ATMrs228589 as well as p53 gene SNP, p53rs1042522 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 ATMrs227060 (aOR = 1.58, 95% CI: 1.06-2.35) and AA genotype of ATMrs228589 were significantly associated with lung cancer (aOR = 1.50, 95% CI: 1.08-2.08) in a recessive model. Additionally, carrying variant genotypes of ATMrs227060 (TT), ATMrs228589 (AA), and p53rs1042522 (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 ATMrs227060 in association with lung cancer. Conclusion: This study indicates that ATM 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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页数:8
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