XRCC1 gene polymorphisms and lung cancer susceptibility: a meta-analysis of 44 case-control studies

被引:41
作者
Dai, Liping [1 ,2 ,3 ]
Duan, Fujiao [1 ,2 ,3 ]
Wang, Peng [1 ,2 ,3 ]
Song, Chunhua [1 ,2 ,3 ]
Wang, Kaijuan [1 ,2 ,3 ]
Zhang, Jianying [1 ,2 ,3 ]
机构
[1] Zhengzhou Univ, Coll Publ Hlth, Dept Epidemiol & Biostat, Zhengzhou 450001, Peoples R China
[2] Key Lab Tumor Epidemiol, Zhengzhou 450052, Peoples R China
[3] Zhengzhou Univ, Prote Res Ctr, Zhengzhou 450052, Peoples R China
基金
中国国家自然科学基金;
关键词
Lung cancer; Polymorphism; XRCC1; Meta-analysis; BASE-EXCISION-REPAIR; DNA-REPAIR; INCREASED RISK; T-77C POLYMORPHISM; AFRICAN-AMERICANS; TOBACCO SMOKING; VARIANTS; DAMAGE; APEX1; SENSITIVITY;
D O I
10.1007/s11033-012-1818-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
X-ray repair cross-complementing group 1 gene (XRCC1) has been implicated in risk for lung cancer. However, the results from different studies remain controversial. In this meta-analysis, we have assessed 44 published case-control studies regarding associations of lung cancer risk with three common polymorphisms, codon 194, codon 280 and codon 399, and -77 T > C in the promoter region of XRCC1. The results in total population showed that the risk for lung cancer was increased among the variant homozygote Trp/Trp of codon 194 polymorphism, compared with the wild type Arg/Arg (OR: 1.19; 95 % CI 1.01-1.39), and the variant genotype CC of -77 T > C polymorphism showed a significantly increased risk of developing lung cancer, compared to wild-type genotype TT (OR: 1.91; 95 % CI 1.24-2.94). However, no associations were found between lung cancer risk and codon 280, codon 399. In the subgroup analyses by ethnicity, the OR for the variant homozygote Trp/Trp of codon 194 was 1.21(95 % CI 1.02-1.43) for Asian. When stratified by source of control, we found a protective effect of codon 194 Arg/Trp genotype (OR: 0.87; 95 % CI 0.77-0.98) and risk effect of codon 399 combined Arg/Gln + Gln/Gln variant genotype (OR: 1.09; 95 % CI 1.01-1.18) for lung cancer on the basis of hospital control. Subgroup analyses by histological types of lung cancer indicated that the heterozygote Arg/Trp in codon 194 could decrease and the combined variant genotype Arg/Gln + Gln/Gln in codon 399 could increase the risk of non-small cell lung cancer (OR: 0.69; 95 % CI 0.57-0.85 and OR: 1.14; 95 % CI 1.04-1.24). In conclusion, this meta-analysis has demonstrated that codon 194, codon 399 and -77 T > C polymorphisms of XRCC1 gene might have contributed to individual susceptibility to lung cancer. To further evaluate effect of XRCC1 polymorphisms, gene-gene interaction and gene-environment interaction on lung cancer risk, a single large sample size study with thousands of subjects is required to get conclusive results.
引用
收藏
页码:9535 / 9547
页数:13
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