Polymorphisms in base-excision repair and nucleotide-excision repair genes in relation to lung cancer risk

被引:180
作者
De Ruyck, Kim
Szaumkessel, Marcin
De Rudder, Isabelle
Dehoorne, Annelore
Vral, Anne
Claes, Kathleen
Velghe, Anj A.
Van Meerbeeck, Jan
Thierens, Hubert
机构
[1] Univ Ghent, Dept Anat Embryol Histol & Med Phys, B-9000 Ghent, Belgium
[2] State Univ Ghent Hosp, Dept Resp Med, B-9000 Ghent, Belgium
[3] State Univ Ghent Hosp, Ctr Genet Med, B-9000 Ghent, Belgium
[4] State Univ Ghent Hosp, Dept Geriatr, B-9000 Ghent, Belgium
关键词
lung cancer; polymorphisms; DNA repair; smoking;
D O I
10.1016/j.mrgentox.2007.03.010
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Polymorphisms in DNA repair genes may be associated with differences in DNA repair capacity, thereby influencing the individual susceptibility to smoking-related cancer. We investigated the association of 10 base-excision and nucleotide-excision repair gene polymorphisms (XRCCI-77 T/C, Arg 194Trp, Arg28OHis and Arg399Gln; APEI Aspl48Glu; OGG1 Ser326Cys; XPA-4 G/A; XPC PAT: XPD Asp312Asn and Lys75 I Gln) with lung cancer risk in Caucasians. Genotypes were determined by PCR-RFLP and PCR-single base extension assays in 110 lung cancer patients and 110 age- and sex-matched controls, and the results were analyzed using logistic regression adjusted for relevant covariates. A significant association between the APE1 Asp 148Glu polymorphism and lung cancer risk was found, with adjusted odds ratios (OR) of 3.38 (p = 0.001) for the Asp/Glu genotype and 2.39 (P = 0.038) for the Glu/Glu genotype. Gene-smoking interaction analyses revealed a statistically significant interaction between cumulative cigarette smoking and the XRCCl Arg399Gln and XPD Lys75 I Gln polymorphisms: these polymorphisms were significantly associated with lung cancer in nonsmokers and light smokers (< 25 PY, OR = 4.92, p = 0.021 for XRCCl 399 Gln/Gln; OR = 3.62, p = 0.049 for XPD 751 Gln/Gln), but not in heavy smokers (>= 25 PY; OR = 0.68, p = 0.566 for XRCCl 399 GWGln; OR = 0.46, p = 0.295 for XPD 751 Gln/Gln). Both the XRCCl Arg 194Trp and Arg28OHis as well as the OGG1 Ser326Cys heterozygous genotypes were associated with a significantly reduced risk for lung cancer (OR = 0.32, p = 0.024; OR = 0.25, p = 0.028; OR = 0.51, p = 0.033, respectively). No associations with lung cancer risk were found for the XRCCl-77 T/C, the XPA -4 G/A and the XPC PAT polymorphisms. In conclusion, the APEI Aspl48Glu polymorphism is highly predictive for lung cancer, and cumulative cigarette smoking modifies the associations between the XRCCl Arg399Gln and the XPD Lys75 I Gln polymorphisms and lung cancer risk. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:101 / 110
页数:10
相关论文
共 46 条
[1]   Are genetic polymorphisms in OGG1, XRCC1 and XRCC3 genes predictive for the DNA strand break repair phenotype and genotoxicity in workers exposed to low dose ionising radiations? [J].
Aka, P ;
Mateuca, R ;
Buchet, JP ;
Thierens, H ;
Kirsch-Volders, M .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2004, 556 (1-2) :169-181
[2]   Functional characterization of Polymorphisms in DNA repair genes using cytogenetic challenge assays [J].
Au, WW ;
Salama, SA ;
Sierra-Torres, CH .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2003, 111 (15) :1843-1850
[3]   Genetic polymorphisms in DNA repair genes and risk of lung cancer [J].
Butkiewicz, D ;
Rusin, M ;
Enewold, L ;
Shields, PG ;
Chorazy, M ;
Harris, CC .
CARCINOGENESIS, 2001, 22 (04) :593-597
[4]   Genetic polymorphism of XRCC1 and lung cancer risk among African-Americans and Caucasians [J].
David-Beabes, GL ;
London, SJ .
LUNG CANCER, 2001, 34 (03) :333-339
[5]  
David-Beabes GL, 2001, CANCER EPIDEM BIOMAR, V10, P911
[6]   Functional characterization of Ape1 variants identified in the human population [J].
Hadi, MZ ;
Coleman, MA ;
Fidelis, K ;
Mohrenweiser, HW ;
Wilson, DM .
NUCLEIC ACIDS RESEARCH, 2000, 28 (20) :3871-3879
[7]   A novel T-77C polymorphism in DNA repair gene XRCC1 contributes to diminished promoter activity and increased risk of non-small cell lung cancer [J].
Hao, B. ;
Miao, X. ;
Li, Y. ;
Zhang, X. ;
Sun, T. ;
Liang, G. ;
Zhao, Y. ;
Zhou, Y. ;
Wang, H. ;
Chen, X. ;
Zhang, L. ;
Tan, W. ;
Wei, Q. ;
Lin, D. ;
He, F. .
ONCOGENE, 2006, 25 (25) :3613-3620
[8]   Genome maintenance mechanisms for preventing cancer [J].
Hoeijmakers, JHJ .
NATURE, 2001, 411 (6835) :366-374
[9]   The XPD variant alleles are associated with increased aromatic DNA adduct level and lung cancer risk [J].
Hou, SM ;
Fält, S ;
Angelini, S ;
Yang, K ;
Nyberg, F ;
Lambert, B ;
Hemminki, K .
CARCINOGENESIS, 2002, 23 (04) :599-603
[10]   Amino acid substitution variants of APE1 and XRCC1 genes associated with ionizing radiation sensitivity [J].
Hu, JJ ;
Smith, TR ;
Miller, MS ;
Mohrenweiser, HW ;
Golden, A ;
Case, LD .
CARCINOGENESIS, 2001, 22 (06) :917-922