The Joint Effect of hOGG1, APE1, and ADPRT Polymorphisms and Cooking Oil Fumes on the Risk of Lung Adenocarcinoma in Chinese Non-Smoking Females

Abstract

Background

The human 8-oxoguanine DNA glycosylase 1 (hOGG1), apurinic/apyrimidinic endonuclease 1 (APE1), and adenosine diphosphate ribosyl transferase (ADPRT) genes play an important role in the DNA base excision repair pathway. Single nucleotide polymorphisms (SNPs) in critical genes are suspected to be associated with the risk of lung cancer. This study aimed to identify the association between the polymorphisms of hOGG1 Ser326Cys, APE1 Asp148Glu, and ADPRT Val762Ala, and the risk of lung adenocarcinoma in the non-smoking female population, and investigated the interaction between genetic polymorphisms and environmental exposure in lung adenocarcinoma.

Methods

We performed a hospital-based case-control study, including 410 lung adenocarcinoma patients and 410 cancer-free hospital control subjects who were matched for age. Each case and control was interviewed to collect information by well-trained interviewers. A total of 10 ml of venous blood was collected for genotype testing. Three polymorphisms were analyzed by the polymerase chain reaction-restriction fragment length polymorphism technique.

Results

We found that individuals who were homozygous for the variant hOGG1 326Cys/Cys showed a significantly increased risk of lung adenocarcinoma (OR = 1.54; 95% CI: 1.01–2.36; P = 0.045). When the combined effect of variant alleles was analyzed, we found an increased OR of 1.89 (95% CI: 1.24–2.88, P = 0.003) for lung adenocarcinoma individuals with more than one homozygous variant allele. In stratified analyses, we found that the OR for the gene-environment interaction between Ser/Cys and Cys/Cys genotypes of hOGG1 codon 326 and cooking oil fumes for the risk of lung adenocarcinoma was 1.37 (95% CI: 0.77–2.44; P = 0.279) and 2.79 (95% CI: 1.50–5.18; P = 0.001), respectively.

Conclusions

The hOGG1 Ser326Cys polymorphism might be associated with the risk of lung adenocarcinoma in Chinese non-smoking females. Furthermore, there is a significant gene-environment association between cooking oil fumes and hOGG1 326 Cys/Cys genotype in lung adenocarcinoma among female non-smokers.

About the Authors:

Xiaoxia Xue

Affiliation: The Third Center of Laboratory Technology and Experimental Medicine, China Medical University, Shenyang, PR China

Zhihua Yin

Affiliation: Department of Epidemiology, School of Public Health, China Medical University, Shenyang, PR China

Yao Lu

Affiliation: The Third Center of Laboratory Technology and Experimental Medicine, China Medical University, Shenyang, PR China

Haibo Zhang

Affiliation: Department of Radiotherapy, Shenyang Northern Hospital, Shenyang, PR China

Ying Yan

Affiliation: Department of Radiotherapy, Shenyang Northern Hospital, Shenyang, PR China

Yuxia Zhao

Affiliation: Department of Radiation Oncology, First Affiliated Hospital of China Medical University, Shenyang, PR China

Xuelian Li

Affiliation: Department of Epidemiology, School of Public Health, China Medical University, Shenyang, PR China

Zeshi Cui

Affiliation: The Third Center of Laboratory Technology and Experimental Medicine, China Medical University, Shenyang, PR China

Miao Yu

Affiliation: The Third Center of Laboratory Technology and Experimental Medicine, China Medical University, Shenyang, PR China

Lu Yao

Affiliation: The Third Center of Laboratory Technology and Experimental Medicine, China Medical University, Shenyang, PR China

Baosen Zhou

* E-mail: [email protected]

Affiliation: Department of Epidemiology, School of Public Health, China Medical University, Shenyang, PR China

Introduction

Lung cancer has become a major cause of cancer mortality worldwide, especially in China, and pathological studies have found that adenocarcinoma is the main form of lung cancer in the female population [1], [2]. It is well known that smoking is the most important risk factor for lung cancer, but in the past 30 years, the incidence and death rate of lung cancer is increasing in women who have a low rate of smoking [3]–[5]. Lung cancer maybe caused mainly by the other factors in Chinese women, therefore, it is important to study the factors that affect female lung cancer, especially non-smoking females.

Environmental exposure and genetic polymorphisms might contribute to the variation in individual lung cancer risk. Recent lung cancer studies have focused on identifying effects of single nucleotide polymorphisms (SNPs) in candidate genes; in particular, DNA repair genes are being increasingly studied. DNA repair systems play a fundamental role in the maintenance of genomic integrity and protect the human genome from damage caused by environmental carcinogens. Genetic variations in DNA repair genes are thought to affect DNA repair capacity and are suggested to be associated with a risk for lung cancer [6]–[8].

As one of the DNA repair pathways, the DNA base excision repair (BER) pathway plays an important role in repairing DNA damage caused by oxidation, deamination, and alkylation, and protecting cells against the damage of endogenous and exogenous carcinogens [9]–[11]. The human 8-oxoguanine DNA glycosylase 1 (hOGG1), apurinic/apyrimidinic endonuclease 1 (APE1) and adenosine diphosphate ribosyl transferase (ADPRT) genes play an important role in the BER pathway [12]–[14]. The hOGG1 gene encodes a DNA glycosylase and completes repair by releasing the 8-oxoG base caused by DNA reactive oxygen [15]–[17]. The APE1 gene is located on chromosome 14q11.2-q12 and a rate -limiting enzyme in the BER pathway that repairs basic sites in DNA and functions as a redox activator, which regulates some transcription factors, and then participates in the BER process [18]–[20]. The ADPRT gene is located at chromosome 1q41–q42 region, plays a direct and important role in the long-path BER pathway and it can bind to single-strand breaks in DNA [21]–[23]. hOGG1 Ser326Cys, APE1 Asp148Glu and ADPRT Val762Ala are three common candidate single-nucleotide polymorphisms, and there were lots of studies investigated the association between BER SNPs and the risk of cancer [24], [25]. Recently, several studies have demonstrated the associations between these genetic polymorphisms and the risk of lung cancer, but the results vary in different ethnic populations and with different environmental exposure [26]–[33].

In the present study, we performed a case-control study to identify the association between the polymorphisms of hOGG1, APE1, and ADPRT, and the risk of lung adenocarcinoma in the non-smoking female population in Shenyang, China. We investigated the joint effects of three genes in the same pathway and the interaction between genetic polymorphisms and environmental exposure in lung adenocarcinoma.

Methods

Subjects

This hospital-based case-control study included 410 lung adenocarcinoma patients and 410 cancer-free hospital controls. All subjects were non-smoking females and they were from unrelated ethnic Han Chinese. The cases were recruited during January 2002 to January 2008 at the First Affiliated Hospital of China Medical University and Shenyang Northern Hospital. All patients were histologically confirmed to have lung adenocarcinoma before any radiotherapy and chemotherapy. During the same time, controls were selected from cancer-free patients with other lung diseases, but who were free of a history of cancer, and mainly suffered from bronchitis, pulmonary disease and emphysema. Controls were frequency-matched to case subjects for age (±5 years). This study was approved by the institutional review board of China Medical University and written informed consent was obtained from all participants.

Data Collection

A total of 10 ml of venous blood was collected from each patient. Patients were interviewed to collect information for demographics and environmental exposure by well-trained interviewers at the time they were admitted to hospital. Information included demographic characteristics, dietary habit, and family history of cancer, fuel smoke exposure, passive smoking, cooking oil fumes exposure, and occupational exposure. An individual was defined as a smoker if she had consumed a total of 100 cigarettes in her lifetime; otherwise, she was considered as a non-smoker. For exposure to cooking oil fumes, participants were asked about the frequency of cooking and types of oils.

Genotyping Methods

Genomic DNA was extracted from peripheral blood samples using the guanidine hydrochloride (GuHCl) method. Genotyping of hOGG1 Ser326Cys, APE1 Asp148Glu and ADPRT Val762Ala was performed using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. The PCR primers used were as follows: hOGG1 Ser326Cys: 5′-GTGGATTCTCATTG CCTTCG-3′ (forward) and 5′-CTGTTGCTGTCGAGACTGC-3′ (reverse); APE1 Asp148Glu: 5′-TAATTCTGTTTCATTTCTATAGGCTA-3′ (forward) and 5′-TGCA TTAGGTACATATGCTGTT-3′ (reverse); and ADPRT Val762Ala: 5′-TTTGCTCC TCCAGGCCAACG-3′ (forward) and 5′-TGGAAGTTGGGACCGCTGC-3′ (reverse). The PCR products were digested with restriction enzyme Fnu4HI (for hOGG1 Ser326Cys), FspBI (for APE1 Asp148Glu) and BstUI (for ADPRT Val762Ala) to determine the genotypes. More than 10% of the samples were randomly selected for repeat tests, and the results were 100% concordant.

Statistical Analysis

We used the Pearson’s chi square test and/or student’s t-test to compare the differences in demographic variables, environmental risk factors, and genotypes of the three genes between cases and controls. The odds ratio (OR) and 95% confidence interval (95% CI) for estimating the associations between genotypes of these genes and lung cancer were used in unconditional logistic regression analysis. The Hardy-Weinberg equilibrium was tested by performing a goodness-of-fit X2 test to compare the genotype frequencies of each SNP in the control subjects from those expected. A logistic regression model was used to evaluate gene-gene and gene-environment interactions. All data were analyzed with Statistical Product and Service Solutions (SPSS) v13.0 for Windows, if not otherwise specified. All statistical analyses were two-sided and the significance level was set at p<0.05.

Results

The basic demographic data and environmental risk factors of the 410 lung cancer patients and 410 controls are shown in Table 1. The mean ages of cases and controls (mean ± S.D.) were similar. All cases were female lung adenocarcinoma patients. We found no significant differences in age, passive smoking, family history of cancer, fuel smoke exposure, education, and monthly income between the case and control groups. However, more cases were exposed to cooking oil fumes than in the controls (OR 1.62; 95% CI: 1.21–2.18; P = 0.001).

[Figure omitted. See PDF.]

Table 1. Basic demographic data and environmental risk factor in cases and controls.

https://doi.org/10.1371/journal.pone.0071157.t001

The distribution of hOGG1, APE1 and ADPRT gene polymorphisms in cases and controls, and the adjusted ORs associated with lung adenocarcinoma are presented in Table 2. In the controls, all the genotype distributions were in agreement with the Hardy-Weinberg equilibrium (P>0.05). Using subjects with the hOGG1 Ser/Ser genotype as the reference group, homozygous carriers of the hOGG1 326Cys/Cys genotype had a 1.54-fold risk of lung adenocarcinoma compared with the homozygous wild genotypes (95% CI: 1.01–2.36, P = 0.045). No significant association was found between APE1 148Asp/Glu polymorphisms and the risk for lung adenocarcinoma (P>0.05). Distribution of ADPRT Val762Ala polymorphisms was not associated with a risk of lung adenocarcinoma (P>0.05).

[Figure omitted. See PDF.]

Table 2. Distribution of genotypes and ORs for lung adenocarcinoma cases and controls.

https://doi.org/10.1371/journal.pone.0071157.t002

The effect of the combination of hOGG1 326Cys, APE1 148Glu and ADPRT 762Ala polymorphisms on the risk of lung adenocarcinoma is shown in Table 3. The reference group was individuals who were not homozygous for at least one of the variant alleles, considering the rarity of individuals with all three alleles. When patients homozygous for two or three gene variants were combined as one group, we found an increased OR of 1.89 (95% CI: 1.24–2.88; P = 0.003) for lung adenocarcinoma individuals with more than one homozygous variant allele of hOGG1 326 Cys/Cys, APE1 148Glu/Glu and ADPRT 762Ala/Ala. However, no significant effect was found in lung adenocarcinoma individuals with one homozygous variant allele.

[Figure omitted. See PDF.]

Table 3. The combination of hOGG1 326Cys, APE1 148Glu and ADPRT 762Ala polymorphisms on lung adenocarcinoma risk in individuals homozygous for more than one variant “risk allele.”

https://doi.org/10.1371/journal.pone.0071157.t003

To evaluate the potential gene-environment interaction, the association between the polymorphisms of hOGG1 Ser326Cys and exposure to cooking oil fumes was tested in a logistic regression model. The adjusted ORs for the interaction between hOGG1 Ser326Cys and cooking oil fumes for the risk of lung adenocarcinoma are shown in Table 4. In order to see the direct joint effect of cooking oil fumes and hOGG1 Ser326Cys, which means to create a joint effect variable with 6 values according to exposure to cooking oil fumes (no/yes) and the SNP (Ser/Ser, Ser/Cys, Cys/Cys) and then compared to no exposure and ser/ser calculate ORs for the other 5 groups, we found that the ORs for the gene-environment interaction between Ser/Cys and Cys/Cys genotypes of hOGG1 codon 326 and cooking oil fumes for the risk of lung adenocarcinoma was 1.37 (95% CI: 0.77–2.44; P = 0.279) and 2.79 (95% CI: 1.50–5.18; P = 0.001), respectively. In stratified analyses by passive smoking and fuel smoke exposure, we found no statistically significant relationships between the risk of lung adenocarcinoma and the three genetic polymorphisms.

[Figure omitted. See PDF.]

Table 4. Association between hOGG1 Ser326Cys polymorphisms and risk of lung adenocarcinoma stratified by cooking oil fume exposures.

https://doi.org/10.1371/journal.pone.0071157.t004

Discussion

The incidence of lung cancer in non-smoking female population may be caused by genetic factors and other important environmental besides tobacco smoking, because of Chinese traditional cooking style. Cooking oil fumes are one of the major indoor air pollutants and are an important risk factor of lung cancer [34], [35]. However, the joint effect of these three genes and cooking oil fumes on the risk of lung adenocarcinoma in Chinese non-smoking females were not yet reported. Therefore, we investigated the association of three genetic polymorphisms (hOGG1 Ser326Cys, APE1 Asp148Glu, and ADPRT Val762Ala) in BER genes with the risk of lung adenocarcinoma, as well as the relationship of the three genetic polymorphisms with environmental factors (cooking oil fumes) in the Chinese non-smoking female population. We found a significant association between the hOGG1 326Cys/Cys genotype and lung adenocarcinoma. Homozygous carriers of the hOGG1 326Cys/Cys genotype had a 1.54-fold risk of lung adenocarcinoma compared with the homozygous wild genotypes (Table 2).

Several studies have investigated the association of hOGG1 Ser326Cys polymorphisms with lung cancer [26]–[28], [36]–[43]. Kohno et al [26] first identified hOGG1 Ser326Cys polymorphisms and found that the 326Cys protein has a low oh8G repair activity. Our recent meta-analysis of hOGG1 Ser326Cys using data from 18 studies showed that hOGG1 Ser326Cys polymorphisms might contribute to the risk of non-small cell lung cancer in the Asian population [27]. Other previous studies have shown a significant positive association between the homozygous variant Cys/Cys genotype and lung cancer development, and some of these studies focused on smokers [28], [36]–[40]. However, there have been controversial results or no association between the hOGG1 326Ser/Cys genotype and lung adenocarcinoma reported in other studies [41]–[45]. The reason for these different results between studies is not clear, but it may be because of differences in the size of the study population and differences in ethnicity.

APE1 plays a central role in base excision repair of DNA damage [46]. APE1 Asp148Glu variants are the most common APE1 polymorphisms and have been extensively studied in lung cancer; however; the results are conflicting [47]–[51]. In the current study, we found no association between APE1 Asp148Glu polymorphisms and the risk of lung adenocarcinoma among Chinese non-smoking females, which is similar to most previous studies [47]–[49]. However, an association between APE1 Asp148Glu polymorphisms and lung cancer was reported in a Japanese study [31], a Chinese study [50], and a Belgian study [51]; this might be attributed to cigarette smoking exposure. The explanation for these differences between studies is unknown, but may be due to exposure to environmental factors or joint effects with other BER genes.

ADPRT is a DNA-binding protein involved in the regulation of BER by detecting DNA strand breaks after DNA damage [52]. The association between ADPRT Val762Ala polymorphisms and lung cancer has been studied, but not extensively. A Chinese study reported that the ADPRT Ala/Ala genotype is associated with a 1.68-fold (95% CI: 1.27–2.23) increased risk with lung cancer compared with the Val/Val genotype [32]. However, no significant associations of ADPRT Val762Ala polymorphisms with lung cancer were reported in a Korean and Japanese population [33], [53]. We also did not find any significant association between ADPRT Val762Ala and the risk of lung adenocarcinoma among Chinese non-smoking females. However, the mechanisms for the effect of ADPRT Val762Ala polymorphisms on susceptibility to lung cancer remain unknown and require further investigation.

Many factors affect DNA repair activity and the risk of lung cancer, including multiple genetic variants [8]. An increasing number of studies on the joint effects of more than one variant allele were showed that complex gene-gene interactions may significantly contribute to cancer susceptibility [54], [55]. Our results suggested that a potential combined effect among homozygous genotypes of hOGG1 326 Cys/Cys, APE1 148Glu/Glu and ADPRT 762Ala/Ala significantly increased the risk of lung adenocarcinoma in the Chinese non-smoking female population. Therefore, individuals with more than one homozygous genotype may have a higher risk for lung adenocarcinoma.

Although tobacco smoking is the main cause of lung cancer, cancer is a multifactorial disease. Some studies have suggested that cooking oil fumes may be an environmental risk factor in lung cancer in women who do not smoke [56]–[60]. It is accepted that in addition to the individual contributions of genetic differences and environmental factors, interactions between the two are important in disease development [61]. To evaluate potential gene-environment associations, the interaction or joint effect of hOGG1 Ser326Cys polymorphisms and cooking oil fumes on lung cancer was examined in the previous study and evidence supports an interaction between the Cys326 hOGG1 allele and environmental exposure to ROS resulting in increased risk of cancer [62], [63]. Based on the Chinese main traditional cooking styles, including stir-frying, decoction and deep-frying, Chinese women may inhale cooking oil fumes that contain multiple potential carcinogens during prepared food. In the present study, we found that exposure to cooking oil fumes may be an environmental risk of developing lung adenocarcinoma, which is consistent with our previous study [58]–[60]. In addition, our results reflected the potential gene-environment interactions between Cys/Cys genotypes of hOGG1 codon 326 and cooking oil fumes. This finding suggests that carrying Cys/Cys genotypes of hOGG1 may increase the risk of lung adenocarcinoma when exposed to cooking oil fumes. Although the precise mechanism of how cooking oil fumes increase the risk in lung cancer is unclear, some studies have suggested that cooking oil fumes induce oxidative DNA damage, such as DNA adducts that are involved in lung carcinogenesis in female non-smokers and additionally, heated cooking oil increases the amount of 8-OHdG in human lung adenocarcinoma CL-3 cells, and it may directly or indirectly cause an accumulation of 8-OHdG [64], [65]. Therefore deletion, polymorphism and loss of heterozygosis of hOGG1 could affect the overall efficiency of oxidative base damage repair, resulting in hyper-mutation phenotypes including cancer [66]. Therefore, hOGG1 may play an important role in repairing cooking oil fume-induced DNA damage [67].

There are several limitations in the current study. First, hospital-based studies are likely to include some selection bias in the choice of controls that may not have provided a good representation of general population that alter the conclusions. Further studies with larger population-based studies are needed to reduce bias degree. Second, the statistical power of the study may be limited by the relatively small number of subjects and the number of studied SNPs, in addition, confounding factors by known and unknown risk factors could play a role in lung cancer risk and studies on the other BER genes are needed to confirm our findings in order to examine the possible relationship between BER genes polymorphisms and lung adenocarcinoma risk. Last, our study was limited to Chinese women, and the results cannot be extrapolated to other race populations. However the current study is one of the largest studies to investigate the association between BER gene polymorphisms and the risk of lung adenocarcinoma, and to evaluate the gene-gene and gene-environment interaction in the development of lung adenocarcinoma among female non-smokers. While the exact biological mechanism for the gene-environment interaction with BER gene polymorphisms is not well known, larger studies in non-smoker female populations are required in the future.

In conclusion, this hospital-based case-control study showed that hOGG1 Ser326Cys polymorphisms might be associated with the risk of lung adenocarcinoma in Chinese non-smoking females. Furthermore, there is a significant gene-environment association between cooking oil fumes and the hOGG1 Cys/Cys polymorphism on lung adenocarcinoma among female non-smokers.

Author Contributions

Conceived and designed the experiments: XX BZ. Performed the experiments: XX ZY YL HZ LY. Analyzed the data: XX XL MY. Contributed reagents/materials/analysis tools: MY YZ ZC. Wrote the paper: XX BZ.

Citation: Xue X, Yin Z, Lu Y, Zhang H, Yan Y, Zhao Y, et al. (2013) The Joint Effect of hOGG1, APE1, and ADPRT Polymorphisms and Cooking Oil Fumes on the Risk of Lung Adenocarcinoma in Chinese Non-Smoking Females. PLoS ONE 8(8): e71157. https://doi.org/10.1371/journal.pone.0071157

References

1. Ferlay J, Shin H-R, Bray F, Forman D, Mathers C, et al. (2010) Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer 127: 2893–2917.

2. Chen W, Zhang S, Zou X (2010) Estimation and projection of lung cancer incidence and mortality in China. Zhongguo Fei Ai Za Zhi 13: 488–493.

3. Belani CP, Marts S, Schiller J, Socinski MA (2007) Women and lung cancer: epidemiology, tumor biology, and emerging trends in clinical research. Lung Cancer 55: 15–23.

4. Thomas L, Doyle LA, Edelman MJ (2005) Lung cancer in women: emerging differences in epidemiology, biology, and therapy. Chest 128: 370–381.

5. Zang EA, Wynder EL (1996) Differences in lung cancer risk between men and women: examination of the evidence. J Natl Cancer Inst 88: 183–192.

6. T Xi, I M Jones, H W Mohrenweiser (2004) Many amino scid subsitution variants identified in DNA repair genes during human population screening are predicted to impact protein function. Genomicsm 83: 970–979.

7. Gackowski D, Speina E, Zielinska M, Kowalewski J, Rozalski R, et al. (2003) Products of oxidative DNA damage and repair as possible biomarkers of susceptibility to lung cancer. Cancer Res 63: 4899–4902.

8. Spitz MR, Wei Q, Dong Q, Amos CI, Wu X (2003) Genetic susceptibility to lung cancer: the role of DNA damage and repair. Cancer Epidemiol Biomarkers Pre 12: 689–698.

9. Tudek B (2007) Base excision repair modulation as a risk factor for human cancers. Mol Aspects Med 28: 258–275.

10. Kothandapani A, Sawant A, Dangeti VS, Sobol RW, Patrick SM (2013) Epistatic role of base excision repair and mismatch repair pathways in mediating cisplatin cytotoxicity. Nucleic Acids Res 12: 1–12.

11. Gossage L, Perry C, Abbotts R, Madhusudan S (2012) Base excision repair factors are promising prognostic and predictive markers in cancer. Curr Mol Pharmacol 5: 115–124.

12. Hung RJ, Hall J, Brennan P, Boffetta P (2005) Genetic polymorphisms in the base excision repair pathway and cancer risk: a HuGE review. Am. J. Epidemiol 162: 925–942.

13. Simonelli V, Mazzei F, D’Errico M, Dogliotti E (2012) Gene susceptibility to oxidative damage: from single nucleotide polymorphisms to function. Mutat Res 731: 1–13.

14. Robertson AB, Klungland A, Rognes T, Leiros I (2009) DNA repair in mam malian cells: base excision repair: the long and short of it. Cell Mol LifeSci 66: 981–993.

15. Shinmura K, Yokota J (2001) The OGG1 gene encodes a repair enzyme for oxidatively damaged DNA and is involved in human carcinogenesis. Antioxid Redox Signal 3: 597–607.

16. Weiss J, Goode E, Ladiges W, Ulrich C (2005) Polymorphic variation in hOGG1 and risk of cancer: a review of the functional and epidemiologic literature. Mol Carcinog 42: 127–141.

17. Boiteux S, Radicella JP (2000) The human OGG1 gene: structure, functions, and its implication in the process of carcinogenesis. Arch Biochem Biophys 377: 1–8.

18. Ramana CV, Boldogh I, Izumi T, Mitra S (1998) Activation of apurinic/apyrimidinic endonucleaes in human cells by reactive oxygen species and its correlation with their adaptive response to genotoxicity of free radicals. Proc Natl Acad Sci USA 95: 5061–5066.

19. Dianov GL, Sleeth KM, Dianova II, Allinson SL (2003) Repair of abasic sites in DNA. Mutat Res 531: 157–163.

20. Hadi MZ, Coleman MA, Fidrlis K, Mohrenweiser HW, Wilson 3rd (2000) Functional characterization of APE1 variants identified in the human population. Nucleic Acida Res 28: 3871–3879.

21. Wood RD, Mitchell M, Sgouros J, Lindahl T (2001) Human DNA repair genes. Science (Washington DC) 291: 1284–1289.

22. Yu SW, Wang H, Poitras MF, Coombs C, Bowers WJ, et al. (2002) Mediation of poly (ADP-ribose) polymerase-1-dependent cell death by apoptosis-inducing factor. Science 297: 259–263.

23. Lockett KL, Hall MC, Xu J (2004) The ADPRT V762A genetic variant contributes to prostate cancer susceptibility and deficient enzyme function. Cancer Res 64: 6344–6348.

24. Miao X, Zhang X, Zhang L, Guo Y, Hao B, et al. (2006) Adenosine diphosp hate ribosyl transferase and x-ray repair cross-complementing 1 polymor phisms in gastric cardia cancer. Gastroenterology 131: 420–427.

25. Liu L, Yuan P, Liu L, Wu C, Zhang X, et al. (2011) A functional -77T>C polymorph ism in XRCC1 is associated with risk of breast cancer. Breast Cancer Res Treat 125: 479–487.

26. Kohno T, Shinmura K, Tosaka M, Tani M, Kim SR, et al. (1998) Genetic polymorphisms and alternative splicing of the hOGG1 gene, that is involved in the repair of 8-hydroxyguanine in damaged DNA. Oncogenen 16: 3219–3225.

27. Guan P, Huang D, Yin Z, Zhou B (2012) Association of the hOGG1 Ser326Cys polymorphism with increased lung cancer susceptibility in Asians: a meta- analysis of 18 studies including 7592 cases and 8129 controls. Asian Pacific J Cancer Pre 12: 1067–1072.

28. Le marchand L, Donlon T, Lum Jones A, Seifried A, Wilkens LR (2002) Association of the hOGG1 Ser326Cys polymorphism with lung cancer risk. Cancer Epidemiol Biomarkers Prev 11: 409–412.

29. Misra RR, Ratnasinghe D, Tangrea JA, Virtamo J, Andersen MR, et al. (2003) Polymorphisms in the DNA repair genes XPD, XRCC1, XRCC3, and APE/ref-1, and the risk of lung cancer among male smokers in Finland. Cancer Lett 191: 171–178.

30. Chang JS, Wrensch MR, Hansen HM, Sison JD, Aldrich MC, et al. (2009) Base excision repair genes and risk of lung cancer among San Francisco Bay Area Lations and African-Americans. Carcinogenesis 30: 78–87.

31. Ito H, Matsuo K, Hamajima N, Mitsudomi T, Sugiura T, et al. (2004) Gene-environment interactions between the smoking habit and polymorphisms in the DNA repair genes, APE1 Asp148Glu and XRCC1 Arg399Glu, in Japanese lung cancer risk. Carcinagenesis 25: 1395–1401.

32. Zhang X, Miao X, Liang G, Hao B, Wang Y, et al. (2005) Polymorphisms in DNA base excision repair genes ADPRT and XRCC1 and risk of lung cancer. Cancer Res 65: 722–726.

33. Choi JE, Park SH, Jeoh HS, Kim KM, Lee GY, et al. (2003) No association between haplotypes of three variants codon 81, 284, and 762 in poly (ADP-ribose) polymerase gene and risk of primary lung cancer. Cancer Epidemiol Biomarkers Prev 12: 947–949.

34. Matullo G, Dunning AM, Guarrera S, Baynes C, Polidoro S, et al. (2006) DNA repair polymorphisms and cancer risk in non-smokers in a cohort study. Carcinogenesis 27: 997–1007.

35. Ko YC, Lee CH, Chen MJ, Huang CC, Chang WY, et al. (1997) Risk factors for primary lung cancer among non-smoking women in Taiwan. Int J Epidemiol 26: 149–155.

36. Li H, Hao X, Zhang W, Wei Q, Chen K (2008) The hOGG1 Ser326Cys polymorphisms and lung cancer risk: a meta-analysis. Cancer Epidemiol Biomarkers Pre 17: 1739–1745.

37. Liu CJ, Hsia TC, Tsai RY, Sun SS, Wang CH, et al. (2010) The joint effect of hOGG1 single nucleotide polymorphism and smoking habit on lung cancer in Taiwan. Anticancer Res 30: 4141–4146.

38. Chang C, Hsiao CF, Chang GC, Ying-Huang Ying-Huang, et al. (2009) Hsiung: Interactive effect of cigarette smoking with human 8-oxoguanine DNA N-Glycosylase 1(hOGG1) polymorphisms on the risk of lung cancer: a case-control study in Taiwan. American Journal of Epidemiology 170: 695–702.

39. Hung RJ, Brennan P, Canzian F, Szeszenia-Dabrowska N, Zaridze D, et al. (2005) Large-scale inverstigation of base excision repair genetic polymorphisms and lung cancer risk in a multicenter study. J. NatI Cancer Inst 97: 567–576.

40. Zienolddiny S, Campa D, Lind H, Ryberg D, Skaug V, et al. (2006) Polymorphisms of DNA repair genes and risk of non - small cell lung cancer. Carcinogenesis 27: 560–567.

41. Park J, Chen L, Tockman MS, Elahi A, Lazarus P (2004) The human 8-oxoguanine DNA N-glycosylase 1 (hOGG1) DNA repair enzyme and its association with lung cancer risk. Pharmacogenetics 14: 103–109.

42. Sugimura H, Kohno T, Wakai K, Naqura K, Genka K, et al. (1999) hOGG1 Ser326Cys polymorphism and lung cancer susceptibility. Cancer Epidemiol Biomarkers Prev 8: 669–674.

43. Wikman H, Risch A, Klimek F (2000) hOGG1 polymorphism and loss of heterozygosity (LOH): significance for lung cancer susceptibility in a Caucasian population. Int J Cancer 88: 932–937.

44. Sunaga N, Kohno T, Yanagitani N, Sugimura H, Kunitoh H, et al. (2002) Contribution of the NQO1 and GSTT1 polymorphisms to lung adenocarcinoma susceptibility. Cancer Epidemiol Biomarkers Prev 11: 730–738.

45. Ito H, Hamajima N, Takezaki T, Matsuso K, Tajima K, et al. (2002) A limited association of OGG1 Ser326Cys polymorphisms for adenocarcinama of the lung. J Epidemiol 12: 258–265.

46. Yoshida A, Ueda T (2003) Human AP endonuclease possesses a significant activity as major 3′–5′ exonuclease in human leukemia cells. Biochem Biophys Res Commun 310: 522–528.

47. Kiyohara C, Takayama K, Nakanishi Y (2006) Association of genetic polymorphisms in the base excision repair pathway with lung cancer risk: a meta-analysis. Lung Cancer 54: 267–283.

48. Popanda O, Schattenberg T, Phong CT, Butkiewicz D, Risch A, et al. (2004) Specific combinations of DNA repair gene variants and increased risk for non-small cell lung cancer. Carcinogenesis 25: 2433–2411.

49. Ryk C, Kumar R, Thirumaran RK, Hou SM (2006) Polymorphisms in the DNA repair genes XRCC1, APEX1, XRCC3 and NBS1, and the risk for lung cancer in never-and ever-smokers. Lung Cancer 54: 285–292.

50. Shen M, Berndt SI, Rothman N, Mumford JL, He X, et al. (2005) Polymorphisms in the DNA Base Excision Repair Genes APEX1 and XRCC1 and Lung Cancer Risk in Xuan Wei, China. Anticancer Research 25: 537–542.

51. De Ruyck K, Scaumkesske M, De Rudder I, Dehoorne A, Vral A, et al. (2007) Polymorphisms in base-excision repair and nucleotide-excision repair genes in relation to lung cancer risk. Mutation Research 631: 101–110.

52. Masutani M, Nakagama H, Sugimura T (2005) Poly (ADP-ribosyl) ation in relation to cancer and autoimmune disease. Cell Mol Life Sci 62: 769–783.

53. Sakiyama T, Kohno T, Mimaki S, Ohta T, Yanagitani N, et al. (2005) Association of amino acid substitution polymorphisms in DNA repair genes TP53, POLI, REV1 and LIG4 with lung cancer risk. Int J Cancer 114: 730–737.

54. Zhong R, Liu L, Zou L, Sheng W, Zhu B, et al. (2013) Genetic variations in the TGFβ signaling pathway, smoking and risk of colorectal cancer in a Chinese population. Carcinogenesis 34: 936–942.

55. Liu L, Wu C, Wang Y, Zhong R, Wang F, et al. (2011) Association of candidate genetic variations with gastric cardia adenocarcinoma in Chinese population: a multiple interaction analysis. Carcinogenesis 32: 336–342.

56. Gao Y, Blot W, Zheng W (1987) Lung cancer among Chinese women. Int J Cance 40: 604–609.

57. Ko Y, Cheng L, Lee C (2000) Chinese food cooking and lung cancer in women nonsmokers. Am J Epidemiol 151: 140–147.

58. Yin Z, Li M, Cui Z, He Q, Zhou B (2007) Relationship between ERCC2 polymorphism and risk of lung cancer in Chinese non-smoker. Chinese journal of Cancer Research 19: 184–188.

59. Li M, Yin Z, Guan P, Li X, Cui Z, et al. (2008) XRCC1 polymorphisms cooking oil fume and lung cancer in Chinese women nonsmokers. Lung Cancer 62: 145–151.

60. Yin Z, Su M, Li X, Li M, Ma R, et al. (2009) ERCC2, ERCC1 polymorphisms and haplotypes, cooking oil fue and lung adenocarcinama risk in Chinese non- smoking females. Journal of Experimental & Clinical Cancer Research 28: 153–160.

61. Hunter DJ (2005) Gene-environment interactions in human diseases. Nat. Rev. Genet 6: 287–298.

62. Takezaki T, Gao CM, Wu JZ, Li ZY, Wang JD, et al.. (2002) hOGG1 SER326CY S polymorphism and modification by environmental factors of stomach cancer risk in Chinese. Int. J. Cancer 99, 624–627.

63. Lan Q, Mumford JL, Shen M, Demarini DM, Bonner MR, et al. (2004) Oxidative damage-related genes AKR1C3 and OGG1 modulate risks for lung cancer due to exposure to PAH-rich coal combustion emissions. Carcinogenesis 25: 2177–2181.

64. Wen Cheng Y, Lee H (2003) Environmental exposure and lung cancer among nonsmokers: An example of Taiwanese female lung cancer. J Environ Sci Health C Environ Carcinog Ecotoxicol Rev 21: 1–28.

65. Xi ZG, Li GX, Sun YM (2003) Oxidative damage of DNA, formation of its biomarker 8-hydrooxydeoxyguanisine induced by heated cooking oil. J Environ Health 20: 259–263.

66. Thomas D, Scot AD, Barbey R, Padula M, Boiteux S (1997) Inactivation of OGG1 increases the incidence of G:C-T:A transversions in Saccharomyces cerevisiae: Evidence for endogenous oxidative damage to DNA in eukaryotic cells. Mol Gen Genet 254: 171–178.

67. Wu M, Che W, Zhang Z (2008) Enhanced sensitivity to DNA damage induced by cooking oil fumes in human OGG1 deficient cells. Environmental and Molecular Mutagen 49: 265–275.