ERCC2, ERCC1 polymorphisms and haplotypes, cooking oil fume and lung adenocarcinoma risk in Chinese non-smoking females

In China, lung cancer is currently the most common cancer among men and the second one among women and is the leading cause of cancer-related deaths for both genders. The incidence and mortality rate of lung cancer in China urban populations have reached the number one among malignant tumors. Although the incidence and death rate of lung cancer is now declining in men, the incidence and death rate in women continues to increase. So in this sense it is more important to study the impact factors of lung cancer in female population. Adenocarcinoma accounts for about 40% of all lung cancer, with a higher incidence in women. It is the most frequent subtype occurring in those who have never smoked. The epidemiologic characteristics and risk factors of lung cancer in nonsmokers are not clear. As we know, many lung cancer patients didn't have the history of smoking and a lot of smokers didn't develop lung cancer [1], suggesting that host susceptibility factors may play an important role in this disease.

Recent genetic susceptibility studies of cancer have focused on single nucleotide polymorphisms (SNPs) in candidate genes, among which DNA repair genes are increasingly studied because of their critical role in maintaining genome integrity. Excision repair cross-complimentary group 1 and group 2 (ERCC1 and ERCC2) are the important DNA repair genes, playing critical roles in nucleotide excision repair (NER) pathway which is the most important system to repair a wide variety of structurally DNA lesions, including bulky adducts, cross-links [2], oxidative DNA damage, thymidine dimmers [3]and alkylating damage [4]. The two genes are all located in chromosome 19q13.2-13.3. ERCC2 codes for an evolutionarily conserved helicase, a subunit of TFIIH complex which is essential for transcription and NER. ERCC1 protein is responsible for recognition of DNA damage and removal of the damaged nucleotides in NER. SNPs in exons of DNA repair genes may influence their protein activity, resulting in differences of individual NER and DNA repair capacity (DRC) that may affect the susceptibility of lung cancer. So we selected the common SNPs in exons of ERCC2 and ERCC1 gene and with the frequency of heterozygosity >5% in the present study. The common polymorphism of ERCC1 gene is at codon 118 (C > T substitution at exon 4, without amino acid change--Asn/Asn, rs11615). The common polymorphisms of ERCC2 gene is at codon 751 (A > C substitution at nucleotide position 35931, exon 23, Lys>Gln, rs13181) and codon 312 (G >A substitution at position 23951, exon 10, Asp>Asn, rs1799793). The polymorphisms at codon 312 and 751 have been studied extensively for their potential implication in cancer risk.

The effect of the ERCC2 and ERCC1 polymorphisms, and also of the haplotypes encompassing these two genes, on susceptibility of lung adenocarcinoma in non-smoking females has not been reported so far. In the present study, we describe a case-control study of lung adenocarcinoma in non-smoking female population in Shenyang, China, to evaluate the roles of the SNPs in ERCC1 and ERCC2 gene on risk of lung adenocarcinoma and explore the interaction between genetic polymorphism and exposure to environmental risk factors in the development of lung adenocarcinoma.

In recent years, the etiological study of lung cancer remains popular all over the world. But the results are inconsistent, and as we know besides tobacco smoking, other impact factors of lung cancer are not definitive. Cigarette smoking cannot fully explain the epidemiologic characteristics of lung cancer in Chinese women, who smoke rarely but have lung cancer relatively often. Undoubtedly non-smoking females are the ideal subjects to examine unknown, yet important environmental and genetic factors of lung cancer. And because adenocarcinoma represents the main subgroup of female lung cancer and is the most frequent subtype occurring in those who have never smoked, we studied the associations between risk for development of lung adenocarcinoma and multiple genetic polymorphisms in NER genes, as well as environmental factors among Chinese non-smoking female population.

Our previous studies found the significant associations between cooking oil fume exposure and lung cancer risk in Chinese non-smoking females [5, 8]. The similar results were suggested in the present study. Individuals with exposure to cooking oil fume had a 1.61-fold increased risk of developing lung adenocarcinoma (P = 0.009). It was reported that cooking oil fume condensates can induce DNA damage [9] and result in the increase of DNA cross-links in a certain concentration [10]. Some study showed that exposure to cooking oil fume could inhibit cell growth, increase TGFbeta1 secretion, and induce oxidative stress in lung epithelial cells [11]. There are other studies suggesting the important roles of cooking oil fume exposure in lung cancer risk among nonsmoking women [12–14].

Based on our results, 751C variant allele of ERCC2 gene may contribute to risk of lung adenocarcinoma, whereas the ERCC2 312 and ERCC1 118 polymorphisms have no significant associations with lung adenocarcinoma among non-smoking females. The three SNPs selected in this study are all in exons of NER genes, which were considered to influence the protein activity, then decrease or increase the DNA repair capacity and finally associate with risk of cancer. The SNP at amino acid 751 of ERCC2 may be important in terms of ERCC2 protein activity [15], because it locate in the interactive domain, i.e. its helicase activator, p44, inside the TFIIH complex which is essential for transcription and NER [16]. The ERCC2 751 polymorphism was associated with higher levels of chromatic aberrations [17] and DNA adducts levels in non-smokers [18]. It was reported that ERCC2 751AC/CC was significantly defective in NER [19] and had a modulating effect on DRC [20]. These results suggested that ERCC2 751 polymorphism could result in a defect in NER and deficient DRC that may be responsible for increased susceptibility of cancer. Our results show that non-smoking females carrying ERCC2 751C variant allele were at an increased risk for lung adenocarcinoma compared with those carrying AA genotype (adjusted OR = 1.64). It suggests that the polymorphism of ERCC2 codon 751 plays an important role in the development of lung adenocarcinoma in non-smoking females. Previous studies in whole population got the same results [21, 22]. However some reports found the non-correlation between the polymorphisms of ERCC2 gene and risk of lung cancer [23] or the opposite results [24]. The reason for these different conclusions is not clear now. Probably the size of the study population, the particularity of exposure to carcinogen in different populations and genetic differences of study subjects play important roles in it. In addition, the ERCC2 751 polymorphism may function through haplotype but not through genetic exon to affect protein activity. Is this appropriate for other SNPs in ERCC2 and ERCC1? The exact effects and mechanisms of these polymorphisms on lung cancer need further studies to elucidate.

As reported in previous study [25], the ERCC2 751C, 312A and ERCC1 118T alleles have been found to be in linkage disequilibrium. The exploratory haplotype analyses in the present study revealed the associations between the 751A-312G-118T and 751C-312G-118C haplotypes and the increased risk of lung adenocarcinoma in non-smoking females. The result showed that none of the analyzed haplotypes included the variant allele of ERCC2 312 polymorphism. Some European studies found that ERCC2 312 and 751 polymorphisms are closely linked and their effects are difficult to be separated. Our study indicated that ERCC2 751 polymorphism may indeed be of functional importance for lung adenocarcinoma among non-smoking female population. Because it is just a statistical estimation, further studies are required to confirm its biological validity.

Few molecular epidemiological studies of lung adenocarcinoma have been conducted thus far. This study is one of the largest studies among non-smoking female population to evaluate the correlation between NER gene polymorphisms and risk of lung adenocarcinoma, and also the gene-environment interaction in the development of lung adenocarcinoma. The strength of this study is its low rate of misclassification of outcome, as all of the cases were pathologically confirmed.

In summary, our study sheds light on the relationship between polymorphisms in the DNA repair gene ERCC2 and ERCC1 with environmental risk factors and susceptibility to lung adenocarcinoma in nonsmoking females in northeast China. Our results show that the ERCC2 751C allele or the haplotypes encompassing the variant allele are associated with risk of lung adenocarcinoma in Chinese nonsmoking female population. While the functional interpretation remains elusive, additional larger studies are needed to validate our findings.

The results of the present study indicate that ERCC2 751 polymorphism (rs13181) might be a genetic risk modifier for lung adenocarcinoma in non-smoking females in China.