Association of genetic polymorphisms CYP2A6*2 rs1801272 and CYP2A6*9 rs28399433 with tobacco-induced lung Cancer: case-control study in an Egyptian population

Background Several studies have reported the role of CYP2A6 genetic polymorphisms in smoking and lung cancer risk with some contradictory results in different populations. The purpose of the current study is to assess the contribution of the CYP2A6*2 rs1801272 and CYP2A6*9 rs28399433 gene polymorphisms and tobacco smoking in the risk of lung cancer in an Egyptian population. Methods A case-control study was conducted on 150 lung cancer cases and 150 controls. All subjects were subjected to blood sampling for Extraction of genomic DNA and Genotyping of the CYP2A6 gene SNPs (CYP2A6*2 (1799 T > A) rs1801272 and CYP2A6*9 (− 48 T > G) rs28399433 by Real time PCR. Results AC and CC genotypes were detected in CYP2A6*9; and AT genotype in CYP2A6*2. The frequency of CYP2A6*2 and CYP2A6*9 were 0.7% and 3.7% respectively in the studied Egyptian population. All cancer cases with slow metabolizer variants were NSCLC. Non-smokers represented 71.4% of the CYP2A6 variants. There was no statistical significant association between risk of lung cancer, smoking habits, heaviness of smoking and the different polymorphisms of CYP2A6 genotypes. Conclusion The frequency of slow metabolizers CYP2A6*2 and CYP2A6*9 are poor in the studied Egyptian population. Our findings did not suggest any association between CYP2A6 genotypes and risk of lung cancer.


Background
Lung Cancer is the most common cancer worldwide in term of new cases (1.8 million, 12.9%) & in term of death (1.6 million death, 19.4%) [1]. Cytochrome P450 2A6 (CYP2A6), one of the forms of CYP expressed in the human respiratory tract, is the main enzyme involved in the metabolic activation of tobacco-specific nitrosamines to their carcinogenic forms [2]. CYP2A6 inactivates nicotine, the principle component in cigarette smoke, to cotinine [3]. Thus it is reasonable to hypothesize that CYP2A6 activity may be related to the susceptibility of developing lung cancer among smokers.
The CYP2A6*2 variant, appears to be one of the causal polymorphisms associated with decreased or virtually absent nicotine metabolism in Caucasians [13,14]. In East and Southeast Asian populations such as Chinese, Korean, Japanese, Malaysian and Thai, CYP2A6*2 is non-existent [15][16][17][18][19]. CYP2A6*4C is the most widely studied allele in all populations. East Asian populations such as Japanese, Chinese, Korean & malysian showed the highest frequency among populations (4.9-25.6%) [2,12,17,20]. Caucasians had a frequency lower than 3% while Middle East populations such as Turkish and Iranian showed a lower frequency [21].CYP2A6*7 has a higher frequency in East and Southeast Asian populations [6,17,19,22]. On the other hand, in Indian, African, Canadian native this allele isn't found. It has also been reported in a lower frequency in Caucasian (≤0.3%) [21].
The CYP2A6*9 is present in all ethnic groups but its frequency varies from 6 to 8% in Europeans & Africans to 21% in Asian populations [23,24]. Middle East population as Turkish [10] & Iranian [25] also showed a high frequency. CYP2A6*9 was reported as one of the most common variants of CYP2A6 in Caucasians that modifies the levels of enzyme expression [10].
Considerable studies have reported the role of CYP2A6 genetic polymorphisms in lung cancer risk with some contradictory results in different populations from ethnic variation [2,[26][27][28][29][30]. It seemed probable that genetic polymorphism in CYP2A6 causing a lack of or reduced activity might result in lowering tobacco-induced lung cancer risk, by decreased smoking. This is due to decreased activation of carcinogens such as nitrosamines present in tobacco smoke, or by lower nicotine catabolism or by both [2,6].
Thus knowing that CYP2A6 activity affects genetic suscebility to tobacco-induced lung cancer, individuals possessing the CYP2A6*2 and/or CYP2A6*9, but not the CYP2A6*1A allele would be expected to be at lower risk for lung cancer.
We conducted a case-control study to assess the contribution of the CYP2A6*2 rs1801272 and CYP2A6*9 rs28399433 gene polymorphisms and tobacco smoking in the risk of lung cancer in an Egyptian population.

Subjects
This study was a collaboration between National Research Center and National Cancer Institute (NCI) Cairo University. A case-control study was conducted that included 150 unrelated adult patients with primary lung cancer and 150 unrelated controls. The case series consisted of patients presented to NCI details of which have been described elsewhere [31]. Almost half of the patients seen at NCI-Cairo came from the Cairo metropolitan area, whereas the rest of the patients were from other regions in South and North Egypt. Patients from the non-Cairo regions sought management at NCI-Cairo because it has the largest lung cancer services in Egypt for surgical and medical oncology & radiotherapy. All subjects included in the study were interviewed to fulfill questionnaire covering demographic information, data on smoking, occupational history and family history of malignancy. All subjects were aware of the study protocol and gave written informed consent. The study was approved by the ethical committee of the National Research Center.

DNA extraction
A peripheral blood sample is obtained from each subject through venipuncture. Blood was collected in tubes with EDETA. Extraction of genomic DNA was performed using a QIAamp DNA extraction kit according to the manufacturer's protocol.

Selecting SNPs
We searched relevant publications from 1990 to 2013 in the National Center for Biotechnology Information (NCBI) data base using the following keywords: "CYP2A6", "cigarette smoking", "lung cancer" and "genetics". Based on publication in Caucasian, African and Asian populations, we expect that: CYP2A6*2 and CYP2A6*9 would be interesting because the kinetics of nicotine metabolism are altered in individuals carrying any or both of these alleles.
Genotyping of CYP2A6 gene CYP2A6*2 and CYP2A6*9 polymorphisms were genotyped using TaqMan® SNP Genotyping Assays. Primers and probes were designed by Applied Biosystems (Foster City, CA, USA) and analyses were performed on ABI 7500 Real Time PCR system (Applied Biosystems) according to the manufacturer's protocol.
For CYP2A6*2 (1799 T > A) [rs1801272; assay ID: C_ 27861808_60], the VIC/FAM sequence was as follows: For CYP2A6*9 (− 48 T > G) [rs28399433; assay ID: C_ 30634332_10], the VIC/FAM sequence was as follows: For genotyping quality control, negative controls were included in all SNPs and 10% of samples were randomly selected and analyzed in duplicates and the concordance rate was 100%.

Statistical analysis
Data were analyzed using SPSS version 18.0 (Chicago, IL, USA). Data were expressed as number and percentages of total for categorical variables. The Chisquare test (χ 2 ) was used to compare the distribution of CYP2A6 genotypes between the groups. Likelihood ratio was used when the expected count was less than 5 in more than 20% of the cells. The associations between genotype and risk of lung cancer were estimated by odds ratio (OR) and 95% confidence interval (95% CI) using logistic regression models. The ORs were adjusted for age, smoking status, and pack-years. P-value < 0.05 was considered significant. Table 1 presents the baseline characteristics of 150 lung cancer cases and 150 controls. There were statistically significant differences between age & gender. The mean age of patients is (56.7 ± 9.79 years) and that of controls is (43.3 ± 11.1 years) (p < 0.001), denoting that older age is associated with higher risk of lung cancer. A statistically significant gender difference was found between the 2 groups; 48.7% males and 51.3% females in controls and 76% males and 24% females in cancer cases, (X 2 = 25.82, P < 0.0001) with increased males risk to develop lung cancers than females.

Results
Smoking was significantly higher among cancer cases (62% smokers) compared to control (20% smokers), P < 0.0001, and (OR = 2.78, CI: 2.0-3.86) denoting a higher risk to develop lung cancer in smokers by 2.78 times the non-smokers, independent of the heaviness of smoking.
Two genotypes were detected in CYP2A6*9; heterozygote AC and homozygote CC. AC genotype was found in 4 cases in control group; 3 males and 1 female, all cases were non-smokers and 6 cases in lung cancer group; 4 males and 2 females from which 2 males were smokers > 20 pack-year. All cases were diagnosed as NSCLC (2 adenocarcinoma, 1 squamous and 3 others). CC genotype was found in 1 control case, a male, smoking > 20 pack-year (Fig. 1). One heterozygous genotype was detected in CYP2A6*2; AT. It was found in one case of lung cancer; a non-smoker male diagnosed as adenocarcinoma (Fig. 2). The 2 polymorphisms CYP2A6*9 AC  and CYP2A6*2 AT were detected in a non-smoker female control case. There was no statistical difference between the Wild type CYP2A6*1AA and CYP2A6*9, CYP2A6*2 polymorphisms regarding age, sex, smoking status, pack-year (Table 2). There was no statistical significant association between risk of lung cancer, smoking habits, heaviness of smoking and the different polymorphisms of CYP2A6 genotypes (Table 3).
There was no statistical significant difference in the CYP2A6 genotypes in different stages of lung cancer (Table 4).

Discussion
CYP2A6 has been proposed as a novel target for smoking cessation because of its major contribution to nicotine metabolism. To the best of our knowledge this is the first study to address the relationship between CYP2A6 status, smoking & lung cancer in an Egyptian population. Our data are valuable because cases that presented to NCI were from different governorates of Egypt. The CYP2A6*1A allele is considered the wild type, corresponding to normal enzymatic activity [16]. Based on reports in the literature, we expect that CYP2A6*2 & CYP2A6*9 would be intresting because they code for reduced activity. Many human nicotine pharmacokinetic & CYP2A6 studies have demonstrated the contribution of multiple decrease-, increase-, and loss-of-function polymorphisms in CYP2A6 to the variability in nicotine metabolism [23]. In our study the control group was sampled at random thus their age  distribution was much younger than that of lung cancer cases. This explains the statistical significant difference in age between cases and control. Age isn't a confounder in our study and isn't intended to be examined in the analysis of CYP2A6 polymorphism. The tested polymorphisms are not affected by age and our aim was to to assess the contribution of the CYP2A6*2 and CYP2A6*9 gene polymorphisms and tobacco smoking in the risk of lung cancer.

Frequency and ethnic variation
Our results showed that the frequency of CYP2A6*2 and CYP2A6*9 were 0.7% and 3.7% respectively. There was no statististical significant difference in the frequency of the tested variants between control and lung cancer goups. Further statistical studies were difficult due to low frequency of variants. Neverthelss, these poor frequencies were reported in other studies. In African populations (Afro American & Ethiopian), the CYP2A6*2 frequency is less than 1% [16,17,19] while it was found to be one of the major variant alleles in Caucasians; with frequency 1-3% [17,19]. The frequency of CYP2A6*2, and *9 detected in a Brazilian population was 1.7, and 5.7% respectively [32] while in Turkish population the CYP2A6* 2 is not existing [33]. Recent researches that had analysed different frequencies of CYP2A6 genetic variants in different ethnic groups; found that the frequency of CYP2A6*2, and *9 in Caucasian almost double our findings in the Egyptian population [23]. The frequencies of CYP2A6 *2 allele in different ethenic population were 1.1%, 0.0%, 2.2%, 0.0%, 0.0% and those of CYP2A6*9 were 7.1%, 15.5%, 7.1%, 15.6%, 20.3% in African American, Canadian, Caucasian, Chinese and Japanese respectively [9,10,12,18,19,[34][35][36].
Little is known about the genetic factors contributing to smoking in Egyptians. In the present study, although no statistical difference were found between CYP2A6 variants and smoking status, most cases with CYP2A6 polymorphisms were non-smoker, 10 cases from 13; 100% and 81.8% non-smokers in CYP2A6*2 and CYP2A6*9 respectively compared to 58% in CYP2A6*1 indicating a role of CYP2A6 gene variants in affecting smoking status, with slow metabolizers smoking less than fast metabolizers. Verde & colleagues [41], found that CYP2A6*2 polymorphism was strongly linked to smoking status. Moreover, it was found that the amounts of cigarette consumed daily by individuals, who harbored CYP2A6*9, were significantly less than that consumed by those who carried CYP2A6*1 (P = 0.01) [6]. Slow metabolizers (as determined by CYP2A6*2, *4, *9 and *12 alleles), are very unlikely to be smokers, take smaller puff volumes and smoke fewer cigarettes per day. They also have lower levels of dependence, benefit more from nicotine patch replacement therapy and are more capable to quit compared to normal metabolizers [2,16,19,38,[42][43][44][45][46][47][48].
Contrastingly two different meta-analyses failed to confirm any evidence of the association between the CYP2A6 diminished-activity polymorphisms and cigarette consumption. The investigators of both concluded that there is no association between the reduced-activity CYP2A6 alleles and the number of cigarettes smoked [49,50].
Malaiyandi & colleagues [16] have postulated that the continued effect of slow metabolism on reducing the number of cigarette smoked, allthrough the smoking history of slow inactivators, may influence withdrawal mechanisms and consequently aids quitting among these individuals. The noticeable temporal effect of CYP2A6 on smoking behavior and nicotine dependence necessitates further research. The poor frequencies of the variant alleles of slow inactivators extend our understanding of the impact of CYP2A6 genotype on smoking risk and behavior in Egyptian  According to the study by Loffredo & colleagues [52], the national prevalence of former cigarette smoking among males was 18.1%, and 27.5% reported current smoking.

Lung cancer
Sqamous cell carcinoma and Small cell lung cancer (SCLC) are major types of lung cancer caused by smoking, while adenocarcinoma isn't regarded as a common histological type in smokers [53,54]. In the present study, all lung cancer cases (6), with CYP2A6*2 and *9 polymorphisms were diagnosed as NSCLC, 3 of them were adenocarcinoma. Statistical interpretations could not be done due to the low frequency of variants in the study. A former study [29], did not find a significant association between this CYP2A6 polymorphism and risk of adenocarcinoma or other histological types of lung cancer. Studies of CYP2A6 inhibition demonstrated a role for the enzyme in the occurrence of lung cancer and hence have directed the interest in CYP2A6 as a target for cancer prevention [28,55]. Investigating the role of CYP2A6 genotype in effective programs implemented for lung cancer screening may improve cancer risk prediction and assist selecting individuals who could benefit from preventative measures whether behavioural or pharmacological [56]. Ariyoshi & colleagues [2], demonstrated that individuals homozygous for the CYP2A6*1A allele (*1A/*1A) have the highest risk for tobacco-related lung cancer in Japanese male smokers. They also concluded that due to higher prevelence of the functionally active CYP2A6 gene in Caucasians compared to Asians, the genetic polymorphism of CYP2A6 may be a factor justifying the interindividual difference in predisposition to lung cancer among smokers. Consistent to the previous concept Benowitz et al. [57] concluded that the slower nicotine metabolism and therefore lower nicotine uptake per cigarette may explain lower incidence of lung cancer in Asians compared to Caucasians. In the present study we failed to find a significant association between CYP2A6 genotypes and risk of lung cancer. Our data is similar to the study by London & colleagues [39] who reported no significant relationship between the CYP2A6 inactive allele, mainly concentrating on the CYP2A6*2, and lung cancer risk.
Discordant results have been demonstrated on the association of CYP2A6 genetic polymorphisms and lung cancer risk [2,26,27,29,39,58]. These contradictory results seem to be caused by the too small frequencies of the inactive alleles such as CYP2A6*2 and CYP2A6*4 in some studies to find a possible relationship with adequate statistical power [26,29]. The protecting effect of CYP2A6 slow metabolism on lung cancer risk is more obvious in populations including subjects common to harbour CYP2A6 non-functional alleles as the Japanese compared to Caucasian & other populations who include individuals harbouring low frequency of CYP2A6 slow metabolizers. It is unclear whether the risk for lung cancer is mediated through the effect on smoking behavior or whether it also involves increased sensitivity to carcinogens present in cigarette smoke [59]. Liu & colleagues [60] suggested that decreasing or abolishing the activity of the CYP2A6 by means of specific inhibitors might prevent the frequency of occurrence of tobacco-induced lung cancer in smokers only. In this study, 5 out of 7 lung cancer cases (71.4%) with CYP2A6 slow metabolizer were non-smokers.
It is worth noting that our study has some limitations. First because the number of subjects is low, significant differences in smoking behaviors were not observed between those with and without CYP2A6*2 & CYP2A6*9. Further studies with larger population samples may present more detailed results. Second, we concentrated on only CYP2A6*2 & CYP2A6*9 genetic polymorphisms. The effects of other polymorphisms of CYP2A6 on smoking habits should be examined; CYP2A6*4 and *7 are also major functional polymorphisms.

Conclusions
Our study, in the setting of patients with lung cancer demonstrates that the frequency of slow metabolizer CYP2A6*2 and CYP2A6*9 are poor in the studied Egyptian population; who are non-smokers. Our findings did not suggest any association between CYP2A6 genotypes and risk of lung cancer.
Abbreviations CI: Confidence interval; CYP2A6: Cytochrome P450 2A6; NCBI: National Center for Biotechnology Information; NCI: National Cancer Institute; NSCLC: Non small cell lung cancer; OR: Odds ratio; SCLC: Small cell lung cancer; SD: Standard deviation; SNPs: Single nucleotide polymorphisms