Background
Lung cancer is the leading cause of cancer-related death worldwide. The incidence and mortality of lung cancer have been significantly and constantly increasing over the past two decades in Korea [
1‐
3]. According to the Korean National Cancer Registry, the age-standardized incidence rate for lung cancer of Korean population was 47.5/100,000 for men and 13.3/100,000 for women in 2007 [
2], it has become the second most common malignant tumor following gastric cancer. The reason for this increase in lung cancer has not been clearly explained. Although it is well known that cigarette smoking is the major cause of lung cancer, only 10-20% of lifetime smokers are known to develop lung cancer. Additionally, lung cancer is a multicellular and multistage process involving a number of genetic changes in oncogenes, suggesting that genetic factors may play an important role in its development [
4‐
6].
Methylenetetrahydrofolate reductase (MTHFR) is an important enzyme in folate metabolism. A common mutation of the MTHFR gene is the C to T transition at nucleotide 677, which converts alanine to valine, results in a thermo-labile enzyme with decreased activity [
7]. The heterozygote and homozygous variant of C677T were shown to have 65 and 30% of the enzyme activity, respectively [
8]. The low enzymatic activity of the MTHFR C677T genotypic variant is associated with DNA hypomethylation, which may induce genomic instability or the derepression of proto-oncogenes.
To date, several studies have shown that the MTHFR C677T polymorphism are associated with either increased [
9‐
12] or decreased [
13‐
15] risk of lung cancer, whereas others observed no association between the MTHFR C677T genotype and genetic susceptibility to lung cancer [
16‐
18]. Small sample size, various ethnic groups, diet, environment, and methodologies may be responsible for the discrepancy. Therefore, a larger single study is required to evaluate MTHFR C677T polymorphisms and the lung cancer risk in a specific population. Additionally, to our knowledge, no previous report has examined the effect of MTHFR C677T polymorphisms on the risk of lung cancer in a Korean population. In the present study, we performed a large population based case-control study involving 3938 lung cancer patients and 1700 healthy controls to evaluate whether MTHFR C677T polymorphism was associated with lung cancer risk in a Korean population. Additionally, we investigated whether MTHFR C677T plays an interactive role in the lung cancer risk in relation to histological subtypes and smoking status.
Results
The characteristics of the study population are presented in Table
1. In total, 3938 cases and 1700 controls were included in these analyses. The 3938 lung cancer cases consisted of 1523 adenocarcinomas, 1519 squamous cell carcinomas, 574 small cell carcinomas, and 322 other types, including 75 large cell cancers and 247 mixed types. The mean age of patients with lung cancer was significantly higher than the control group. A statistically significant gender difference was also found between patients with lung cancer and healthy controls; the control group had more females. The proportion of smokers in lung cancer cases was higher than in the controls.
Table 1
General characteristics of subjects
No. | 3938 | 1700 |
Age(mean ± SD)* | 64.8 ± 9.6 | 52.2 ± 14.3 |
≤65 years | 1803 (45.8) | 1308 (76.9) |
> 65 years | 2135 (54.2) | 392 (23.1) |
Gender* | | |
Male | 3128 (79.4) | 821 (48.3) |
Female | 810 (20.6) | 879 (51.7) |
Smoking status* | | |
Never | 900 (22.8) | 1000 (58.8) |
Ever | 2951 (74.9) | 655 (38.5) |
unknown | 87 (2.2) | 45 (2.6) |
Histological type
| | |
ADC | 1523 (38.7) | |
SQC | 1519 (38.6) | |
SCLC | 574 (14.6) | |
Others | 322 (8.2) | |
Table
2 shows the genotype distributions for MTHFR C677T and their ORs and 95% CIs in lung cancer. The distribution of the MTHFR C677T gene polymorphisms in the controls was calculated by the Hardy-Weinberg equilibrium. The MTHFR C677T frequencies of CC, CT, and TT genotypes were 34.5%, 48.5%, and 17.0% in lung cancer, and 31.8%, 50.7%, and 17.5% in the controls, respectively. The frequencies of combination for 677 CT heterozygous and 677 TT homozygous were observed 65.4% in lung cancer and 68.2% in the controls. Compared with the MTHFR 677 CC genotype, the TT and CT genotypes showed a protective effect for the risk of lung cancer when adjustments were made for age and gender, overall TT versus CC (OR = 0.88; 95% CI = 0.71-1.07) and overall CT versus CC (OR = 0.90; 95% CI = 0.77-1.04); however, the results did not reach statistical significance.
Table 2
Distribution of MTHFR C677T and their association with lung cancer risk
CC
| 1361 (34.5) | 540 (31.8) | 1 | |
CT
| 1909 (48.5) | 862 (50.7) | 0.90 | 0.77-1.04 |
TT
| 668 (17.0) | 298 (17.5) | 0.88 | 0.71-1.07 |
CT+TT
| 2577 (65.4) | 1160 (68.2) | 0.89 | 0.78-1.03 |
Table
3 shows subgroup analysis by gender, age and histological type for the MTHFR C677T polymorphisms. When the MTHFR 677CC genotype was used as the reference group, the MTHFR 677 CT genotype were associated with a significantly reduced risk in squamous cell carcinoma (OR = 0.78; 95% CI = 0.64- 0.96), the combined variant genotypes (677 CT + TT) also showed a protect effect on the risk of squamous cell carcinoma (OR = 0.79; 95% CI = 0.65- 0.95), while there was no significant association in other histological types of lung cancer. There were no heterogeneities among subgroups of gender (male, female), age (age ≤65, age > 65), smoking (never smoker, ever smoker), histological type (adenocarcinoma, squamous cell carcinoma, small cell carcinoma, other types). Nor did we find evidence for an interaction between the MTHFR C677T polymorphisms and age and gender or smoking habit.
Table 3
Subgroup analysis for the MTHFR C677T polymorphisms
Gender
| | | | | 0.90 | | | 0.96 |
Male | 0.89 | 0.74-1.08 | 0.90 | 0.63-1.16 | | 0.89 | 0.74-1.07 | |
Female | 0.91 | 0.72-1.16 | 0.85 | 0.63-1.16 | | 0.90 | 0.72-1.12 | |
Age
| | | | | 0.39 | | | 0.84 |
≤ 65 | 0.96 | 0.80-1.16 | 0.87 | 0.68-1.12 | | 0.94 | 0.79-1.12 | |
> 65 | 0.80 | 0.62-1.04 | 0.90 | 0.64-1.25 | | 0.83 | 0.65-1.05 | |
Smoking status
| | | | | 0.55 | | | 0.77 |
Never | 0.90 | 0.72-1.12 | 0.80 | 0.60-1.07 | | 0.87 | 0.71-1.08 | |
Ever | 0.89 | 0.73-1.10 | 0.97 | 0.73-1.28 | | 0.91 | 0.75-1.11 | |
Histological type
| | | | | 0.64 | | | 0.99 |
ADC | 0.89 | 0.75-1.05 | 0.93 | 0.74-1.16 | | 0.90 | 0.76-1.06 | |
SQC | 0.78 | 0.64-0.96 | 0.80 | 0.61-1.04 | | 0.79 | 0.65-0.95 | |
SCLC | 0.96 | 0.75-1.22 | 0.83 | 0.59-1.15 | | 0.92 | 0.73-1.17 | |
Others | 0.93 | 0.70-1.26 | 0.77 | 0.51-1.15 | | 0.89 | 0.67-1.18 | |
Discussion
The current study represents the largest sample (3938 lung cancer patients and 1700 controls) of a single population reported to evaluate a possible association between MTHFR C677T gene polymorphism and susceptibility to lung cancer. To our knowledge, this is also the first report to examine the association between MTHFR C677T polymorphisms and susceptibility to lung cancer in a Korean population. We found that the MTHFR 677 CT and TT showed weak protection for overall lung cancer, although the results were not statistically significant. However, by histological subtype, we found significant protection of the MTHFR CT genotype for squamous cell carcinoma risk.
The combination of 677 TT homozygous with 677 CT heterozygous also appeared to have a protection effect on the risk of squamous cell carcinoma. We observed no significant interactions between the MTHFR C677T polymorphism and smoking, gender, or age.
Results of several studies examining the role of the MTHFR C677T polymorphism in lung cancer susceptibility have been inconsistent. Liu et al. [
14] and Jeng et al. [
13] in Taiwan and Suzuki et al. [
15] in Japan showed that the MTHFR 677 TT genotype was associated with a decreased risk of lung cancer. However, Siemianowicz et al. [
11] in Poland, Hung et al. [
9] in Central Europe, and Shen et al. [
10] in China showed that individuals with MTHFR TT genotype had an increased risk of lung cancer versus those with the wild-type homozygous variant, while a recent meta-analysis by Mao et al. [
20] based on eight case-control study suggested no evidence for a major role of the MTHFR C677T polymorphisms in carcinogenesis of lung cancer. Small sample size, various ethnic groups, diet, environment, and methodologies might be responsible for the discrepancy.
The pathogenesis of adenocarcinoma is considered to be somewhat different from that of squamous cell carcinomas, and whether the effect of MTHFR C677T polymorphism differs by lung cancer histology remains unclear. We performed a stratification analysis by histological type, which is lacking in most previous studies, and found that the MTHFR 677 CT genotype was associated with a significantly decreased risk for lung squamous cell carcinoma (OR = 0.78, 95%CI = 0.64-0.96), supporting the potential effect of MTHFR C677T polymorphism on lung squamous cell carcinoma. In other histological type of lung cancer, such as adenocarcinoma and small cell lung cancer, we found no association between C677T MTHFR genotype and lung cancer risk. A similar result was seen in a Japanese study in which no effect of MTHFR C677T polymorphism on the risk of overall lung cancer was evident, but on histology based analysis, the MTHFR 677T allele was associated with a reduced risk of squamous/small cell carcinoma [
15]. While Siemianowicz et al. [
11] reported that the 677TT genotype was associated with a significantly higher risk of non-small cell lung cancer.
The role of MTHFR polymorphisms in modulating cancer risk is associated with folate status. Under adequate folate conditions, the protective effect of the 677TT genotype turns to a situation of elevated risk of lung cancer among MTHFR 677TT genotype with low folate intakes. A recent meta-analysis by Boccia et al. [
21], which included stratified analysis according to dietary folate intake, showed an increased risk for individuals with low folate intake (OR = 1.28, 95% CI = 0.97-1.68 for lung) versus high folate intake (OR = 0.94, 95% CI = 0.79-1.12 for lung). Plasma folate level might be relatively high among Korean adults; the median plasma folate was 22.7 nmol/L in our population based controls, which is higher than that in Chinese population [
22], and also higher than that in populations from15 European countries (folate status ranged from 6.3 to 20.1 nmol/L) [
23]. In addition, folate intake seems also fairly high among Korean population; the average of folate intake in Korea is about 347 μg/day [
24]. This level is higher than the average intake in most European countries, except for United Kingdom [
23]. This might provide a partial explanation why the MTHFR 677 mutations were found to protect against lung cancer, especially in lung squamous cell carcinoma in our study. Moreover, our recent study found a protective effect of MTHFR 677 T allele on the risk of gastric and colorectal cancer in a Korean population [
25].
In our study, there was no significant gender difference in the effect of MTHFR C677T polymorphism on lung cancer risk. Our results seem to differ from those of the Shi et al. [
26] study in Houston, TX, USA, which reported that the MTHFR 677TT genotype in women was associated with a decreased lung cancer risk compared with carriers of the MTHFR 677CC genotype.
Cigarette smoking is a known risk factor for lung cancer, and smokers may tend to have lower levels of serum and produce a localized deficiency of folic acid. We further examined the effects of MTHFR C677T in subgroups according to smoking status and found no interaction between the MTHFR C677T polymorphism and smoking. Our results seem somewhat similar to the results of Vineis, et al. [
18], which showed that the MTHFR C677T polymorphism had no any association in both smokers and nonsmokers. However, a beneficial effect of the MTHFR TT genotype on the risk of lung cancer was observed in those with heavy smokers; Suzuki et al. [
15] in Japan found that MTHFR 677T alleles were associated with reduced risk of squamous/small cell carcinomas, especially among heavy smokers with the MTHFR 677T allele. Liu et al. [
14] in Taiwan observed that smokers carrying the MTHFR 677 T allele showed a significantly decreased risk of lung cancer.
It is well known that familial aggregation of lung cancer could increase the risk of lung cancer, and a high consumption of vegetables and fruits is associated with a reduced risk of lung cancer. However, we have no information on the accuracy of reported family history of cancer, dietary folate intake or detailed data on the environmental tobacco exposure risk factors for lung cancer. Thus, we cannot evaluate the relationship between gene-environment interactions. Another limitation of the present study is that the case group was composed of lung cancer patients who were enrolled from hospital, which could not be representative the general population.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
MHS planned the analysis. CLH performed in the study design and drafted the manuscript. HNK and HRS participated in the experiments. JMP performed data analysis. YCK, IJO and KSK provided clinical material. SSK, JSC, and WJY participated in its design and coordination. All authors read and approved the final manuscript.