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NQO1 C609T polymorphism and esophageal cancer risk: a HuGE review and meta-analysis

BMC Medical Genetics volume 14, Article number: 31 (2013) Cite this article

Abstract

Background

Many studies have been carried out to test the hypothesis that the NQO1 C609T polymorphism might be associated with the risk of esophageal cancer. However, the results are poorly consistent, partly due to genetic or other sources of heterogeneity. To investigate the association between this polymorphism and the risk of esophageal cancer, a meta-analysis was performed.

Methods

We used odds ratios (ORs) with 95% confidence intervals (CIs) to assess the strength of association. The frequency of the putative risk allele in the controls was estimated by the inverse-variance method. Cochran’s Q statistic and the inconsistency index (I2) were used to check heterogeneity. Egger’s test and an inverted funnel plot were used to assess the publication bias.

Results

Our study included eight published case-control studies about the NQO1 C609T polymorphism and esophageal cancer, including a total of 1,217 esophageal cancer patients and 1,560 controls. Overall, a significant association was found between the NQO1 C609T variant and esophageal cancer under a recessive model (OR = 1.647; 95% CI = 1.233-2.200). Regarding histological type, more significant evidence was found for esophageal squamous cell carcinoma (ESCC) (OR = 2.03; 95% CI = 1.29-3.19) than esophageal adenocarcinoma (EAC) (OR = 1.61; 95% CI = 1.01-2.56) under a recessive model.

Conclusions

The meta-analysis suggests that the NQO1 C609T polymorphism considerably increases the risk of esophageal cancer.

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Background

Esophageal cancer is a malignancy of the esophagus, the muscular tube through which food passes from the throat to the stomach. Esophageal tumors usually lead to dysphagia, pain and other symptoms, and are diagnosed by biopsy. Generally, esophageal cancer has two subtypes, squamous cell cancer (ESCC) and adenocarcinoma (EAC). Squamous cell cancer arises from the cells that line the upper part of the esophagus. Adenocarcinoma arises from glandular cells that are present at the junction of the esophagus and the stomach [1].

NAD(P)H quinone oxidoreductase 1 (NQO1) is a member of the NAD(P)H dehydrogenase (quinone) family and encodes a cytoplasmic 2-electron reductase, which is a cytosolic flavoenzyme that protects cells from oxidative damage [2]. NQO1 catalyzes the reductive activation of quinoid chemotherapeutic agents and environmental carcinogens such as heterocyclic amines, nitrosamines and cigarette smoke condensates [3]. The NQO1 T allele has only 2 to 4% enzymatic activity in comparison to its wild type form. Cells homozygous for the polymorphic NQO1 allele (T/T) express NQO1 mRNA, but not the protein because the mutant NQO1 protein is rapidly degraded by the proteasomal system [4]. However, the activity of the NQO1 enzyme may be influenced by a major polymorphism involving a single C to T substitution at nucleotide 609 of exon 6 in the NQO1 cDNA that causes a Pro187Ser amino acid change [5].

Some studies have shown that this polymorphism in the NQO1 gene affects the translation of the NQO1 protein. Compared to the homozygous wild type (C/C), expression of the NQO1 protein encoded by the heterozygous phenotype (C/T) is decreased approximately three-fold. In addition, the homozygous mutant (T/T) phenotype causes a complete lack of enzyme activity [3, 5–7]. The NQO1 C609T polymorphism has been associated with the risk of various cancers such as renal [8], lung [9, 10], esophageal [11–13], colorectal [14], and head and neck [15]. However, the results of some studies on the effect of the NQO1 C609T polymorphism on esophageal cancer are debatable. Meta-analyses are usually useful when many studies point more or less in the same direction, but a single study does not have sufficient power to show a significant result. Therefore, a meta-analysis of these studies was undertaken to investigate the association of the NQO1 C609T polymorphism with susceptibility to esophageal cancer.

Methods

Search strategy and data extraction

All original studies published in English on the NQO1 C609T polymorphism and esophageal cancer were considered in our meta-analysis. HuGENet, Embase and PubMed were searched up to August 8 2011, using the following terms: (“esophageal cancer” or “esophagus” or “ESCC” or “EAC” or “oesophagus”) and (“polymorphism” or “SNP” or “allele” or “variant”) and (“NQO1” or “NAD(P)H: quinine oxidoreductase 1” or “NAD(P)H dehydrogenase, quinone 1” or “DHQU”).

Included studies had to fit the following criteria: (1) sufficient data regarding allele frequency; (2) an association analysis between the NQO1 C609T polymorphism and esophageal cancer risk; and (3) independent case-control studies.

Data extraction

The following information was extracted by three investigators (Y-L H, W-W H and Y-H Z) from each study: the first author, year of publication, country, race, sample size, outcome, characteristics of controls, case and control diagnostic criteria, genotyping method, allele frequencies, genotype distribution in cases and controls, pathology status of esophageal cancer and the esophageal cancer risk factors. Results were compared and different opinions were resolved by a discussion.

Statistical analysis

Hardy-Weinberg equilibrium (HWE; P ≥ 1e-03) and chi-square test methods were used to test the distribution of genotypes in the control group of each study. The frequency of the putative risk allele in the controls was estimated by the inverse-variance method [16–18]. Cochran’s Q statistic and the inconsistency index (I2) were used to check heterogeneity [19]; if P > 0.10 and I2 < 25%, heterogeneity did not exist among the studies [20]. If there was no heterogeneity, logistic regression with fixed effects was used to evaluate the overall gene effect; otherwise, the random-effects model was used. To determine the overall gene effect, the model that included the gene was compared with the model that did not. If the overall gene effect was statistically significant, further comparisons of OR1 (AA vs. aa), OR2 (Aa vs. aa) and OR3 (AA vs. Aa) were explored with A as the risk allele. We selected the genetic models according to the following criteria [20]:

If OR1 = OR2 ≠ 1 and OR3 = 1, the dominant model was selected.

If OR1 = OR3 ≠ 1 and OR2 = 1, the recessive model was accepted.

If OR2 = 1/OR3 ≠ 1 and OR1 = 1, the overdominant model was taken.

If OR1 > OR2 > 1 and OR1 > OR3 > 1(or OR1 < OR2 < 1 and OR1 < OR3 < 1), the codominant model was adopted. Finally, the results were pooled again under the appropriate genetic model.

Egger’s test and an inverted funnel plot was used to assess publication bias [21]. HWE was checked in the control group of the eligible studies by the chi-square test (p ≤ 0.001). Sensitivity analysis was performed including studies that deviated from HWE. Statistical tests were performed using the STATA software, version 11.1 (Stata Corporation, USA). All P values were two-sided.

Results

Study inclusion and characteristics

Ten relevant studies describing the association between NQO1 C609T and esophageal cancer were identified. However, after reading the full text, we excluded two of these ten studies due to overlapping [22, 23]. Finally, eight studies met the inclusion criteria and were included [24–31]. Among these, five were on Caucasians [24, 26–29] and three on Asians [25, 30, 31]. All the included studies were case-controlled, comprising 1,217 cases and 1,560 controls.

Among the included articles described in Table 1, four selected esophageal cancer patients based on endoscopy or histological diagnosis [24–26, 31], while the other four [27–30] selected cases that underwent esophagectomy without prior radio- and/or chemotherapy. All the controls were recruited in the same period as the cases. However, the source of the controls for each study was not similar. In the included studies, five studies [27–31] selected healthy individuals as controls, while three [24–26] chose hospital patients as controls.

Table 1 The studies summary of NQO1 C609T polymorphism with esophageal cancer
Full size table

In addition, among these eligible studies, two included populations that were selected from ESCC patients [26, 29], four from EAC patients [24, 27, 28, 30], while the other two did not clarify the histological type [25, 31].

Meta-analysis database

Overall, the eligible studies included 1,124 cases and 1,510 controls that were genotyped. The prevalence rates of TT in C609T variants were 19.1% in the controls of Asian descent and 4.1% in the controls of Caucasian descent. The prevalence rates of CT for controls of Caucasian and Asian decent were 45.5% and 31.7%, respectively. For histological type, the prevalence rates of TT were 8.6% and 7.3% in controls of ESCC and EAC patients, respectively, while CT were 40.9% and 34.0% in controls of ESCC and EAC patients, respectively. The genotype distribution and all the P-values for HWE testing are shown in Tables 2 and 3.

Table 2 Frequency of NQO1 C609T polymorphism in different populations included in a meta-analysis
Full size table
Table 3 Frequency of NQO1 C609T polymorphism in ESCC and EAC patients included in a meta-analysis
Full size table

Main results, subgroup analyses

NQO1 C609T polymorphism and ethnic group

The results of the included studies regarding the association between the NQO1 C609T polymorphism and esophageal cancer were conflicting, as seen in Table 1. Hamajima et al [25], Rahden et al [28], Zhang et al [31] and Marjani et al [26] showed no significant association with esophageal cancer. However, the other four studies showed a significant association with esophageal cancer [24, 27, 29, 30]. All the included studies were in HWE.

After sensitivity analysis, Hamajima et al [25] and Martino et al [24] had the highest sensitivity, and were removed because the controls included no healthy people, which was determined by reading the full text. After removing these two articles, the phenotyped samples contained 974 cases and 1,226 controls.

Using the inverse variance fixed effects model, the ORs of the pooled NQO1 T allele frequencies were 1.32 (95% CI: 1.08-1.62) for Caucasians and 1.32 (95% CI: 1.08-1.60) for Asians. In total, the summary OR for all the studies was 1.32 (95% CI: 1.15-1.52). It was shown that the T allele was related to susceptibility to esophageal cancer.

According to the principle of genetic model selection by Thakkinstian [17], the recessive model was determined. The summary result showed a significant relationship between the NQO1 C609T polymorphism and esophageal cancer (Figure 1) from the meta-analysis of the phenotype studies. For the recessive model, the overall pooled odds ratio using a fixed effect model was 1.65 (95% CI: 1.23-2.20). The ORs for Caucasians and Asians were 2.03 (95% CI:1.14-3.61) and 1.53 (95% CI:1.10-2.14), respectively. Through heterogeneity analysis, we found no evidence for heterogeneity among the studies (for the recessive model, I2 = 0.0%, P = 0.48). In addition, Egger’s test showed that publication bias was not significant under the recessive model (P = 0.69).

Figure 1
figure 1

The forest plot describing the meta- analysis with a fixed-effect recessive model (TT versus CT + CC) for the association of NQO1 C609T polymorphism with esophageal cancer. Each study is depicted with size inversely proportional to its variance, accompanied by the respective 95% confidence intervals. Values of OR > 1, implied an increased risk for esophageal cancer with the TT genotype.

Full size image

NQO1 C609T polymorphism and histological type of esophageal cancer

Six case-control articles reporting an association between the NQO1 C609T polymorphism and the histological type of esophageal cancer were included in our research, but their results were debatable. For EAC, Martino et al [24] and Zhang et al [30] showed a significant association, but Rahden et al [28] showed no significant correlation. For ESCC, Sarbia et al [27] and Zhang et al [29] showed a significant association, but Marjani et al [26] did not. After removing this study, the samples of different histological types contained 868 cases and 1,120 controls.

The recessive model was selected according to the principle of Thakkinstian [17]. The summary result from the meta-analysis of the phenotype studies indicated a significant relationship between the NQO1 C609T polymorphism and the histological type of esophageal cancer (Figure 2). For the recessive model, the overall pooled odds ratio using the fixed effect model was 1.82 (95% CI: 1.32-2.52). The ORs of ESCC and EAC were 2.03 (95% CI:1.29-3.19) and 1.61 (95% CI:1.01-2.56), respectively. Through heterogeneity analysis, we found no evidence for heterogeneity among the studies (for the recessive model, I2 = 0.0%, P = 0.44). Finally, Egger’s test showed that publication bias was not significant under the recessive model (P = 0.74).

Figure 2
figure 2

The forest plot describing the meta- analysis with a fixed-effect recessive model (TT versus CT + CC) for the association of NQO1 C609T polymorphism with ESCC and EAC. Each study is depicted with size inversely proportional to its variance, accompanied by the respective 95% confidence intervals. Values of OR > 1, implied an increased risk for esophageal cancer with the TT genotype.

Full size image

To test whether heterogeneity of the samples affected the results of the meta-analysis, we performed additional analysis. We only used the samples from Germany and China to test the ethnicity effect. The ORs of Germany and China were 1.68 (95% CI: 1.13-2.51) and 1.96 (95% CI: 1.36-2.82), respectively. There was no obvious difference in the results from Caucasian and Asian patients.

Discussion

NQO1 acts as an imperative part of the cellular antioxidant defense system by detoxifying quinines and can prevent the formation of reactive oxygen species. NQO1 gene mutations are linked to tardive dyskinesia, which increases the risk of hematotoxicity after exposure to benzene, and susceptibility to various forms of cancer. Many studies have been carried out to test the hypothesis that the NQO1 C609T polymorphism might be linked to the risk of esophageal cancer, but the results are controversial. This meta-analysis, involving a total of 1,217 esophageal cancer patients and 1,560 controls from eight case-control studies, examined the association of one polymorphisms of the NQO1 gene with esophageal cancer risk. The OR of the pooled NQO1 T allele frequencies for all the studies was 1.32 (95% CI: 1.15-1.52). In addition, significant evidence was found for a correlation between the NQO1 C609T variant and esophageal cancer under the recessive model (OR = 1.647; 95%CI = 1.233-2.200). Similar to our study, other reports have also shown an association of NQO1 609C > T polymorphism with susceptibility to esophageal tumors. Marjani et al [26] observed that NQO1 expression in esophageal tumor tissue was related to the NOQ1C609T genotype, with its expression elevated when the T allele appeared in the NOQ1C609T genotype.

Different enzymes encoded by varying NQO1genotypes may affect enzyme activities, and the lack of NQO1 activity encoded by the homozygous TT genotype might result in reduced detoxification of exogenous carcinogens. Traver et al [32] confirmed that the NQO1 homozygous variant (TT) had very little or no quinine reductase activity; however, compared to the homozygote (CC), the heterozygote variant (CT) showed approximately one-third of the enzymatic activity. Recent studies have identified a C➙ T mutation in NQO1 [33]. Two to 4% of the global human population carry both mutant alleles and are deficient in NQO1. Mice lacking NQO1 gene expression accumulate lower amounts of abdominal fat and show increased sensitivity to menadione-induced hepatic toxicity compared to wild type mice [11, 12]. Delwin et al [13] showed that loss of NQO1 caused mycloid hyperplasia of the bone marrow and significant increases in blood neutrophils, eosinophils and basophils in NQO1-null mice.

A heterogeneity evaluation is always conducted in statistical analysis in meta-analysis. However, we found low statistical power during heterogeneity testing. Therefore, several subgroup meta-analyses were performed according to ethnicity, control source and case classification. In the racial subgroups, there was a statistically significant asssociation between the NQO1 polymorphism and esophageal cancer. The ORs for Caucasians and Asians were 2.03 (95% CI:1.14-3.61) and 1.53 (95% CI:1.10-2.14), respectively. This showed a possible role of ethnic divergence. Wang et al [34] also noted that the overall frequency of the NQO1 609 T allele was nearly double among Asians than in Europeans in both patients and controls. There is a wide ethnic variation in allelic frequencies of NQO1 609C > T according to the Hapmap database (http://www.hapmap.ncbi.nlm.nih.gov): 18.6% in Europeans (CEU) and 50% in Asian populations (HCB).

The results of this meta-analysis should be interpreted with some caution because there were limitations in our analysis. First, selection bias was a possible major source of heterogeneity from uncontrolled confounders and bias inherent in the study design. For example, there was not an identical criterion for cases and controls among all the included articles. Second, different genotype ratios may have a potential impact on the outcomes. The rate of the TT genotype was very low in Caucasian subjects (fewer than 10% of all Caucasian studies), but showed a moderate distribution in Asians (more than 15% in all Asian studies). Third, we only considered the NQO1 C609T polymorphism in esophageal cancer. However, there may be a possible interaction between the NQO1 C609T polymorphism and other environmental factors.

Conclusions

In summary, the present meta-analysis provides information that the NQO1 C609T polymorphism considerably increases susceptibility to or prognosis of esophageal cancer, especially in ESCC patients. Additional population-based studies in large sample sizes should be conducted before its clinical application.

References

  1. Enzinger PC, Mayer RJ: Esophageal cancer. N Engl J Med. 2003, 349 (23): 2241-2252. 10.1056/NEJMra035010.

    Article  CAS  PubMed  Google Scholar 

  2. Nebert DW, Roe AL, Vandale SE, Bingham E, Oakley GG: NAD(P)H:quinone oxidoreductase (NQO1) polymorphism, exposure to benzene, and predisposition to disease: a HuGE review. Genet Med. 2002, 4 (2): 62-70. 10.1097/00125817-200203000-00003.

    Article  CAS  PubMed  Google Scholar 

  3. Larson RA, Wang Y, Banerjee M, Wiemels J, Hartford C, Le Beau MM, Smith MT: Prevalence of the inactivating 609C→T polymorphism in the NAD(P)H:quinone oxidoreductase (NQO1) gene in patients with primary and therapy-related myeloid leukemia. Blood. 1999, 94 (2): 803-807.

    CAS  PubMed  Google Scholar 

  4. Siegel D, Anwar A, Winski SL, Kepa JK, Zolman KL, Ross D: Rapid polyubiquitination and proteasomal degradation of a mutant form of NAD(P)H: quinone oxidoreductase 1. Mol Pharmacol. 2001, 59 (2): 263-268.

    CAS  PubMed  Google Scholar 

  5. Kuehl BL, Paterson JW, Peacock JW, Paterson MC, Rauth AM: Presence of a heterozygous substitution and its relationship to DT-diaphorase activity. Br J Cancer. 1995, 72 (3): 555-561. 10.1038/bjc.1995.373.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Moran JL, Siegel D, Ross D: A potential mechanism underlying the increased susceptibility of individuals with a polymorphism in NAD(P)H:quinone oxidoreductase 1 (NQO1) to benzene toxicity. Proc Natl Acad Sci USA. 1999, 96 (14): 8150-8155. 10.1073/pnas.96.14.8150.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Smith MT: Benzene, NQO1, and genetic susceptibility to cancer. Proc Natl Acad Sci USA. 1999, 96 (14): 7624-7626. 10.1073/pnas.96.14.7624.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Schulz WA, Krummeck A, Rosinger I, Eickelmann P, Neuhaus C, Ebert T, Schmitz-Drager BJ, Sies H: Increased frequency of a null-allele for NAD(P)H: quinone oxidoreductase in patients with urological malignancies. Pharmacogenetics. 1997, 7 (3): 235-239. 10.1097/00008571-199706000-00008.

    Article  CAS  PubMed  Google Scholar 

  9. Chen H, Lum A, Seifried A, Wilkens LR, Le Marchand L: Association of the NAD(P)H:quinone oxidoreductase 609C→T polymorphism with a decreased lung cancer risk. Cancer Res. 1999, 59 (13): 3045-3048.

    CAS  PubMed  Google Scholar 

  10. Xu LL, Wain JC, Miller DP, Thurston SW, Su L, Lynch TJ, Christiani DC: The NAD(P)H:quinone oxidoreductase 1 gene polymorphism and lung cancer: differential susceptibility based on smoking behavior. Cancer Epidemiol Biomarkers Prev. 2001, 10 (4): 303-309.

    CAS  PubMed  Google Scholar 

  11. Radjendirane V, Joseph P, Lee YH, Kimura S, Klein-Szanto AJ, Gonzalez FJ, Jaiswal AK: Disruption of the DT diaphorase (NQO1) gene in mice leads to increased menadione toxicity. J Biol Chem. 1998, 273 (13): 7382-7389. 10.1074/jbc.273.13.7382.

    Article  CAS  PubMed  Google Scholar 

  12. Klaidman LK, Leung AC, Adams JD: High-performance liquid chromatography analysis of oxidized and reduced pyridine dinucleotides in specific brain regions. Anal Biochem. 1995, 228 (2): 312-317. 10.1006/abio.1995.1356.

    Article  CAS  PubMed  Google Scholar 

  13. Long DJ, Gaikwad A, Multani A, Pathak S, Montgomery CA, Gonzalez FJ, Jaiswal AK: Disruption of the NAD(P)H:quinone oxidoreductase 1 (NQO1) gene in mice causes myelogenous hyperplasia. Cancer Res. 2002, 62 (11): 3030-3036.

    CAS  PubMed  Google Scholar 

  14. Sameer AS, Shah ZA, Syeed N, Rasool R, Afroze D, Siddiqi MA: NAD(P)H:quinone oxidoreductase 1 (NQO1) Pro187Ser polymorphism and colorectal cancer predisposition in the ethnic Kashmiri population. Asian Pac j cancer prev: APJCP. 2010, 11 (1): 209-213.

    PubMed  Google Scholar 

  15. Cho CG, Lee SK, Nam SY, Lee MS, Lee SW, Choi EK, Park HJ, Kim SY: Association of the GSTP1 and NQO1 polymorphisms and head and neck squamous cell carcinoma risk. J Korean Med Sci. 2006, 21 (6): 1075-1079. 10.3346/jkms.2006.21.6.1075.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Ioannidis JP, Ntzani EE, Trikalinos TA: ‘Racial’ differences in genetic effects for complex diseases. Nat Genet. 2004, 36 (12): 1312-1318. 10.1038/ng1474.

    Article  CAS  PubMed  Google Scholar 

  17. Thakkinstian A, McElduff P, D’Este C, Duffy D, Attia J: A method for meta-analysis of molecular association studies. Stat Med. 2005, 24 (9): 1291-1306. 10.1002/sim.2010.

    Article  PubMed  Google Scholar 

  18. Thakkinstian A, McEvoy M, Minelli C, Gibson P, Hancox B, Duffy D, Thompson J, Hall I, Kaufman J, Leung TF: Systematic review and meta-analysis of the association between {beta}2-adrenoceptor polymorphisms and asthma: a HuGE review. Am J Epidemiol. 2005, 162 (3): 201-211. 10.1093/aje/kwi184.

    Article  PubMed  Google Scholar 

  19. Petiti DB: Meta-analysis, decision analysis, and cost-effectiveness analysis. 1994, Oxford: Oxford University Press

    Google Scholar 

  20. Higgins JP, Thompson SG, Deeks JJ, Altman DG: Measuring inconsistency in meta-analyses. BMJ. 2003, 327 (7414): 557-560. 10.1136/bmj.327.7414.557.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Egger M, Davey Smith G, Schneider M, Minder C: Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997, 315 (7109): 629-634. 10.1136/bmj.315.7109.629.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Li Y, Zhang JH, Guo W, Wang R, Wen DG, Wei LZ: Polymorphism of NAD(P)H dehydrogenase (quinone) 1 (NQO1) C 609 T and risk of esophageal neoplasm. Zhonghua Liu Xing Bing Xue Za Zhi. 2004, 25 (8): 731-

    CAS  PubMed  Google Scholar 

  23. Zhang JH, Li Y, Wang R, Sarbia M, Guo W, Wen DG, Wei LZ, Chen ZF, Kuang G, Zhang LW: The NAD(P)H: quinone oxidoreductase 1 C609T polymorphism and susceptibility to esophageal cancer. Zhonghua Xue Yi Chuan Xue Za Zhi. 2003, 20 (6): 544-546.

    CAS  Google Scholar 

  24. di Martino E, Hardie LJ, Wild CP, Gong YY, Olliver JR, Gough MD, Bird NC: The NAD(P)H:quinone oxidoreductase I C609T polymorphism modifies the risk of Barrett esophagus and esophageal adenocarcinoma. Genet Med. 2007, 9 (6): 341-347. 10.1097/GIM.0b013e3180654ccd.

    Article  CAS  PubMed  Google Scholar 

  25. Hamajima N, Matsuo K, Iwata H, Shinoda M, Yamamura Y, Kato T, Hatooka S, Mitsudomi T, Suyama M, Kagami Y: NAD(P)H: quinone oxidoreductase 1 (NQO1) C609T polymorphism and the risk of eight cancers for Japanese. Int J Clin Oncol. 2002, 7 (2): 103-108.

    CAS  PubMed  Google Scholar 

  26. Marjani HA, Biramijamal F, Rakhshani N, Hossein-Nezhad A, Malekzadeh R: Investigation of NQO1 genetic polymorphism, NQO1 gene expression and PAH-DNA adducts in ESCC. A case-control study from Iran Genet Mol Res. 2010, 9 (1): 239-249.

    CAS  PubMed  Google Scholar 

  27. Sarbia M, Bitzer M, Siegel D, Ross D, Schulz WA, Zotz RB, Kiel S, Geddert H, Kandemir Y, Walter A: Association between NAD(P)H: quinone oxidoreductase 1 (NQ01) inactivating C609T polymorphism and adenocarcinoma of the upper gastrointestinal tract. Int J Cancer. 2003, 107 (3): 381-386. 10.1002/ijc.11430.

    Article  CAS  PubMed  Google Scholar 

  28. von Rahden BH, Stein HJ, Langer R, von Weyhern CW, Schenk E, Doring C, Siewert JR, Hofler H, Sarbia M: C609T polymorphism of the NAD(P)H:quinone oxidoreductase I gene does not significantly affect susceptibility for esophageal adenocarcinoma. Int J Cancer. 2005, 113 (3): 506-508. 10.1002/ijc.20576.

    Article  CAS  PubMed  Google Scholar 

  29. Zhang J, Schulz WA, Li Y, Wang R, Zotz R, Wen D, Siegel D, Ross D, Gabbert HE, Sarbia M: Association of NAD(P)H: quinone oxidoreductase 1 (NQO1) C609T polymorphism with esophageal squamous cell carcinoma in a German Caucasian and a northern Chinese population. Carcinogenesis. 2003, 24 (5): 905-909. 10.1093/carcin/bgg019.

    Article  PubMed  Google Scholar 

  30. Zhang JH, Li Y, Wang R, Geddert H, Guo W, Wen DG, Chen ZF, Wei LZ, Kuang G, He M: NQO1 C609T polymorphism associated with esophageal cancer and gastric cardiac carcinoma in North China. World J Gastroenterol. 2003, 9 (7): 1390-1393.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Zhang WC, Yin LH, Pu YP, Liang GY, Hu X, Liu YZ, Cui YS: Relationship between quinone oxidoreductase1 gene ns-cSNP and genetic susceptibility of esophageal cancer. Zhonghua Yu Fang Yi Xue Za Zhi. 2006, 40 (5): 324-327.

    CAS  PubMed  Google Scholar 

  32. Traver RD, Horikoshi T, Danenberg KD, Stadlbauer TH, Danenberg PV, Ross D, Gibson NW: NAD(P)H:quinone oxidoreductase gene expression in human colon carcinoma cells: characterization of a mutation which modulates DT-diaphorase activity and mitomycin sensitivity. Cancer Res. 1992, 52 (4): 797-802.

    CAS  PubMed  Google Scholar 

  33. Rauth AM, Goldberg Z, Misra V: DT-diaphorase: possible roles in cancer chemotherapy and carcinogenesis. Oncol Res. 1997, 9 (6–7): 339-349.

    CAS  PubMed  Google Scholar 

  34. Wang Z, Hu J, Zhong J: Meta-analysis of the NAD(P)H: quinine oxidoreductase 1 gene 609 C > T polymorphism with esophageal cancer risk. DNA Cell Biol. 2012, 31 (4): 560-567. 10.1089/dna.2011.1332.

    Article  PubMed  Google Scholar 

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Acknowledgments

This work was supported by the National Natural Science Foundation of China (grant no. 81060213), Guangxi Natural Science Foundation (grant no. 2011GXNSFB018100, 2010GXNSFB013061).

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    Authors and Affiliations

    1. Medical Research Center of Guangxi Medical University, Nanning, Guangxi, China

      Hu Yanling

    2. Department of gastro enterology, First Affiliated Hospital, Guangxi Medical University, Nanning, Guangxi, China

      Zhang Yuhong

    3. Department of Cardiothoracic Surgery, First Affiliated Hospital, Guangxi Medical University, Nanning, Guangxi, China

      He Wenwu, Xian Lei & Chen Mingwu

    4. Department of Cardiothoracic Surgery, Nanchong Central Hospital • The Second Clinical College of North Sichuan Medical college, Nanchong, Sichuan, China

      He Wenwu

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    Correspondence to Chen Mingwu.

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    Authors’ contributions

    YH collected the literature data, developed the statistical model, carried out the software implementation and drafted the manuscript. WH collected the literature data, read the full text articles, and checked the model and results. YZ collected the literature data, read the full text articles and drafted the manuscript. XL helped with the discussion in theoretical developments, as well as in drafting the manuscript. MC helped with the discussion both in the theoretical development and English copyediting. All authors read and approved the final manuscript.

    Hu Yanling, Zhang Yuhong, He Wenwu contributed equally to this work.

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    Yanling, H., Yuhong, Z., Wenwu, H. et al. NQO1 C609T polymorphism and esophageal cancer risk: a HuGE review and meta-analysis. BMC Med Genet 14, 31 (2013). https://doi.org/10.1186/1471-2350-14-31

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    • DOI: https://doi.org/10.1186/1471-2350-14-31

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    BMC Medical Genetics

    ISSN: 1471-2350

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