Modifying Effect of Smoking on GSTM1 and NAT2 in Relation to the Risk of Bladder Cancer in Mongolian Population: A Case-Control Study
- PMID: 34452561
- PMCID: PMC8629459
- DOI: 10.31557/APJCP.2021.22.8.2479
Modifying Effect of Smoking on GSTM1 and NAT2 in Relation to the Risk of Bladder Cancer in Mongolian Population: A Case-Control Study
Abstract
Objectives: Tobacco smoking is the predominant risk factor for bladder cancer as it contains cancer-causing chemicals. However, genetic factors may play important role in response towards chemical carcinogens. In this study we aim to investigate genetic polymorphisms of glutathione S-transferase M1 (GSTM1) and N-acetyltransferase 2 (NAT2) as determinants of bladder cancer risk, independently and in combination with tobacco use in the Mongolian population.
Materials and methods: The current study was a hospital-based case-control study including 60 histologically confirmed bladder cancer patients and 60 cancer-free controls. PCR-RFLP assay was used to determine the presence of GSTM1 and NAT2 polymorphisms in bladder cancer patients and controls. GSTM1 and NAT2 were tested using binary logistical regression analysis with adjustment or stratification according to the smoking.
Results: There were 46 men and 14 women diagnosed with bladder cancer, with mean age was 58±4. The controls included 37 men and 23 women with a mean age of 57±3. The frequency of GSTM1 null genotype was higher in controls (71.67%) than in bladder cancer patients (58.33%) without statistical significance (OR=0.5534; 95% CI=0.2586-1.1843), (p=0.128). The NAT2 low acetylator phenotype was more common in patients with bladder cancer (15%) than in controls (5%). Furthermore, individuals with NAT2 low acetylator phenotype had a nearly 3.35-fold increased risk to develop bladder cancer (OR=3.35; 95% CI=0.8604-13.0657), (p=0.081) while the risk was even higher when combined with null GSTM1 genotype (OR=4; 95% CI=0.4459-37.5308), (p=0.213) but there was no statistical significance. Prevalence of smoking in bladder cancer patients was higher than controls and increased significantly the risk of bladder cancer (OR=8.31; 95% CI=3.66-18.88). Smokers with GSTM1 null genotype were at 5-fold higher risk of bladder cancer (OR=5.0; 95% CI=1.55-16.16), (p=0.007) while NAT2 low acetylator phenotype increased bladder cancer risk by 20-fold (OR=20.5; 95% CI=2.33-80.86), (p=0.006).
Conclusion: The current study shows that tobacco smokers with the NAT2 low acetylator phenotype and GSTM1 null genotype have the highest risk of bladder cancer in the Mongolian population.<br />.
Keywords: Glutathione S-transferase M1; Mongolia; N-acetyltransferase 2; bladder cancer; smoking.
Similar articles
-
NAT2 slow acetylation, GSTM1 null genotype, and risk of bladder cancer: results from the Spanish Bladder Cancer Study and meta-analyses.Lancet. 2005 Aug 20-26;366(9486):649-59. doi: 10.1016/S0140-6736(05)67137-1. Lancet. 2005. PMID: 16112301 Free PMC article.
-
Association of NAT2, GSTM1, GSTT1, CYP2A6, and CYP2A13 gene polymorphisms with susceptibility and clinicopathologic characteristics of bladder cancer in Central China.Cancer Detect Prev. 2009;32(5-6):416-23. doi: 10.1016/j.cdp.2009.02.003. Epub 2009 Mar 20. Cancer Detect Prev. 2009. PMID: 19303722
-
Arylamine N-acetyltransferase 1 (NAT1) and 2 (NAT2) polymorphisms in susceptibility to bladder cancer: the influence of smoking.Cancer Epidemiol Biomarkers Prev. 1997 Apr;6(4):225-31. Cancer Epidemiol Biomarkers Prev. 1997. PMID: 9107426
-
Polymorphisms in xenobiotic conjugation and disease predisposition.Toxicol Lett. 1998 Dec 28;102-103:173-83. doi: 10.1016/s0378-4274(98)00304-x. Toxicol Lett. 1998. PMID: 10022251 Review.
-
N-acetyltransferase 2 and bladder cancer: an overview and consideration of the evidence for gene-environment interaction.Br J Cancer. 2000 Aug;83(3):412-7. doi: 10.1054/bjoc.2000.1265. Br J Cancer. 2000. PMID: 10917561 Free PMC article. Review.
Cited by
-
Differences in β-naphthylamine metabolism and toxicity in Chinese hamster ovary cell lines transfected with human CYP1A2 and NAT2*4, NAT2*5B or NAT2*7B N-acetyltransferase 2 haplotypes.Arch Toxicol. 2022 Nov;96(11):2999-3012. doi: 10.1007/s00204-022-03367-2. Epub 2022 Aug 30. Arch Toxicol. 2022. PMID: 36040704 Free PMC article.
-
The association between PSCA gene polymorphism and hepatocellular carcinoma risk.World J Surg Oncol. 2025 Jun 10;23(1):229. doi: 10.1186/s12957-025-03878-z. World J Surg Oncol. 2025. PMID: 40495136 Free PMC article.
References
-
- Arand M, Muhlbauer R, Hengstler J, et al. A multiplex polymerase chain reaction protocol for the simultaneous analysis of the glutathione s-transferase GSTM1 and GSTT1 polymorphisms. Anal Biochem. 1996;236:184–6. - PubMed
-
- Bell DA, Taylor JA, Butler MA, et al. Genotype/phenotype discordance for human arylamine n-acetyltransferase (NAT2) reveals a new slow-acetylator allele common in African-Americans. Carcinogenesis. 1993;14:1689–92. - PubMed
-
- Bell DA, Taylor JA, Paulson DF, et al. Genetic risk and carcinogen exposure: a common inherited defect of the carcinogen-metabolism gene glutathione s-transferase M1 (GSTM1) that increases susceptibility to bladder cancer. J Natl Cancer Inst. 1993;85:1159–64. - PubMed
-
- Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68:394–424. - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous