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2017 | 30 | 5 | 791-802

Article title

Combined effects of NQO1 Pro187Ser or SULT1A1 Arg213His polymorphism and smoking on bladder cancer risk: Two meta-analyses

Content

Title variants

Languages of publication

Abstracts

EN
Objectives Objectives: Cigarette smoking is the major risk factor of bladder cancer via exposure to chemical carcinogens. Nicotinamide adenine dinucleotide phosphate (NADP+): quinine oxidoreductase 1 (NQO1) and sulfotransferase 1A1 (SULT1A1) have been reported to involve in the metabolism of polycyclic aromatic hydrocarbons (PAHs) and aromatic amines. Therefore, the risk of bladder cancer (BC) may be influenced by polymorphisms in the genes that modulate metabolic detoxification in particular by interacting with cigarette smoking. Considering the limited power by the individual studies with a relatively small sample size, especially when analyzing the combined effect of polymorphisms in NQO1 and SULT1A1 genes and smoking, these 2 meta-analyses have aimed to clarify the combined effects of them on BC risk by integrating related studies. Material and Methods Two meta-analyses included 1341 cases and 1346 controls concerning NQO1 Pro187Ser and smoking, and 1921 cases and 1882 controls on SULT1A1 Arg213His and smoking were performed. Odds ratios (OR) and 95% confidence intervals (CI) were used for assessing the strength of the association. Results The result has demonstrated that smokers with NQO1 Pro/Ser or Ser/Ser genotypes have a prominent association with the risk of BC as compared with non-smokers with NQO1 Pro/Pro genotype, with OR equal to 3.71 (95% CI: 2.87–4.78, $ \text{p}_\text{heterogeneity} $ = 0.376). Besides, smokers carrying SULT1A1 Arg/Arg genotypes were observed to confer 2.38 fold increased risk of BC (95% CI: 1.44–3.93, $ \text{p}_\text{heterogeneity} $ = 0.001) when compared with non-smokers with SULT1A1 Arg/Arg or His/His genotypes. Conclusions These findings have suggested that the NQO1 Pro187Ser or SULT1A1 Arg213His polymorphism combination with smoking significantly confer susceptibility to BC. Int J Occup Med Environ Health 2017;30(5):791–802

Year

Volume

30

Issue

5

Pages

791-802

Physical description

Dates

published
2017

Contributors

  • Medical College of Anhui University of Science and Technology, Huainan, China (Department of Pathogen Biology)
author
  • Medical College of Anhui University of Science and Technology, Huainan, China (Department of Pathogen Biology)
author
  • Medical College of Anhui University of Science and Technology, Huainan, China (Department of Biochemistry)
author
  • Medical College of Anhui University of Science and Technology, Huainan, China (Department of Biochemistry)
author
  • Medical College of Anhui University of Science and Technology, Huainan, China (Department of Pathogen Biology)

References

Document Type

Publication order reference

Identifiers

Biblioteka Nauki
2161894

YADDA identifier

bwmeta1.element.ojs-doi-10_13075_ijomeh_1896_00930
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