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Lack of Association Between CYP1A1 Polymorphisms and Risk of Bladder Cancer: a Meta-analysis

  • Lu, Yu (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Zhang, Xiao-Lian (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Xie, Li (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Li, Tai-Jie (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • He, Yu (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Peng, Qi-Liu (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Deng, Yan (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Wang, Jian (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Qin, Xue (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University) ;
  • Li, Shan (Department of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University)
  • Published : 2014.05.15

Abstract

Background: The effects of CYP1A1 gene polymorphisms on the risk of bladder cancer (BC) remain controversial. We carried out a meta-analysis to clarify the role of CYP1A1 gene polymorphisms in BC. Material and Methods: A comprehensive literature search was conducted up to November 20, 2013. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to estimate the strength of the association. Meta-regression, subgroup analysis, sensitivity analysis and publication bias were also performed. Results: Eight studies involving 1,059 BC cases and 1,061 controls were included. The meta-analysis showed that there was no significant association between the two common mutations of CYP1A1 and BC risk. For the I1e462Val A/G polymorphism with GG vs. AA the OR was 1.47 (95 % CI= 0.70-3.07, P =0.308). For the MspI T/C polymorphism, though a slight trend was found this was not statistically nonsignificant (CC vs.TT, OR = 1.24, 95 % CI= 0.98-1.58, P =0.078). Subgroup analyses by ethnicity also found no obvious association between CYP1A1 and BC risk. Conclusion: The present meta-analysis suggests that CYP1A1 polymorphism is not associated with bladder cancer risk.

Keywords

References

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