• Title of article

    No Association between Estrogen Receptor #x392; Rs4986938 and Cancer Risk: A Systematic Review and MetaAnalysis

  • Author/Authors

    LI ، Zhaofang Institute of Endemic Diseases and Key Laboratory of Trace Elements and Endemic Diseases , YANG ، Xiaoli Institute of Endemic Diseases and Key Laboratory of Trace Elements and Endemic Diseases , ZHANG ، Rongqiang Institute of Endemic Diseases and Key Laboratory of Trace Elements and Endemic Diseases , LI ، Baorong Institute of Endemic Diseases and Key Laboratory of Trace Elements and Endemic Diseases , ZHANG ، Di Institute of Endemic Diseases and Key Laboratory of Trace Elements and Endemic Diseases , LI ، Qiang Institute of Endemic Diseases and Key Laboratory of Trace Elements and Endemic Diseases , XIONG ، Yongmin Institute of Endemic Diseases and Key Laboratory of Trace Elements and Endemic Diseases

  • Pages
    12
  • From page
    784
  • To page
    795
  • Abstract
    Background: The association between estrogen receptor #x3B2; (ESR2) rs4986938 polymorphism and the risk of various types of cancer have been investigated in previous studies. However, the results remained disputable. Here, we conducted a metaanalysis to investigate the association between ESR2 rs4986938 polymorphism and the risk of cancer. #xD; Methods: We searched for relevant articles collected by the PubMed, EMBASE, and Cochrane library up to March 30, 2018. The association was assessed using Odds ratios (ORs) and 95% confidence intervals (CIs). #xD; Results: The metaanalysis involved a total of 23 studies in 20 papers, including 24,334 cases and 31,707 controls. No significant association was detected between the rs4986938 polymorphism and cancer risk in the additive model (A compared with G: OR=0.97, 95% CI=0.921.02, P=0.20), dominant model (AA+AG compared with GG: OR=0.96, 95% CI=0.931.03, P=1.00), recessive model (AA compared with AG + GG: OR=0.94, 95% CI=0.861.03, P=0.18), heterozygous model (AG compared with GG: OR=0.97, 95% CI=0.941.01, P=0.14), and homozygous model (AA compared with GG: OR=0.96, 95% CI=0.871.06, P=0.39). Results of subgroup analysis stratified by ethnicity and cancer types further validated the results. #xD; Conclusion: We found no evidence of an association between rs4986938 and the risk of overall cancer. #xD; #xA0; #xD; #xA0;
  • Keywords
    ESR2 , Single nucleotide polymorphism , Cancer risk
  • Journal title
    Iranian Journal of Public Health
  • Serial Year
    2019
  • Journal title
    Iranian Journal of Public Health
  • Record number

    2464224