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Association Between MDM2 SNP309 T>G and Risk of Gastric Cancer: A Meta-analysis

  • Tian, Xin (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Tian, Ye (Department of Thoracic Surgery, the Fouth Affiliated Hospital of China Medical University) ;
  • Ma, Ping (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Sui, Cheng-Guang (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Meng, Fan-Dong (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Li, Yan (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Fu, Li-Ye (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Jiang, Tao (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Wang, Yang (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University) ;
  • Ji, Fu-Jian (Department of General Surgery, Second Hospital of Jilin University (Disease Treatment Center of Jilin University General Surgery)) ;
  • Fang, Xue-Dong (Department of General Surgery, Second Hospital of Jilin University (Disease Treatment Center of Jilin University General Surgery)) ;
  • Jiang, You-Hong (Molecular Oncology Department of Cancer Research Institute, the First Affiliated Hospital, China Medical University)
  • Published : 2013.03.30

Abstract

Background: As a negative regulator of P53, MDM2 plays an important role in carcinogenesis; a polymorphism in its promoter region. SNP309 T>G, is known to increase the expression of MDM2, thus being considered related to higher susceptibility to neoplasia. However, no agreement has been achieved regarding its effects on gastric cancer. Methods: The present systematic meta-analysis was performed based on comprehensive literature search from Pubmed, Web of science and CBM databases. Results: It was suggested from 6 independent studies that the GG genotype is associated with a significantly increased risk of gastric cancer (Recessive: OR = 1.43, 95% CI = 1.08-1.91, P = 0.013), and subgroup analysis also confirmed the relationship (English publications-recessive model: OR = 1.45, 95% CI = 1.10-1.91, P = 0.009; Studies in China-recessive model: OR = 1.58, 95% CI = 1.08-2.30, P = 0.017). No publication bias was detected. Conclusion: The meta-analysis indicated a significant inverse association between GG genotype carriage and elevated risk of gastric cancer. However, more studies and detailed information are needed to fully address the topic.

Keywords

References

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