Role of Caspase-9 Gene Ex5+32 G>A (rs1052576) Variant in Susceptibility to Primary Brain Tumors

Anticancer Res. 2017 Sep;37(9):4997-5000. doi: 10.21873/anticanres.11912.

Abstract

Background/aim: This study is the first to evaluate the relationship of caspase-9 (CASP-9) gene polymorphism with the risk for primary brain tumor development.

Materials and methods: The study group included 43 glioma and 27 meningioma patients and 76 healthy individuals. CASP-9 gene Ex5+32 G>A (rs1052576) polymorphism was analyzed by real-time polymerase chain reaction (RT-PCR).

Results: Individuals with the CASP-9 GG genotype had significantly decreased risk of developing a glioma brain tumor (p=0.024). Additionally, the GA genotype was significantly lower in patients with glioma than the control group (p=0.019). A significantly decreased risk of developing glioma was found in the A allele carrier group (p=0.024). However, there was no statistically significant relationship between CASP-9 polymorphism and brain meningioma (p=0.493).

Conclusion: CASP-9 (rs1052576) mutant A allele seems to be a protective factor for glioma brain tumor. Future studies with a larger sample size will clarify the possible roles of CASP-9 gene in the etiology and progression of primary brain tumors.

Keywords: Caspase-9; glioma; meningioma; polymorphism.

MeSH terms

  • Biomarkers, Tumor / genetics*
  • Brain Neoplasms / genetics*
  • Case-Control Studies
  • Caspase 9 / genetics*
  • Female
  • Follow-Up Studies
  • Genetic Predisposition to Disease
  • Glioma / genetics*
  • Humans
  • Male
  • Meningeal Neoplasms / genetics*
  • Meningioma / genetics*
  • Middle Aged
  • Mutation
  • Neoplasm Staging
  • Polymorphism, Single Nucleotide / genetics*
  • Prognosis
  • Prospective Studies
  • Risk Factors

Substances

  • Biomarkers, Tumor
  • CASP9 protein, human
  • Caspase 9