Possible associations of APE1 polymorphism with susceptibility and HOGG1 polymorphism with prognosis in gastric cancer

Anticancer Res. 2010 Apr;30(4):1359-64.

Abstract

Background: Multiple genetic and epigenetic alterations in several genes are implicated in the multistep process of human gastric carcinogenesis. In this study, we examined the polymorphisms of six DNA repair genes: APE1, HOGG1, XRCC1, XRCC3, XPD, and XPG in patients with gastric cancer (GC).

Patients and methods: Forty patients with GC and 247 controls were included in this study. DNA polymorphisms were determined by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) method.

Results: The frequency of the Asp/Glu genotype and Glu allele of APE1 in patients with GC was significantly higher than in the control group (p=0.05). We also observed a higher frequency of the Ser/Ser genotype of HOGG1 in grade III tumors, and in tumors with metastasis to adjacent tissue and solid organs (p<0.05).

Conclusion: Our results suggest that (i) APE1 gene polymorphism may be associated with GC risk and (ii) HOGG1 gene polymorphism may be informative in the prognosis of GC.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • DNA Glycosylases / genetics*
  • DNA Repair / genetics
  • DNA-(Apurinic or Apyrimidinic Site) Lyase / genetics*
  • DNA-Binding Proteins / genetics
  • Endonucleases / genetics
  • Genetic Predisposition to Disease
  • Humans
  • Middle Aged
  • Nuclear Proteins / genetics
  • Polymorphism, Genetic
  • Stomach Neoplasms / enzymology*
  • Stomach Neoplasms / genetics*
  • Transcription Factors / genetics
  • X-ray Repair Cross Complementing Protein 1
  • Xeroderma Pigmentosum Group D Protein / genetics

Substances

  • DNA excision repair protein ERCC-5
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Transcription Factors
  • X-ray Repair Cross Complementing Protein 1
  • X-ray repair cross complementing protein 3
  • XRCC1 protein, human
  • Endonucleases
  • DNA Glycosylases
  • oxoguanine glycosylase 1, human
  • Xeroderma Pigmentosum Group D Protein
  • APEX1 protein, human
  • DNA-(Apurinic or Apyrimidinic Site) Lyase
  • ERCC2 protein, human