[Analysis of the association of polymorphic variants of SYP1A2, GSTT1,GSTM1, GSTP1, XRCC1, XRCC3, AR and VDR genes with predisposition to the development of prostate cancer]

Vopr Onkol. 2016;62(5):632-637.
[Article in Russian]

Abstract

One of the risk factors for the development of malignant tumors, including prostate cancer, is an individual genetic predisposition due to the various unfavorable polymorphic variants of normal genes. The aim of the study was to com- pare the frequency of different genotypes of polymorphic vari- ants of genes CYPJA2, GSTT, GSTM, GSTP1 (xenobiotics detoxification), XRCC1, XRCC3,(DNA repair) and VDR, AR (transcription factors) in patients with prostate cancer and in control group to determine their association with genetic pre- disposition to this disease. According to the results obtained the rs1544410 AA genotype (VDR gene) and the presence of less than 20 CAG repeats in the 1st exon (AR gene) are the risk factors for the development of prostate cancer. The het- erozygous genotype 722 CT (XRCC3 gene) demonstrated the protective effect.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cytochrome P-450 CYP1A2 / genetics*
  • DNA-Binding Proteins / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Glutathione Transferase / genetics*
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Proteins / genetics*
  • Pregnancy
  • Prostatic Neoplasms / genetics*
  • Receptors, Androgen / genetics*
  • Receptors, Calcitriol / genetics*
  • X-ray Repair Cross Complementing Protein 1 / genetics*

Substances

  • AR protein, human
  • DNA-Binding Proteins
  • Neoplasm Proteins
  • Receptors, Androgen
  • Receptors, Calcitriol
  • VDR protein, human
  • X-ray Repair Cross Complementing Protein 1
  • X-ray repair cross complementing protein 3
  • XRCC1 protein, human
  • CYP1A2 protein, human
  • Cytochrome P-450 CYP1A2
  • glutathione S-transferase T1
  • Glutathione Transferase
  • glutathione S-transferase M1