Association of DNA repair gene polymorphisms with genotoxic stress in underground coal miners

Mutagenesis. 2017 Oct 17;32(5):501-509. doi: 10.1093/mutage/gex018.

Abstract

In underground coal mining, numerous harmful substances and ionising radiation pose a major threat to the occupational safety and health of workers. Because cell DNA repair machinery eliminates genotoxic stress conferred by these agents, we examined whether single nucleotide polymorphisms in hOGG1 (rs1052133), XRCC1 (rs25487), ADPRT (rs1136410), XRCC4 (rs6869366) and LIG4 (rs1805388) genes modulate the genotoxic damage assessed by the cytokinesis-block micronucleus assay in lymphocytes from 143 underground coal miners and 127 healthy non-exposed males. We also analyzed models of gene-gene interactions associated with increased cytogenetic damage in coal miners and determined 'protective' and 'risk' combinations of alleles. We showed that miners with the G/G genotype of the hOGG1 (rs1052133) gene had a significantly increased frequency of binucleated lymphocytes with micronuclei (13.17‰, 95% CI = 10.78-15.56) compared to the C/C genotype carriers (10.35‰, 95% CI = 9.59-11.18). In addition, in the exposed group this indicator was significantly increased in carriers of the T/T genotype of the LIG4 (rs1805388) gene compared to miners harbouring the C/T genotype (13.00‰, 95% CI = 10.96-15.04 and 9.69‰, 95% CI = 8.32-11.06, respectively). Using the multifactor dimensionality reduction method, we found the three-locus model of gene-gene interactions hOGG1 (rs1052133) × ADPRT (rs1136410) × XRCC4 (rs6869366) associated with high genotoxic risk in coal miners. These results indicate that the studied polymorphisms and their combinations are associated with cytogenetic status in miners and may be used as molecular predictors of occupational risks in underground coal mines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Coal Mining
  • DNA / metabolism
  • DNA Damage
  • DNA Glycosylases / genetics
  • DNA Glycosylases / metabolism
  • DNA Ligase ATP / genetics
  • DNA Ligase ATP / metabolism
  • DNA Repair / genetics*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Humans
  • Lymphocytes / metabolism*
  • Male
  • Micronuclei, Chromosome-Defective / chemically induced*
  • Micronucleus Tests
  • Middle Aged
  • Miners*
  • Poly (ADP-Ribose) Polymerase-1 / genetics
  • Poly (ADP-Ribose) Polymerase-1 / metabolism
  • Polymorphism, Single Nucleotide*
  • Young Adult

Substances

  • DNA-Binding Proteins
  • LIG4 protein, human
  • XRCC4 protein, human
  • DNA
  • PARP1 protein, human
  • Poly (ADP-Ribose) Polymerase-1
  • DNA Glycosylases
  • oxoguanine glycosylase 1, human
  • DNA Ligase ATP