Both genetic and dietary factors underlie individual differences in DNA damage levels and DNA repair capacity

DNA Repair (Amst). 2014 Apr:16:66-73. doi: 10.1016/j.dnarep.2014.01.016. Epub 2014 Mar 6.

Abstract

The interplay between dietary habits and individual genetic make-up is assumed to influence risk of cancer, via modulation of DNA integrity. Our aim was to characterize internal and external factors that underlie inter-individual variability in DNA damage and repair and to identify dietary habits beneficial for maintaining DNA integrity. Habitual diet was estimated in 340 healthy individuals using a food frequency questionnaire and biomarkers of antioxidant status were quantified in fasting blood samples. Markers of DNA integrity were represented by DNA strand breaks, oxidized purines, oxidized pyrimidines and a sum of all three as total DNA damage. DNA repair was characterized by genetic variants and functional activities of base and nucleotide excision repair pathways. Sex, fruit-based food consumption and XPG genotype were factors significantly associated with the level of DNA damage. DNA damage was higher in women (p=0.035). Fruit consumption was negatively associated with the number of all measured DNA lesions, and this effect was mediated mostly by β-cryptoxanthin and β-tocopherol (p<0.05). XPG 1104His homozygotes appeared more vulnerable to DNA damage accumulation (p=0.001). Sex and individual antioxidants were also associated with DNA repair capacity; both the base and nucleotide excision repairs were lower in women and the latter increased with higher plasma levels of ascorbic acid and α-carotene (p<0.05). We have determined genetic and dietary factors that modulate DNA integrity. We propose that the positive health effect of fruit intake is partially mediated via DNA damage suppression and a simultaneous increase in DNA repair capacity.

Keywords: DNA damage; DNA repair capacity; Diet; Genetic polymorphisms; Molecular epidemiology study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antioxidants / metabolism*
  • DNA Damage / genetics*
  • DNA Repair*
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Endonucleases / genetics*
  • Endonucleases / metabolism
  • Feeding Behavior*
  • Female
  • Gene-Environment Interaction
  • Genetic Markers
  • Genetic Variation
  • Humans
  • Male
  • Middle Aged
  • Norway
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Polymorphism, Single Nucleotide
  • Sex Factors
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Young Adult

Substances

  • Antioxidants
  • DNA excision repair protein ERCC-5
  • DNA-Binding Proteins
  • Genetic Markers
  • Nuclear Proteins
  • Transcription Factors
  • Endonucleases