AFB1 hepatocarcinogenesis is via lipid peroxidation that inhibits DNA repair, sensitizes mutation susceptibility and induces aldehyde-DNA adducts at p53 mutational hotspot codon 249

Oncotarget. 2017 Mar 14;8(11):18213-18226. doi: 10.18632/oncotarget.15313.

Abstract

Aflatoxin B1 (AFB1) contamination in the food chain is a major cause of hepatocellular carcinoma (HCC). More than 60% of AFB1 related HCC carry p53 codon 249 mutations but the causal mechanism remains unclear. We found that 1) AFB1 induces two types of DNA adducts in human hepatocytes, AFB1-8,9-epoxide-deoxyguanosine (AFB1-E-dG) induced by AFB1-E and cyclic α-methyl-γ-hydroxy-1,N2-propano-dG (meth-OH-PdG) induced by lipid peroxidation generated acetaldehyde (Acet) and crotonaldehyde (Cro); 2) the level of meth-OH-PdG is >30 fold higher than the level of AFB1-E-dG; 3) AFB1, Acet, and Cro, but not AFB1-E, preferentially induce DNA damage at codon 249; 4) methylation at -CpG- sites enhances meth-OH-PdG formation at codon 249; and 5) repair of meth-OH-PdG at codon 249 is poor. AFB1, Acet, and Cro can also inhibit DNA repair and enhance hepatocyte mutational sensitivity. We propose that AFB1-induced lipid peroxidation generated aldehydes contribute greatly to hepatocarcinogenesis and that sequence specificity of meth-OH-PdG formation and repair shape the codon 249 mutational hotspot.

Keywords: AFB1-8,9-epoxide-deoxyguanosine; aflatoxin B1; cyclic α-methyl-γ-hydroxy-1,N2-propano-dG; hepatocellular carcinoma; p53 codon 249 mutations.

MeSH terms

  • Aflatoxin B1 / toxicity*
  • Aldehydes / metabolism*
  • Carcinoma, Hepatocellular / chemically induced
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / metabolism
  • Carcinoma, Hepatocellular / pathology
  • Codon / drug effects
  • DNA Adducts / biosynthesis*
  • DNA Repair / drug effects*
  • Genes, p53 / drug effects*
  • Hep G2 Cells
  • Humans
  • Lipid Peroxidation / drug effects
  • Liver Neoplasms / chemically induced*
  • Liver Neoplasms / genetics
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology
  • Mutation

Substances

  • Aldehydes
  • Codon
  • DNA Adducts
  • Aflatoxin B1