Induction of DNA damage signaling genes in benzidine-treated HepG2 cells

Environ Mol Mutagen. 2011 Oct;52(8):664-72. doi: 10.1002/em.20669. Epub 2011 Aug 4.

Abstract

We examined genotoxicity and DNA damage response in HepG2 cells following exposure to benzidine. Using the Comet assay, we showed that benzidine (50-200 μM) induces DNA damage in HepG2 cells. DNA damage signaling pathway-based PCR arrays were used to investigate expression changes in genes involved in cell-cycle arrest, apoptosis, and DNA repair and showed upregulation of 23 genes and downregulation of one gene in benzidine-treated cells. Induction of G2/M arrest and apoptosis was confirmed at the protein level. Real-time PCR and Western blots were used to demonstrate the expression of select DNA repair-associated genes from the PCR array. Upregulation of the p53 protein in benzidine-treated cells suggests the induction of the p53 DNA damage signaling pathway. Collectively, DNA damage response genes induced by benzidine indicate recruitment complex molecular machinery involved in DNA repair, cell-cycle arrest, and potentially, activation of the apoptosis.

MeSH terms

  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Benzidines / toxicity*
  • Blotting, Western
  • Cell Cycle / drug effects
  • Cell Cycle / genetics
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Comet Assay
  • DNA Damage / genetics*
  • DNA Repair / genetics*
  • Down-Regulation
  • Gene Expression Profiling*
  • Hep G2 Cells
  • Humans
  • Mutagens / toxicity*
  • Real-Time Polymerase Chain Reaction
  • Tumor Suppressor Protein p53 / genetics*
  • Up-Regulation

Substances

  • Benzidines
  • Mutagens
  • Tumor Suppressor Protein p53
  • benzidine