Oxidative DNA damage by hyperglycemia-related aldehydes and its marked enhancement by hydrogen peroxide

FEBS Lett. 2003 Nov 6;554(1-2):138-42. doi: 10.1016/s0014-5793(03)01129-3.

Abstract

Increased risks of cancers and oxidative DNA damage have been observed in diabetic patients. Many endogenous aldehydes such as 3-deoxyglucosone and glyceraldehyde (GA) increase under hyperglycemic conditions. We showed that these aldehydes induced Cu(II)-mediated DNA damage, including 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodG) formation. GA had the strongest ability to damage DNA, and addition of low concentrations of H2O2 markedly enhanced the DNA damage. GA significantly increased 8-oxodG formation in human cultured cells (HL-60), and H2O2 enhanced it. We conclude that oxidative DNA damage by hyperglycemia-related aldehydes, especially GA, and marked enhancement of DNA damage by H2O2 may participate in diabetes-associated carcinogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 8-Hydroxy-2'-Deoxyguanosine
  • Aldehydes / pharmacology*
  • Copper / pharmacology
  • DNA Damage*
  • Deoxyglucose / analogs & derivatives*
  • Deoxyglucose / pharmacology
  • Deoxyguanosine / analogs & derivatives*
  • Diabetes Complications
  • Drug Synergism
  • Glyceraldehyde / pharmacology
  • HL-60 Cells
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Hyperglycemia / metabolism*
  • Neoplasms / etiology
  • Oxidation-Reduction

Substances

  • Aldehydes
  • Glyceraldehyde
  • Copper
  • 8-Hydroxy-2'-Deoxyguanosine
  • Deoxyglucose
  • Hydrogen Peroxide
  • 3-deoxyglucosone
  • Deoxyguanosine