Ogg1 knockout-associated lung tumorigenesis and its suppression by Mth1 gene disruption

Cancer Res. 2003 Mar 1;63(5):902-5.

Abstract

Using Mth1 and Ogg1 knockout mice, we evaluated the roles of these enzymes to prevent tumorigenesis and the accumulation of 8-oxoguanine (8-oxoG) in DNA. We found that lung adenoma/carcinoma spontaneously developed in Ogg1 knockout mice approximately 1.5 years after birth in which 8-oxoG was found to accumulate in their genomes. The mean number of tumors/mouse was 0.71 for the Ogg1 knockout mice, which was five times higher than that observed in wild-type mice (0.14). Although the accumulation of 8-oxoG was also confirmed in the Ogg1, Mth1 double knockout mice, we found no tumor in the lungs of these mice. This observation suggests that Mth1 gene disruption resulted in a suppression of the tumorigenesis caused by an Ogg1 deficiency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / enzymology
  • Adenocarcinoma / genetics*
  • Animals
  • DNA Repair Enzymes*
  • DNA-Formamidopyrimidine Glycosylase
  • Female
  • Guanine / analogs & derivatives*
  • Guanine / metabolism
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / genetics*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • N-Glycosyl Hydrolases / genetics*
  • Pedigree
  • Phosphoric Monoester Hydrolases / genetics*

Substances

  • 8-hydroxyguanine
  • Guanine
  • Phosphoric Monoester Hydrolases
  • N-Glycosyl Hydrolases
  • DNA-Formamidopyrimidine Glycosylase
  • 8-oxodGTPase
  • DNA Repair Enzymes