Alkylation-induced colon tumorigenesis in mice deficient in the Mgmt and Msh6 proteins

Oncogene. 2009 Feb 5;28(5):734-41. doi: 10.1038/onc.2008.426. Epub 2008 Nov 24.

Abstract

O(6)-methylguanine DNA methyltransferase (MGMT) suppresses mutations and cell death that result from alkylation damage. MGMT expression is lost by epigenetic silencing in a variety of human cancers including nearly half of sporadic colorectal cancers, suggesting that this loss maybe causal. Using mice with a targeted disruption of the Mgmt gene, we tested whether Mgmt protects against azoxymethane (AOM)-induced colonic aberrant crypt foci (ACF), against AOM and dextran sulfate sodium (DSS)-induced colorectal adenomas and against spontaneous intestinal adenomas in Apc(Min) mice. We also examined the genetic interaction of the Mgmt null gene with a DNA mismatch repair null gene, namely Msh6. Both Mgmt and Msh6 independently suppress AOM-induced ACF, and combination of the two mutant alleles had a multiplicative effect. This synergism can be explained entirely by the suppression of alkylation-induced apoptosis when Msh6 is absent. In addition, following AOM+DSS treatment Mgmt protected against adenoma formation to the same degree as it protected against AOM-induced ACF formation. Finally, Mgmt deficiency did not affect spontaneous intestinal adenoma development in Apc(Min/+) mice, suggesting that Mgmt suppresses intestinal cancer associated with exogenous alkylating agents, and that endogenous alkylation does not contribute to the rapid tumor development seen in Apc(Min/+) mice.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alkylating Agents / toxicity
  • Alkylation / genetics
  • Alkylation / physiology*
  • Animals
  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Azoxymethane / toxicity
  • Carcinogens / toxicity
  • Carcinoma / genetics*
  • Carcinoma / metabolism*
  • Carcinoma / pathology
  • Colonic Neoplasms / chemically induced
  • Colonic Neoplasms / genetics*
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • DNA Modification Methylases / genetics*
  • DNA Repair Enzymes / genetics*
  • DNA-Binding Proteins / genetics*
  • Dextran Sulfate / toxicity
  • Genes, APC / physiology
  • Genetic Predisposition to Disease
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Tumor Suppressor Proteins / genetics*

Substances

  • Alkylating Agents
  • Carcinogens
  • DNA-Binding Proteins
  • Msh6 protein, mouse
  • Tumor Suppressor Proteins
  • Dextran Sulfate
  • DNA Modification Methylases
  • MGMT protein, mouse
  • DNA Repair Enzymes
  • Azoxymethane