Apc deficiency predisposes to renal carcinoma in the mouse

Oncogene. 2005 Dec 8;24(55):8205-10. doi: 10.1038/sj.onc.1208956.

Abstract

Deregulation of Wnt signalling has recently been implicated in human renal cancer. Here, we directly test this association by using a Cre-LoxP strategy to inactivate the Adenomatous Polyposis Coli (Apc) gene in the murine renal epithelium. Mice homozygous for a conditional Apc allele were intercrossed with mice transgenic for Cre recombinase under control of the Cyp1A promoter, which delivers constitutive recombination within a proportion of cells in the renal epithelium. Inactivation of Apc leads to the accumulation of nuclear beta-catenin and the rapid development of multiple dysplastic foci. Renal carcinoma was observed with an earliest onset of 4 months. This predisposition was accelerated by p53 deficiency, reducing the earliest onset to 2 months. Compared to other murine models of kidney neoplasia, this represents particularly rapid onset of disease, and so implicates an important role for Apc in suppressing renal carcinoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Gene Deletion*
  • Genes, APC*
  • Homozygote
  • Integrases / genetics
  • Integrases / metabolism
  • Kidney Neoplasms / genetics*
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Tumor Suppressor Protein p53 / deficiency
  • Tumor Suppressor Protein p53 / genetics
  • Urothelium / pathology
  • Urothelium / physiology

Substances

  • Tumor Suppressor Protein p53
  • Cre recombinase
  • Integrases