Smad4 haploinsufficiency in mouse models for intestinal cancer

Oncogene. 2006 Mar 23;25(13):1841-51. doi: 10.1038/sj.onc.1209226.

Abstract

The Smad4(+/E6sad) mouse carries a null mutation in the endogenous Smad4 gene resulting in serrated adenomas and mixed polyposis of the upper gastrointestinal (GI) tract with 100% penetrance. Here, we show by loss of heterozygosity (LOH) analysis and immunohistochemistry (IHC) that, although the majority of the tumors appear at 9 months of age, somatic loss of the wild-type Smad4 allele occurs only at later stages of tumor progression. Hence, haploinsufficiency underlies Smad4-driven tumor initiation in the GI tract. As both the Apc and Smad4 tumor suppressor genes map to mouse chromosome 18, we have bred Smad4(+/E6sad) with the Apc(+/1638N) model to generate two distinct compound heterozygous lines carrying both mutations either in cis (CAS) or in trans (TAS). Strikingly, both models show increased tumor multiplicities when compared with the single mutant littermates, although CAS mice are more severely affected and became moribund at only 5-6 weeks of age. Phenotypic and molecular analyses indicate that Smad4 haploinsufficiency is sufficient to significantly affect tumor initiation and progression both prior to and upon loss of Apc function. Moreover, complete loss of Smad4 strongly enhances Apc-driven tumor formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age of Onset
  • Animals
  • DNA Mutational Analysis
  • Disease Progression
  • Genes, APC*
  • Immunohistochemistry
  • Intestinal Neoplasms / genetics*
  • Intestinal Neoplasms / physiopathology
  • Loss of Heterozygosity*
  • Mice
  • Mice, Inbred C57BL
  • Phenotype
  • Signal Transduction
  • Smad4 Protein / genetics*
  • Transforming Growth Factor beta / physiology
  • Wnt Proteins / physiology

Substances

  • Smad4 Protein
  • Smad4 protein, mouse
  • Transforming Growth Factor beta
  • Wnt Proteins