E-cadherin and β-catenin expression during urothelial carcinogenesis induced by N-butyl-N-(4-hydroxybutyl) nitrosamine in mice

Urol Int. 2013;91(4):462-6. doi: 10.1159/000348329. Epub 2013 Mar 20.

Abstract

Background: E-cadherin and β-catenin are adhesion molecules that promote integrity and stability of the urothelium. A decrease in their expression is associated with more aggressive tumour phenotypes with the ability to invade and metastasize.

Material and methods: 45 ICR male mice were used, of which 25 received N-butyl-N-(4-hydroxybutyl)nitrosamine (0.05%) in drinking water for a period of 12 weeks. Immunohistochemical expression was evaluated in all urinary bladder preparations for E-cadherin and for β-catenin.

Results: Preneoplastic lesions showed staining patterns similar to normal urothelium. In simple and nodular hyperplasia, membrane staining was dominant (66.7-78.6 and 50-100%, respectively). In dysplasia a cytoplasmic pattern was prevalent (86.7-100%). Neoplastic lesions exhibit an abnormal staining pattern (100%) with heterogeneous staining (cytoplasmic, nuclear and membrane staining). A strong correlation was observed between both adhesion molecule staining patterns (r = 0.83; p = 0.039).

Conclusions: In mice, as in humans, E-cadherin and β-catenin are valuable tools to investigate cellular adhesion status of urothelium and can be considered as indicators of tumour aggressiveness and evolution.

MeSH terms

  • Animals
  • Butylhydroxybutylnitrosamine / chemistry*
  • Cadherins / metabolism*
  • Carcinogenesis
  • Cell Adhesion
  • Cytoplasm / metabolism
  • Disease Progression
  • Gene Expression Regulation, Neoplastic
  • Immunohistochemistry
  • Male
  • Mice
  • Mice, Inbred ICR
  • Phenotype
  • Prognosis
  • Urinary Bladder / drug effects
  • Urinary Bladder Neoplasms / chemically induced
  • Urinary Bladder Neoplasms / metabolism*
  • Urothelium / metabolism
  • beta Catenin / metabolism*

Substances

  • CTNNB1 protein, mouse
  • Cadherins
  • beta Catenin
  • Butylhydroxybutylnitrosamine