Constitutive expression of ErbB-2 in gallbladder epithelium results in development of adenocarcinoma

Cancer Res. 2001 Oct 1;61(19):6971-6.

Abstract

Overexpression of ErbB-2 in the basal layer of biliary tract epithelium led to the development of gallbladder adenocarcinoma in 100% of transgenic mice by 3 months of age. In addition, tumors developed in other parts of the biliary tree (e.g., cholangiocarcinoma). Adenocarcinoma of the gallbladder appeared to arise via a stepwise process involving hyperplasia, adenoma formation, and then adenocarcinoma formation. Increased ErbB-2/epidermal growth factor receptor heterodimer formation, activation of mitogen-activated protein kinase, and up-regulation of cyclooxygenase-2 levels (mRNA and protein) were observed in gallbladder epithelium of these mice. These mice represent a unique new animal model for studying biliary tract carcinogenesis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / metabolism*
  • Animals
  • Cyclooxygenase 2
  • Epithelium / metabolism
  • Epithelium / pathology
  • Epithelium / physiology
  • Female
  • Fluorescent Antibody Technique, Indirect
  • Gallbladder / metabolism*
  • Gallbladder / pathology
  • Gallbladder / physiology
  • Gallbladder Neoplasms / genetics
  • Gallbladder Neoplasms / metabolism*
  • Gene Expression
  • Genes, p53 / genetics
  • Genes, ras / genetics
  • Isoenzymes / biosynthesis
  • Isoenzymes / genetics
  • Male
  • Mice
  • Mice, Transgenic
  • Mitogen-Activated Protein Kinases / metabolism
  • Mutation
  • Phosphatidylinositol 3-Kinases / metabolism
  • Prostaglandin-Endoperoxide Synthases / biosynthesis
  • Prostaglandin-Endoperoxide Synthases / genetics
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptor, ErbB-2 / blood*
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / physiology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / physiology
  • Transgenes
  • src-Family Kinases / metabolism

Substances

  • Isoenzymes
  • RNA, Messenger
  • Cyclooxygenase 2
  • Prostaglandin-Endoperoxide Synthases
  • Phosphatidylinositol 3-Kinases
  • Receptor, ErbB-2
  • src-Family Kinases
  • Mitogen-Activated Protein Kinases