The hamster cheek pouch carcinogenesis model

Irma B. Gimenez‐Conti, Thomas J. Slaga

Research output: Contribution to journalArticlepeer-review

136 Scopus citations

Abstract

The Syrian golden hamster cheek pouch carcinogenesis model is probably the best‐known animal system that closely compares to events involved in the development of premalignant and malignant human oral cancers. Furthermore, it is one of the most well‐characterized models for squamous cell carcinomas (SCCs). However, stages of carcinogenesis (initiation, promotion, and progression) have not been well‐defined in this system. Basic understanding of the mechanism(s) of carcinogenesis in this organ is instrumental for the development of new strategies for chemoprevention and early chemointervention. To understand the important early events that occur in the hamster cheek pouch carcinogenesis model, we compared it to the mouse skin model, where a number of critical events have been well characterized. We determined that approximately 60% of the hamster cheek pouch SCCs have a mutation in codon 61 of the Ha‐ras gene. We also established a two‐stage carcinogenesis protocol in this model using a single dose of dimethylbenz(a)anthracene (DMBA) and multiple doses of benzoyl peroxide for 45 weeks. Twenty‐five percent of tumors developed with this protocol had the same mutation in codon 61 of the Ha‐ras gene, confirming that this mutation, as in the mouse skin model, is initiation‐related. We examined the sequential expression of hyperplasia, micronucleated cells, ornithine decarboxylase (ODC) activity, polyamine levels, transglutaminase I activity, epidermal growth factor receptor (EGF‐R) levels, keratins, γ‐glutamyltranspeptidase (GGT), transforming growth factor ‐β1 (TGF‐β1), leukoplakia, and carcinomas induced during carcinogenesis. A number of these important biological molecular and genetic markers could be excellent intermediate endpoints in assessing the effects of various chemopreventive agents to be tested in the hamster cheek pouch model and in human clinical trials.

Original languageEnglish (US)
Pages (from-to)83-90
Number of pages8
JournalJournal of Cellular Biochemistry
Volume53
Issue numberS17F
DOIs
StatePublished - 1993
Externally publishedYes

Keywords

  • biological
  • buccal pouch
  • chemoprevention
  • genetic changes
  • hamster
  • intermediate biomarkers
  • molecular

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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