Increased risk of oral cancer in diabetic animals is not associated with c-jun activation pathway

J Craniomaxillofac Surg. 2007 Dec;35(8):382-7. doi: 10.1016/j.jcms.2007.05.006. Epub 2007 Nov 26.

Abstract

Purpose: The expression of oncogenic protein c-jun was investigated in an experimental model of chemically induced carcinogenesis in normal and diabetic (type I) Sprague-Dawley rats.

Material and methods: Thirteen diabetic and twelve normal rats developed cancer after 4-nitroquinoline-N-oxide treatment, while six diabetic and six normal animals were used as controls. The biopsies were classified pathologically from oral mucosal dysplasia to moderately differentiated oral squamous cell carcinoma (OSCC) and studied immunohistochemically using monoclonal antibody against c-jun protein.

Results: Higher c-jun levels were observed in non-cancerous and precancerous stages of normal rats compared with diabetic rats, while in different tumour stages, the expression of c-jun was practically identical for both groups.

Conclusion: It seems that diabetes does not affect the c-jun N-terminal kinase (JNK)/c-jun pathway.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4-Nitroquinoline-1-oxide / adverse effects
  • Animals
  • Biopsy
  • Carcinogens
  • Carcinoma, Squamous Cell / chemically induced
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / pathology
  • Diabetes Mellitus, Experimental / complications*
  • Diabetes Mellitus, Experimental / genetics
  • Female
  • Gene Expression Regulation, Enzymologic / genetics
  • Gene Expression Regulation, Neoplastic / genetics
  • Immunohistochemistry
  • JNK Mitogen-Activated Protein Kinases / genetics
  • Mouth Mucosa / drug effects
  • Mouth Mucosa / pathology
  • Mouth Neoplasms / chemically induced*
  • Mouth Neoplasms / genetics
  • Mouth Neoplasms / pathology
  • Neoplasm Staging
  • Precancerous Conditions / chemically induced
  • Precancerous Conditions / genetics
  • Precancerous Conditions / pathology
  • Proto-Oncogene Proteins c-jun / genetics*
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Risk Factors

Substances

  • Carcinogens
  • Proto-Oncogene Proteins c-jun
  • 4-Nitroquinoline-1-oxide
  • JNK Mitogen-Activated Protein Kinases