Differential expression of c-jun and c-fos mRNAs in squamous cell carcinoma of the head and neck: associations with uPA, gelatinase B, and matrilysin mRNAs

Head Neck. 2002 Jan;24(1):24-32. doi: 10.1002/hed.10009.

Abstract

Background: Head and neck squamous cell carcinomas (HNSCC) are known for their invasive behavior. The invasiveness of these tumors requires proteases, some of which as urokinase-type plasminogen activator (uPA), gelatinase B and matrilysin are regulated through AP-1 dependent transcriptional mechanisms. AP-1 consists of several proteins, including those encoded by the proto-oncogenes c-jun and c-fos. The aim of this study was to: first, evaluate the expression levels of matrix metalloproteases (matrilysin and gelatinase B) and uPA mRNAs; second, examine whether these genes might be associated with c-jun and c-fos expression; third, examine the relationship between the expression of these genes and HNSCC clinico-pathological features.

Methods: We have analyzed 38 HNSCC primary tumors and matched mucosa tissues for uPA, gelatinase B, matrilysin, c-fos, and c-jun by Northern-blot analysis.

Results: uPA, gelatinase B, matrilysin, and c-jun mean levels were statistically higher in the tumors than in the normal adjacent mucosa, whereas no difference was found when c-fos mRNA values were compared, c-jun mRNA expression correlated directly with gelatinase B and matrilysin mRNA levels, but no association with uPA mRNA was observed, c-fos mRNA levels were not associated with the tested proteases, but low levels were determined in tumors from older patients who subsequently developed a 2(nd) tumor. No evidence of correlation between expression of uPA, matrilysin, and c-jun in tumors and clinico-pathological features was found. Gelatinase B mRNA high levels were associated to presence of cervical recurrences.

Conclusion: Expression of c-jun seems to be involved in the regulation of gelatinase B and matrilysin being not related to uPA. Lack of association with c-fos may indicate that other fos family members might play a role in the transcriptional activity of the analyzed proteases in HNSCC tumors.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / analysis*
  • Biopsy, Needle
  • Blotting, Northern
  • Carcinoma, Squamous Cell / chemistry*
  • Carcinoma, Squamous Cell / pathology
  • Culture Techniques
  • Female
  • Gene Expression Regulation, Neoplastic
  • Head and Neck Neoplasms / chemistry*
  • Head and Neck Neoplasms / pathology
  • Humans
  • Matrix Metalloproteinase 7 / genetics
  • Matrix Metalloproteinase 9 / genetics
  • Middle Aged
  • Neoplasm Invasiveness
  • Proto-Oncogene Proteins c-fos / genetics*
  • Proto-Oncogene Proteins c-jun / genetics*
  • RNA, Messenger / analysis*
  • RNA, Neoplasm / analysis*
  • Sensitivity and Specificity
  • Statistics, Nonparametric
  • Urokinase-Type Plasminogen Activator / genetics

Substances

  • Biomarkers, Tumor
  • Proto-Oncogene Proteins c-fos
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • RNA, Neoplasm
  • Urokinase-Type Plasminogen Activator
  • Matrix Metalloproteinase 7
  • Matrix Metalloproteinase 9