Differential expression patterns of S100A2, S100A4 and S100A6 during progression of human malignant melanoma

Int J Cancer. 1997 Aug 22;74(4):464-9. doi: 10.1002/(sici)1097-0215(19970822)74:4<464::aid-ijc19>3.0.co;2-9.


Three members of the S100 gene family, S100A2, S100A4 and S100A6, have been suggested to be associated with cancer development and metastasis. To study their involvement in the tumorigenesis of human melanoma, we examined the mRNA expression levels of the 3 genes in 45 melanoma metastases and in 20 benign nevi. Interestingly, whereas none of the metastases expressed S100A2 mRNA, and the expression level was low in 6 cell lines established from primary melanomas, all nevi showed moderate to high expression levels. Our results suggest that loss of S100A2 gene expression may be an early event in melanoma development. A significant correlation was found between the expression of S100A6 in melanoma metastases and both the survival time of the patients and the thickness of the corresponding primary tumors. For the S100A4 gene, however, no relationship was found between gene expression and clinical parameters of melanoma malignancy. The observed differences in expression patterns of the 3 S100 genes suggest distinct roles of their products in melanoma tumorigenesis and/or metastasis, and the results encourage studies to evaluate the potential value of using S100A2 and S100A6 expression levels as markers in the clinical management of melanoma.

Publication types

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

MeSH terms

  • Blotting, Southern
  • Calcium-Binding Proteins / analysis
  • Calcium-Binding Proteins / biosynthesis*
  • Cell Line
  • Disease Progression
  • Disease-Free Survival
  • Female
  • Humans
  • Melanoma / genetics
  • Melanoma / metabolism
  • Melanoma / mortality
  • Melanoma / pathology*
  • Multigene Family
  • Neoplasm Metastasis
  • Predictive Value of Tests
  • RNA, Messenger / biosynthesis
  • Skin Neoplasms / genetics
  • Skin Neoplasms / metabolism
  • Skin Neoplasms / mortality
  • Skin Neoplasms / pathology*
  • Statistics, Nonparametric
  • Survival Rate
  • Transcription, Genetic*
  • Tumor Cells, Cultured


  • Calcium-Binding Proteins
  • RNA, Messenger