Fas and Fas ligand: expression and soluble circulating levels in cutaneous malignant melanoma

Br J Dermatol. 2002 Jul;147(1):80-6. doi: 10.1046/j.1365-2133.2002.04745.x.

Abstract

Background: The Fas/Fas ligand (FasL) system plays a key part in maintaining tissue homeostasis via the induction of apoptosis. Functional impairment of the Fas/FasL system is associated with the development and progression of malignancies. Malignant melanoma cells and tissues have been shown to express Fas and FasL to variable extents.

Objectives: To demonstrate the expression and the presence of soluble circulating levels of Fas and FasL in cutaneous malignant melanoma.

Methods: Biopsy specimens of 42 patients with primary melanoma and nine patients with cutaneous metastatic melanoma were obtained for immunohistochemistry studies. All patients were followed for at least 5 years. In another 46 patients with melanoma (15 stage I and II; 11 stage III; and 20 stage IV) and in 10 healthy volunteer control subjects circulating levels of Fas and FasL were analysed with commercial ELISA tests.

Results: FasL was strongly positive in 38 (90%) of 42 primary melanomas; two of nine metastases did not express FasL. In the primary melanomas Fas was strongly or intensely positive in 17 (40%), moderately or weakly positive in 10 (24%) and negative in 15 (36%) of 42 melanomas. Soluble Fas plasma levels in patients with metastatic malignant melanoma were significantly elevated over those in the control group (P = 0.01).

Conclusions: The absence of Fas in most of the thick melanomas that did not metastasize, and in insitu melanomas, might be taken as a theoretical factor for a good prognosis. Soluble Fas is increased in patients with metastatic melanoma and might be associated with poor prognosis.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / analysis*
  • Biomarkers, Tumor / blood
  • Enzyme-Linked Immunosorbent Assay
  • Fas Ligand Protein
  • Female
  • Humans
  • Ligands
  • Male
  • Melanoma / blood
  • Melanoma / chemistry*
  • Melanoma / secondary
  • Membrane Glycoproteins / analysis*
  • Membrane Glycoproteins / blood
  • Middle Aged
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / blood
  • Neoplasm Staging
  • Skin Neoplasms / blood
  • Skin Neoplasms / chemistry*
  • Skin Neoplasms / pathology
  • Solubility
  • fas Receptor / analysis*
  • fas Receptor / blood

Substances

  • Biomarkers, Tumor
  • FASLG protein, human
  • Fas Ligand Protein
  • Ligands
  • Membrane Glycoproteins
  • Neoplasm Proteins
  • fas Receptor