Clinical significance of circulating endothelial adhesion molecules (sE-selectin and sICAM) in untreated multiple myeloma patients

Clin Chim Acta. 2004 Nov;349(1-2):39-43. doi: 10.1016/j.cccn.2004.05.025.

Abstract

Background: The expression of adhesion molecules is important for the interaction of myeloma cells with the bone marrow microenvironment. In the current study, serum soluble adhesion molecules (sICAM-1 and sE-selectin) were measured in untreated multiple myeloma (MM) patients in relation with other markers of disease activity.

Materials and methods: The study group consisted of 67 patients with MM (classified according to the Durie-Salmon classification) and 15 controls. Interleukin-6 (IL-6), sICAM-1 and sE-selectin concentrations were determined by enzyme-linked immunosorbent assay (ELISA). In addition, the monoclonal protein, erythrocyte sedimentation rate (ESR) and hemoglobin (Hb) concentration were also determined.

Results: Serum sICAM-1 level increased significantly at advanced stages of MM and was higher in comparison to controls (p<0.01). sE-selectin increased significantly with advancing stage of the disease, but did not differ from controls. IL-6, ESR and M-component were significantly higher and Hb concentrations lower with advancing stage of disease. There was a positive correlation of IL-6 with sICAM-1 and sE-selectin.

Conclusions: We conclude that serum sICAM-1 differs in multiple myeloma patients from normals and together with sE-selectin increase in parallel to increasing stage of disease, which may reflect a dysregulation and possible involvement of these adhesion molecules in myeloma progression.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers
  • Blood Sedimentation
  • E-Selectin / blood*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Hemoglobins / metabolism
  • Humans
  • Intercellular Adhesion Molecule-1 / blood*
  • Interleukin-6 / blood
  • Male
  • Middle Aged
  • Multiple Myeloma / blood*
  • Multiple Myeloma / therapy

Substances

  • Biomarkers
  • E-Selectin
  • Hemoglobins
  • Interleukin-6
  • Intercellular Adhesion Molecule-1