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Intercellular adhesion molecule-3 on endothelial cells. Expression in tumors but not in inflammatory responses.

Abstract
Intercellular adhesion molecule-3 (ICAM-3) was identified as the third counter-receptor for lymphocyte function-associated antigen-1. ICAM-3 is absent on endothelial cells in normal tissues but found on endothelial cells in lymphomas. Here, we examined ICAM-3 expression on vascular endothelial cells in lymphomas, nonlymphoid malignancies, benign tumors, and inflammatory diseases. We compared the expression of ICAM-3 on endothelial cells with the severity of inflammatory infiltrates and with the presence of E-selectin and VCAM-1. We found that ICAM-3 expression on endothelial cells was high on both benign and malignant tumors whereas it was low in inflammatory diseases. In contrast to E-selectin, ICAM-3 expression on endothelial cells was not correlated to the severity of inflammatory infiltrates. In hemangiomas, we showed by Northern blot analysis and immunocytochemistry that ICAM-3 expression was induced and that it was localized in immature areas that sustain the early stages of angiogenesis. Therefore, expression of ICAM-3 on blood vessels does not seem to play a role in the recruitment of leukocytes during inflammation but rather is correlated with angiogenesis and tumor development.
AuthorsN Patey, R Vazeux, D Canioni, T Potter, W M Gallatin, N Brousse
JournalThe American journal of pathology (Am J Pathol) Vol. 148 Issue 2 Pg. 465-72 (Feb 1996) ISSN: 0002-9440 [Print] United States
PMID8579109 (Publication Type: Journal Article)
Chemical References
  • Antigens, CD
  • Antigens, Differentiation
  • Biomarkers, Tumor
  • Cell Adhesion Molecules
  • E-Selectin
  • ICAM3 protein, human
  • Vascular Cell Adhesion Molecule-1
Topics
  • Antigens, CD
  • Antigens, Differentiation
  • Biomarkers, Tumor
  • Blotting, Northern
  • Cell Adhesion Molecules (analysis, biosynthesis)
  • E-Selectin (analysis, biosynthesis)
  • Endothelium, Vascular (cytology, metabolism)
  • Hemangioma (chemistry, metabolism)
  • Hodgkin Disease (metabolism)
  • Humans
  • Immunoenzyme Techniques
  • Inflammation (metabolism)
  • Lymphoid Tissue (metabolism)
  • Lymphoma (chemistry, metabolism)
  • Lymphoma, Non-Hodgkin (metabolism)
  • Neoplasms (metabolism)
  • Neovascularization, Pathologic (physiopathology)
  • Vascular Cell Adhesion Molecule-1 (analysis, biosynthesis)

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