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Tumour-expressed CD43 (sialophorin) mediates tumourmesothelial cell adhesion.

Abstract
Mesothelial cell intercellular adhesion molecule-1 (ICAM-1) has recently been shown to play a role in tumour cell adherence to the peritoneum. However, solid tumours poorly express its most ubiquitous ligand, beta2 integrin. The aim of this study was to investigate the role of the beta2 integrin subunit and CD43, a known ligand for ICAM-1, in the development of peritoneal metastases. beta2 Integrin subunit and CD43 expression was assessed on a number of tumour cell lines. Adhesion of SW1222 and PSN-1 cells to human peritoneal mesothelial cells was investigated using a fluorometric assay incorporating an inhibitory antibody to beta2 integrin and CD43. beta2 Integrin expression was not inducible on these tumour cell lines, but Western blotting demonstrated CD43 expression in all the cancer cell lines examined and cell surface expression was confirmed by flow cytometry. The anti-CD43 antibody significantly reduced adhesion of PSN-1 and SW1222 cells to HPMC, however beta2 integrin inhibition did not reduce tumour cell adhesion. CD43 is expressed by a variety of carcinoma cell lines, and plays a role in tumour cell-peritoneal adhesion probably via interactions with its putative ligand ICAM-1.
AuthorsPaul Ziprin, Nawar A Alkhamesi, Paul F Ridgway, David H Peck, Ara W Darzi
JournalBiological chemistry (Biol Chem) Vol. 385 Issue 8 Pg. 755-61 (Aug 2004) ISSN: 1431-6730 [Print] Germany
PMID15449712 (Publication Type: Journal Article)
Chemical References
  • Antigens, CD
  • CD18 Antigens
  • Indicators and Reagents
  • Leukosialin
  • SPN protein, human
  • Sialoglycoproteins
  • Intercellular Adhesion Molecule-1
Topics
  • Antigens, CD (biosynthesis, physiology)
  • Blotting, Western
  • CD18 Antigens (metabolism)
  • Cell Adhesion (physiology)
  • Cell Line, Tumor
  • Cells, Cultured
  • Epithelial Cells (metabolism)
  • Epithelium
  • Flow Cytometry
  • Humans
  • Indicators and Reagents
  • Intercellular Adhesion Molecule-1 (metabolism)
  • Leukosialin
  • Sialoglycoproteins (biosynthesis, physiology)

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