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Plasminogen activators and plasminogen activator inhibitors in human colorectal carcinoma tissues are not expressed by the tumour cells.

Abstract
Plasminogen activators (PA) have been implicated with the degradation of extracellular matrix during the invasive growth of metastasising tumour cells. The significance of PA expression in tumour cells for the in vivo growth of malignant tumours is still a matter of debate. We, therefore, performed immunohistological studies on human colon tumours using monoclonal antibodies against urokinase- (u-PA) and tissue-type plasminogen activator (t-PA) as well as against plasminogen activator inhibitors 1 and 2 (PAI-1, PAI-2). Normal colorectal mucosa of seven samples was negative for all four constituents of the PA system. Tumour epithelium of 64 colorectal carcinomas and 10 liver metastases was consistently negative for both, PA and their inhibitors. However, two of four human colon carcinoma cell lines weakly expressed u-PA, PAI-1 and PAI-2. Intestinal dendritic or fibroblast-like cells within the tumour tissue strongly expressed u-PA and, at a lower level, also t-PA, PAI-1 and PAI-2. Vascular endothelial cells were weakly positive for all components of the PA system in colon carcinoma. Our findings indicate that colon carcinoma cells in their natural environment do not express constituents of the PA system. PA activity, previously found in colon carcinoma tissue, is most likely derived from interstitial cells.
AuthorsK Koretz, P Möller, R Schwartz-Albiez
JournalEuropean journal of cancer (Oxford, England : 1990) (Eur J Cancer) Vol. 29A Issue 8 Pg. 1184-9 ( 1993) ISSN: 0959-8049 [Print] England
PMID8518031 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Plasminogen Inactivators
  • Plasminogen Activators
Topics
  • Colonic Neoplasms (chemistry)
  • Dendritic Cells (chemistry)
  • Humans
  • Intestinal Mucosa (chemistry)
  • Liver Neoplasms (secondary)
  • Plasminogen Activators (analysis)
  • Plasminogen Inactivators (analysis)
  • Rectal Neoplasms (chemistry)
  • Tumor Cells, Cultured (chemistry)

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