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Coordinate up-regulation of Sp1 DNA-binding activity and urokinase receptor expression in breast carcinoma.

Abstract
The regulatory mechanisms underlying the overexpression of urokinase-type plasminogen activator (uPA) and its receptor (uPAR) in highly invasive breast carcinomas remain poorly understood. In this study, we have simultaneously determined the level of uPAR and the activity of the transcription factor Sp1 in 14 breast carcinomas and 5 benign lesions. We found that uPAR levels and Sp1-binding activity are coordinately elevated in malignant tumors (r, 0.94; P < 0.001). On the contrary, undetectable or only barely detectable levels of uPAR and Sp1 activity were found in benign breast lesions. Finally, the engagement of uPAR by catalytically inactive uPA in the MDA-MB-231 breast carcinoma cell line results in a rapid up-regulation of Sp1-binding activity followed by an increase of uPAR protein. These results, taken together, suggest the existence of a uPA-dependent positive regulatory loop that may progressively enhance malignant breast cell invasiveness.
AuthorsA Zannetti, S Del Vecchio, M V Carriero, R Fonti, P Franco, G Botti, G D'Aiuto, M P Stoppelli, M Salvatore
JournalCancer research (Cancer Res) Vol. 60 Issue 6 Pg. 1546-51 (Mar 15 2000) ISSN: 0008-5472 [Print] United States
PMID10749121 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • DNA-Binding Proteins
  • Oligonucleotides
  • PLAUR protein, human
  • Receptors, Cell Surface
  • Receptors, Urokinase Plasminogen Activator
  • Sp1 Transcription Factor
  • Urokinase-Type Plasminogen Activator
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Blotting, Western
  • Breast (chemistry, pathology)
  • Breast Neoplasms (metabolism, pathology)
  • DNA-Binding Proteins (metabolism)
  • Female
  • HeLa Cells
  • Humans
  • Immunohistochemistry
  • Middle Aged
  • Oligonucleotides (metabolism)
  • Protein Binding
  • Receptors, Cell Surface (biosynthesis)
  • Receptors, Urokinase Plasminogen Activator
  • Sp1 Transcription Factor (metabolism)
  • Tumor Cells, Cultured (drug effects, metabolism)
  • Up-Regulation (drug effects)
  • Urokinase-Type Plasminogen Activator (pharmacology)

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