Literature DB >> 14754404

The urokinase plasminogen activator system: role in malignancy.

Michael J Duffy1.   

Abstract

The urokinase plasminogen activator (uPA) system consists of the serine protease uPA, its glycolipid-anchored receptor, uPAR and its 2 serpin inhibitors, plasminogen activator inhibitor-1 (PAI-1) and plasminogen activator inhibitor-2 (PAI-2). Recent findings suggest that the uPA system is causally involved at multiple steps in cancer progression. In particular, uPA has been implicated in remodelling of the extracellular matrix, enhancing both cell proliferation and migration and modulating cell adhesion. Consistent with its role in cancer progression, multiple groups have shown that high levels of uPA in primary breast cancers are independently associated with adverse outcome. Paradoxically, high levels of PAI-1 also correlate with poor prognosis in patients with breast cancer. The prognostic value of uPA/PAI-1 in axillary node-negative breast cancer patients was recently validated using both a prospective randomised trial and a pooled analysis, i.e., in 2 different Level 1 Evidence studies. Assay of uPA and PAI-1 may thus help identify low risk node-negative patients for whom adjuvant chemotherapy is unnecessary. Finally, preclinical studies show that either inhibition of uPA catalytic activity or prevention of uPA binding to its receptor reduces tumor growth, angiogenesis and metastasis.

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Year:  2004        PMID: 14754404     DOI: 10.2174/1381612043453559

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  120 in total

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3.  Plasminogen activation/plasmin in rheumatoid arthritis: matrix degradation and more.

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4.  Heparanase stimulation of protease expression implicates it as a master regulator of the aggressive tumor phenotype in myeloma.

Authors:  Anurag Purushothaman; Ligong Chen; Yang Yang; Ralph D Sanderson
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5.  Transformation by oncogenic Ras expands the early genomic response to transforming growth factor beta in intestinal epithelial cells.

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Review 6.  Tumor stroma as targets for cancer therapy.

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Review 7.  FERM control of FAK function: implications for cancer therapy.

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Journal:  Cell Cycle       Date:  2008-05-29       Impact factor: 4.534

8.  Increased expression of urokinase plasminogen activator and its cognate receptor in human seminomas.

Authors:  Salvatore Ulisse; Enke Baldini; Marcella Mottolese; Steno Sentinelli; Patrizia Gargiulo; Brancato Valentina; Salvatore Sorrenti; Anna Di Benedetto; Enrico De Antoni; Massimino D'Armiento
Journal:  BMC Cancer       Date:  2010-04-19       Impact factor: 4.430

9.  Increasing the relative expression of endogenous non-coding Steroid Receptor RNA Activator (SRA) in human breast cancer cells using modified oligonucleotides.

Authors:  Charlton Cooper; Jimin Guo; Yi Yan; Shilpa Chooniedass-Kothari; Florent Hube; Mohammad K Hamedani; Leigh C Murphy; Yvonne Myal; Etienne Leygue
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10.  Obesity and breast cancer: the roles of peroxisome proliferator-activated receptor-γ and plasminogen activator inhibitor-1.

Authors:  Jennifer C Carter; Frank C Church
Journal:  PPAR Res       Date:  2009-08-06       Impact factor: 4.964

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