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Purpose: To assess whether preoperative plasma levels of urokinase-type plasminogen activator (uPA) and its soluble receptor (uPAR) would predict cancer of the prostate (CaP) presence, stage, and prognosis.
Patients And Methods: Plasma levels of uPA and uPAR were measured in patients who underwent radical prostatectomy for clinically localized CaP (preoperative, n = 429; postoperative, n = 76), 44 healthy men, 19 patients with metastases to regional lymph nodes, and 10 patients with bone metastases.
Results: uPA and uPAR levels were significantly elevated in patients with CaP compared with healthy men and significantly declined after prostate removal. In CaP patients, uPA and uPAR levels both increased significantly from patients with nonmetastatic CaP to patients with lymph node metastases to patients with skeletal metastases. On univariate analysis, preoperative uPA and uPAR levels were significantly elevated in patients with extracapsular extension, seminal vesicle involvement, higher prostatectomy Gleason sum, lymph node invasion, lymphovascular invasion, perineural invasion, and higher tumor volume. Higher preoperative uPAR was associated with biochemical progression in univariate analysis. Conversely, higher preoperative uPA was independently associated with biochemical progression in preoperative or postoperative multivariate models. In patients with biochemical progression, preoperative uPA and uPAR were both significantly associated with shorter postprogression total serum prostate-specific antigen doubling times, failure to respond to salvage local radiation therapy, and/or development of distant metastasis.
Conclusion: Elevation of plasma uPA and uPAR levels in CaP patients seems to be partly caused by local release from the prostate. Plasma levels of uPA and uPAR are associated with features of biologically aggressive CaP, disease progression after radical prostatectomy, and metastasis.
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http://dx.doi.org/10.1200/JCO.2006.05.6853 | DOI Listing |
Arterioscler Thromb Vasc Biol
September 2025
Division of Hematology, Department of Medicine, UNC Blood Research Center, University of North Carolina at Chapel Hill.
The primary role of the fibrinolytic system is to degrade fibrin clots. However, the fibrinolytic system is often activated in patients with cancer and may affect cancer progression, metastasis, and patient survival. Clinical studies have shown that elevated plasma levels of uPA (urokinase plasminogen activator) are associated with cancer progression in patients with prostate and cervical cancers, whereas high plasma levels of soluble uPAR (uPA receptor) are associated with progression and metastasis in prostate, breast, bladder, and colorectal cancers.
View Article and Find Full Text PDFBiomed J
August 2025
Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan. Electronic address:
Plasminogen activator inhibitor-1 (PAI-1), a key regulator of the fibrinolytic system, has emerged as a multifaceted contributor to the pathogenesis of systemic sclerosis (SSc). Beyond its classical role in inhibiting plasminogen activation, PAI-1 is implicated in the dysregulation of vascular remodeling, promotion of fibrosis, modulation of immune responses, and the maintenance of cellular senescence-all of which are hallmarks of SSc. Notably, elevated PAI-1 expression has been observed in both patient-derived tissues and experimental models of the disease.
View Article and Find Full Text PDFInvest Ophthalmol Vis Sci
August 2025
Department of Biology, University of Pisa, Pisa, Italy.
Purpose: Retinitis pigmentosa (RP) is characterized by primary rod degeneration followed by secondary cone death. The urokinase-type plasminogen activator (uPA) and its cognate receptor (uPAR) have been recently suggested to regulate pro-inflammatory events in RP possibly through the interaction of uPAR with its lateral partners, including formyl peptide receptors (FPRs). This study explored whether the inhibition of the crosstalk between uPAR and FPR1 may counteract photoreceptor degeneration in the rd10 mouse model of RP.
View Article and Find Full Text PDFBioorg Chem
August 2025
College of Chemistry, Fuzhou University, 350116 Fuzhou, China; College of Biological and Pharmaceutical Engineering, Jilin Agricultural Science and Technology University, 132101 Jilin, China. Electronic address:
Cancer is characterized by the uncontrolled proliferation of cells that can invade and metastasize to distant organs, with metastasis accounting for over 90 % of cancer-related mortalities. The urokinase-type plasminogen activator receptor (uPAR), a critical hub for cancer proliferation and metastasis, angiogenesis, and inflammation, emerges as a promising anti-cancer and anti-metastasis target. Developing small-molecule inhibitors that disrupt the interaction between uPAR and its ligand, urokinase-type plasminogen activator (uPA), constitutes a major focus in anticancer drug discovery.
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