Literature DB >> 10024688

Elevation of urokinase-type plasminogen activator and its receptor densities as new predictors of disease progression and prognosis in men with prostate cancer.

H Miyake1, I Hara, K Yamanaka, S Arakawa, S Kamidono.   

Abstract

We examined whether two newly defined parameters, the density of urokinase-type plasminogen activator (uPAD) and the density of its receptor (uPARD), which were determined by dividing the serum levels of uPA and uPAR by the prostate volume, respectively, could be used as predictors of the progression and prognosis of prostate cancer (PC). Serum levels of uPA and uPAR in 40 healthy controls, 70 patients with benign prostatic hypertrophy (BPH) and 80 patients with PC were measured by a sandwich enzyme immunoassay, and prostate volume was measured by ultrasonography. The mean levels of uPAD and uPARD in patients with PC were significantly higher than those in healthy controls and patients with BPH. Furthermore, the uPAD and uPARD levels in PC patients with metastasis were significantly elevated compared with those in patients without metastasis. Among patients who underwent radical prostatectomy, the levels of uPAD and uPARD in patients with pathologically organ-confined disease were significantly lower than in those with advanced disease. The overall survival rate of PC cancer patients with elevated levels of either uPAD or uPARD, or of both, was significantly lower than that of patients with normal levels of uPAD and uPARD. In addition, Cox's multivariate analysis revealed that the elevation of uPAD or uPARD level, or of both, was strongly associated with overall survival in PC patients. These findings suggest that the elevation of uPAD or uPARD, or of both, could be used as new predictors of progression and prognosis in patients with PC.

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Year:  1999        PMID: 10024688     DOI: 10.3892/ijo.14.3.535

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  21 in total

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Journal:  Neoplasia       Date:  2004 May-Jun       Impact factor: 5.715

2.  The p75(NTR) metastasis suppressor inhibits urokinase plasminogen activator, matrix metalloproteinase-2 and matrix metalloproteinase-9 in PC-3 prostate cancer cells.

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Journal:  Clin Exp Metastasis       Date:  2006-08-16       Impact factor: 5.150

3.  Analysis of soluble urokinase plasminogen activator receptor in multiple myeloma for predicting prognosis.

Authors:  Jie Shen; Qing Wang; Juan Wang; Guo-Hong Su; Juan Wang; Sheng-Hu Guo; Y A Liu; Zheng Wu; Rong-Feng Liu; Xing Li; Xiao-Jin Guo; Jing Cao; Yue-Hua Zhang; Zhi-Yu Wang
Journal:  Oncol Lett       Date:  2015-08-14       Impact factor: 2.967

4.  Demethylation-linked activation of urokinase plasminogen activator is involved in progression of prostate cancer.

Authors:  Sai Murali Krishna Pulukuri; Norman Estes; Jitendra Patel; Jasti S Rao
Journal:  Cancer Res       Date:  2007-02-01       Impact factor: 12.701

5.  Maspin expression inhibits osteolysis, tumor growth, and angiogenesis in a model of prostate cancer bone metastasis.

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Journal:  Proc Natl Acad Sci U S A       Date:  2003-06-03       Impact factor: 11.205

6.  Inhibition of histone deacetylase activity promotes invasion of human cancer cells through activation of urokinase plasminogen activator.

Authors:  Sai Murali Krishna Pulukuri; Bharathi Gorantla; Jasti S Rao
Journal:  J Biol Chem       Date:  2007-10-08       Impact factor: 5.157

7.  First (18)F-labeled ligand for PET imaging of uPAR: in vivo studies in human prostate cancer xenografts.

Authors:  Morten Persson; Hongguang Liu; Jacob Madsen; Zhen Cheng; Andreas Kjaer
Journal:  Nucl Med Biol       Date:  2013-04-18       Impact factor: 2.408

8.  Isothiocyanate-Functionalized Bifunctional Chelates and fac-[M(I)(CO)3](+) (M = Re, (99m)Tc) Complexes for Targeting uPAR in Prostate Cancer.

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Journal:  Bioconjug Chem       Date:  2015-12-30       Impact factor: 4.774

9.  Small interfering RNA directed reversal of urokinase plasminogen activator demethylation inhibits prostate tumor growth and metastasis.

Authors:  Sai Murali Krishna Pulukuri; Jasti S Rao
Journal:  Cancer Res       Date:  2007-07-15       Impact factor: 12.701

10.  Cleaved high-molecular-weight kininogen and its domain 5 inhibit migration and invasion of human prostate cancer cells through the epidermal growth factor receptor pathway.

Authors:  Y Liu; R Pixley; M Fusaro; G Godoy; E Kim; M E Bromberg; R W Colman
Journal:  Oncogene       Date:  2009-06-01       Impact factor: 9.867

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