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1.
Exp Mol Pathol ; 103(3): 300-305, 2017 12.
Artigo em Inglês | MEDLINE | ID: mdl-29175302

RESUMO

Proteinases secreted by the prostate gland have a reproductive function in cleaving proteins in the ejaculate and in the female reproductive tract, but some may have a fundamental role in disease and pathological processes including cancer. The purpose of this study was to determine if there were differences in proteinase activities in urine samples collected following prostate massage of men positive (CaP) or negative (no evidence of malignancy, NEM) for biopsy determined prostate cancer. Matrix metalloproteinase (MMP) and serine proteinase activities were detected using protein substrate zymography. There were no differences in activities of MMP-2, proMMP-9, and MMP-9/NGAL (neutrophil gelatinase associated lipocalin) complex (gelatin substrate) in men with detected prostate cancer, although the latter two were somewhat diminished. A caseinolytic activity of about 75kDa inhibited by calcium did not differ between the NEM and CaP groups. Heparin stimulated calcium sensitive gelatinolytic activities of approximately 22, 42, and 60kDa, but did not affect activities of MMP-2, MMP-9, or the 75kDa caseinolytic activity. The 22, 42, and 60kDa activities appear to be serine proteinases since they were inhibited by benzamidine. There was a significant decrease in the 22kDa heparin-stimulated serine proteinase activity in urines of men with cancer. Proteinase expression and activities, perhaps in combination with other potential markers, may prove useful in urine for detection and evaluation of prostate cancer.


Assuntos
Biomarcadores Tumorais/urina , Metaloproteinase 2 da Matriz/urina , Metaloproteinase 9 da Matriz/urina , Neoplasias da Próstata/urina , Serina Proteases/urina , Idoso , Benzamidinas/administração & dosagem , Cálcio/metabolismo , Heparina/química , Humanos , Lipocalina-2/urina , Masculino , Pessoa de Meia-Idade , Neoplasias da Próstata/enzimologia , Neoplasias da Próstata/patologia
2.
J Urol ; 174(3): 1124-8, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16094078

RESUMO

PURPOSE: Dipeptidylpeptidase IV (DPIV) is a multifunctional type II plasma membrane glycoprotein with serine-type exopeptidase activity that is secreted by the prostate and increased in prostate cancer. We determined whether changes in DPIV activities in prostatic tissue zones and expressed secretions were associated with the presence of cancer. MATERIALS AND METHODS: Expressed prostatic secretion (EPS), and biopsy of the transition (TZ) and peripheral (PZ) zones were collected from men undergoing ultrasound guided prostate biopsy. DPIV activities were measured by glypro-p-nitroanalide hydrolysis. RESULTS: DPIV activities were significantly higher in TZ than in PZ tissues in men with no evidence of malignancy. However, activities in EPS were negatively associated with TZ volume and positively associated with PZ volume. Mean and median DPIV activities in EPS from men with biopsy determined cancer were significantly higher than in men with no evidence of malignancy. DPIV activities in TZ and PZ biopsies were higher in men with cancer but most markedly in the PZ. CONCLUSIONS: These data indicate that secreted DPIV originates from the TZ and PZ. Increased DPIV activities in cancer are strongly associated with the PZ, which is the zone most commonly involved with cancer. Measuring DPIV levels in expressed EPS or post-digital rectal prostate examination urine may be useful for evaluating men for prostate cancer.


Assuntos
Adenosina Desaminase/metabolismo , Biomarcadores Tumorais/metabolismo , Dipeptidil Peptidase 4/metabolismo , Glicoproteínas/metabolismo , Próstata/enzimologia , Neoplasias da Próstata/diagnóstico , Idoso , Biópsia/métodos , Endossonografia/métodos , Humanos , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Próstata/metabolismo , Próstata/patologia , Hiperplasia Prostática/diagnóstico , Hiperplasia Prostática/enzimologia , Hiperplasia Prostática/patologia , Neoplasias da Próstata/enzimologia , Neoplasias da Próstata/patologia
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