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1.
Int. braz. j. urol ; 43(4): 638-643, July-Aug. 2017. tab
Article in English | LILACS | ID: biblio-892869

ABSTRACT

ABSTRACT Purpose To investigate the efficacy of signal peptide-CUB-EGF domain-containing protein 1 (SCUBE-1) as a novel biomarker of renal tumors. Materials and Methods 48 individuals were included in the study. The patient group (Group-1) consisted of 23 subjects diagnosed with renal tumor, and the control group (Group-2) of 25 healthy individuals. Patients diagnosed with renal tumor received surgical treatment consisting of radical or partial nephrectomy. Blood specimens were collected following overnight fasting. Signal peptide-CUB-EGF domain-containing protein 1 (SCUBE-1), soluble urokinase plasminogen activator receptor (suPAR) and carbonic anhydrase IX (CA IX) levels were measured from plasma samples. Patients in groups 1 and 2 were compared in terms of these biochemical parameters. Results The 23-member renal tumor group was made up of 17 (73.91%) male and 6 (26.08%) female patients with a mean age of 58.5±15.7 years (range 25 to 80). The 24-member healthy control group was made up of 16 (64%) male and 9 (36%) female subjects with a mean age of 52.4±9.12 years (range 40 to 67). Analysis revealed significant elevation in SCUBE-1 levels in the renal tumor group (p=0.005). No significant differences were detected between the groups with regard to CA IX or suPAR measurements (p=0.062 vs. p=0.176). Conclusions SCUBE-1 appears to represent a promising biomarker in the diagnosis and follow-up of patients with renal tumor.


Subject(s)
Humans , Male , Female , Adult , Aged , Aged, 80 and over , Carcinoma, Renal Cell/blood , Receptors, Urokinase Plasminogen Activator/blood , Carbonic Anhydrase IX/blood , Kidney Neoplasms/blood , Membrane Proteins/blood , Calcium-Binding Proteins , Carcinoma, Renal Cell/diagnosis , Biomarkers, Tumor/blood , Case-Control Studies , Kidney Neoplasms/diagnosis , Middle Aged
2.
Int. braz. j. urol ; 42(1): 146-153, Jan.-Feb. 2016. tab, graf
Article in English | LILACS | ID: lil-777330

ABSTRACT

ABSTRACT Purpose To investigate the protective effects against ischemia reperfusion injury of dipyridamole in a model of induced priapism in rats. Materials and Methods Twenty-four male Sprague-Dawley rats were divided into four groups, control, P/R, P/R+DMSO and P/R+D. 3ml blood specimens were collected from vena cava inferior in order to determine serum MDA, IMA, TAS, TOS and OSI values, and penile tissue was taken for histopathological examination in control group. Priapism was induced in P/R group. After 1h, priapism was concluded and 30 min reperfusion was performed. In P/R+DMSO group 1ml/kg DMSO was administered intraperitoneally 30 min before reperfusion, while in P/R+D group 10mg/kg dipyridamole was administered intraperitoneally 30 min before reperfusion. Blood and penis specimens were collected after the end of 30 min reperfusion period. Sinusoidal area (µm2), tears in tunica albuginea and injury parameters in sinusoidal endothelium of penis were investigated. Results Histopathological examination revealed no significant changes in term of sinusoidal area. A decrease in tears was observed in P/R+D group compared to P/R group (p<0.05). Endothelial injury decreased in P/R+D group compared to P/R group (p>0.05). There were no significant differences in MDA and IMA values between groups. A significant increase in TOS and OSI values was observed in P/R+D group compared to P/R group. A significant decrease in TAS levels was observed in P/R+D group compared to the P/R group. Conclusions The administration of dipyridamole before reperfusion in ischemic priapism model has a potential protective effect against histopathological injury of the penis.


Subject(s)
Animals , Male , Penis/blood supply , Priapism/prevention & control , Vasodilator Agents/pharmacology , Reperfusion Injury/prevention & control , Dipyridamole/pharmacology , Ischemia/prevention & control , Penis/pathology , Priapism/pathology , Time Factors , Penile Erection/drug effects , Serum Albumin , Biomarkers/blood , Random Allocation , Reproducibility of Results , Treatment Outcome , Oxidants/blood , Rats, Sprague-Dawley , Oxidative Stress , Ischemic Preconditioning/methods , Disease Models, Animal , Serum Albumin, Human , Malondialdehyde/blood , Antioxidants/analysis
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