Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add filters








Language
Year range
1.
Asian Journal of Andrology ; (6): 324-329, 2018.
Article in English | WPRIM | ID: wpr-1009580

ABSTRACT

This study was performed to evaluate prostate-specific antigen-age volume (PSA-AV) scores in predicting prostate cancer (PCa) in a Chinese biopsy population. A total of 2355 men who underwent initial prostate biopsy from January 2006 to November 2015 in Huashan Hospital were recruited in the current study. The PSA-AV scores were calculated and assessed together with PSA and PSA density (PSAD) retrospectively. Among 2133 patients included in the analysis, 947 (44.4%) were diagnosed with PCa. The mean age, PSA, and positive rates of digital rectal examination result and transrectal ultrasound result were statistically higher in men diagnosed with PCa (all P < 0.05). The values of area under the receiver operating characteristic curves (AUCs) of PSAD and PSA-AV were 0.864 and 0.851, respectively, in predicting PCa in the entire population, both performed better than PSA (AUC = 0.805; P < 0.05). The superiority of PSAD and PSA-AV was more obvious in subgroup with PSA ranging from 2.0 ng ml-1 to 20.0 ng ml-1. A PSA-AV score of 400 had a sensitivity and specificity of 93.7% and 40.0%, respectively. In conclusion, the PSA-AV score performed equally with PSAD and was better than PSA in predicting PCa. This indicated that PSA-AV score could be a useful tool for predicting PCa in Chinese population.


Subject(s)
Aged , Aged, 80 and over , Humans , Male , Aging/pathology , Area Under Curve , Asian People , Digital Rectal Examination , Image-Guided Biopsy , Predictive Value of Tests , Prostate-Specific Antigen/blood , Prostatic Neoplasms/diagnostic imaging , ROC Curve , Reference Values , Retrospective Studies , Sensitivity and Specificity , Ultrasonography, Interventional
2.
Asian Journal of Andrology ; (6): 24-29, 2018.
Article in English | WPRIM | ID: wpr-1009523

ABSTRACT

Emerging evidence indicates that aldosterone and mineralocorticoid receptors (MRs) are associated with the pathogenesis of erectile dysfunction. However, the molecular mechanisms remain largely unknown. In this study, freshly isolated penile corpus cavernosum tissue from rats was treated with aldosterone, with or without MRs inhibitors. Nuclear factor (NF)-kappa B (NF-κB) activity was evaluated by real-time quantitative PCR, luciferase assay, and immunoblot. The results demonstrated that mRNA levels of the NF-κB target genes, including inhibitor of NF-κB alpha (IκB-α), NF-κB1, tumor necrosis factor-alpha (TNF-α), and interleukin 6 (IL-6), were higher after aldosterone treatment. Accordingly, phosphorylation of p65/RelA, IκB-α, and inhibitor of NF-κB kinase-β was markedly increased by aldosterone. Furthermore, knockdown of MRs prevented activation of the NF-κB canonical pathway by aldosterone. Consistent with this finding, ectopic overexpression of MRs enhanced the transcriptional activation of NF-κB by aldosterone. More importantly, the MRs antagonist, spironolactone blocked aldosterone-mediated activation of the canonical NF-κB pathway. In conclusion, aldosterone has an inflammatory effect in the corpus cavernosum penis, inducing NF-κB activation via an MRs-dependent pathway, which may be prevented by selective MRs antagonists. These data reveal the possible role of aldosterone in erectile dysfunction as well as its potential as a novel pharmacologic target for treatment.


Subject(s)
Animals , Male , Rats , Aldosterone/pharmacology , Cytokines/biosynthesis , Gene Knockdown Techniques , I-kappa B Kinase/antagonists & inhibitors , Interleukin-6/genetics , Mineralocorticoid Receptor Antagonists/pharmacology , NF-kappa B/genetics , Penis/metabolism , Protein Serine-Threonine Kinases/antagonists & inhibitors , RNA, Messenger/biosynthesis , Rats, Inbred WKY , Receptors, Mineralocorticoid/genetics , Signal Transduction/drug effects , Spironolactone/pharmacology , Transcriptional Activation , Tumor Necrosis Factor-alpha/biosynthesis , NF-kappaB-Inducing Kinase
SELECTION OF CITATIONS
SEARCH DETAIL