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1.
National Journal of Andrology ; (12): 122-127, 2016.
Article in Chinese | WPRIM | ID: wpr-304740

ABSTRACT

<p><b>OBJECTIVE</b>To determine the expression of Skp2 in different prostate cancer (PCa) cell lines and tissues, and explore its influence on the androgen receptor (AR) signaling pathway and development of castration-resistant prostate cancer (CRPC).</p><p><b>METHODS</b>The expression levels of Skp2 and AR in different PCa cell lines were detected by Western blot. After knockdown of Skp2 in the C4-2 and 22RV1 cells transfected with shRNA, the expressions of AR and P27 were determined and the activity of ARR3-Luc measured by dual-luciferase reporter gene assay following treatment with dihydrotestosterone (DHT). The expressions of AR and Skp2 in human naïve PCa or CRPC specimens were detected by immunohistochemical staining followed by analysis of their differences and correlation.</p><p><b>RESULTS</b>The Skp2 protein expression level was significantly higher in the C4-2 or 22RV1 cells than in the LNCaP cells. DHT treatment increased the expression of Skp2 in the C4-2 cells, but knock-down of Skp2 significantly up-regulated the expression of the well-known downstream protein P27 and down-regulated that of AR. Consistently, DHT treatment increased the activity of ARR3-Luc, while knockdown of Skp2 remarkably decreased it in the C4-2 and 22RV1 cells (P < 0.05). In addition, significantly higher expressions of Skp2 and AR were observed in the CRPC than in the naïve specimens (P < 0.05), with a positive correlation between the two proteins (r = 0.658 1, P < 0.05).</p><p><b>CONCLUSION</b>Skp2 can enhance the expression and transcription activity of the AR protein in CRPC cells or tissues and is promising to be a critical molecular therapeutic target.</p>


Subject(s)
Humans , Male , Androgens , Pharmacology , Cell Line, Tumor , Dihydrotestosterone , Pharmacology , Disease Progression , Gene Knockdown Techniques , Neoplasm Proteins , Genetics , Metabolism , Prostatic Neoplasms, Castration-Resistant , Metabolism , Receptors, Androgen , Genetics , Metabolism , S-Phase Kinase-Associated Proteins , Physiology , Transcriptional Activation , Up-Regulation
2.
China Journal of Chinese Materia Medica ; (24): 1096-1098, 2005.
Article in Chinese | WPRIM | ID: wpr-239741

ABSTRACT

<p><b>OBJECTIVE</b>To compare the actions of the three flavone ingredients in choerospondias axillaris on arrhythmias Induced by aconitine.</p><p><b>METHOD</b>Langendorff perfuse was applied in the experiment, the antiarrhythmic action was to study by using aconitine on the the isolated heart; The antiarrhythmic action of the three flavone ingredients in choerospondias axillaris was to study by using i.v. aconitine in rat to induce arrhythmias.</p><p><b>RESULT</b>Compared with the NS group, sample 1 and sample 2 both significantly prolonged the beginning time of VF of isolated heart and increased the dosage of aconitine, sample 3 reduced the beginning time of VF of isolated heart and decreased the dosage of aconitine, sample 1 and sample 2 both greatly prolonged the beginning time of VE, VT, VF, HA; sample 3 greatly reduced the beginning time of VT,VF. The actions of the three samples were in a concentration-dependent way.</p><p><b>CONCLUSION</b>Sample 1 and sample 2 both resisted the occurrence of arrhythmias induced by aconitine, sample 3 markedly promoted the occurrence of arrhythmias induced by aconitine.</p>


Subject(s)
Animals , Female , Male , Rats , Aconitine , Anacardiaceae , Chemistry , Anti-Arrhythmia Agents , Therapeutic Uses , Arrhythmias, Cardiac , Dose-Response Relationship, Drug , Flavones , Therapeutic Uses , In Vitro Techniques , Phytotherapy , Plants, Medicinal , Chemistry , Random Allocation , Rats, Wistar
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