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1.
National Journal of Andrology ; (12): 790-793, 2011.
Article in Chinese | WPRIM | ID: wpr-305789

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of quercetin on the apoptosis of human PC-3 cells.</p><p><b>METHODS</b>Human PC-3 cells were cultured in vitro and then treated with quercetin at the concentrations of 50, 100, 150, 200 and 250 micromol/L. The inhibition rate of quercetin on the PC-3 cells was detected by MTT, the apoptosis of the cells determined by flow cytometry, and the changes of the cellular ultramicrostructure observed by transmission electron microscopy.</p><p><b>RESULTS</b>Quercetin markedly inhibited the proliferation of PC-3 cells in vitro in a time- and dose-dependent manner. Its inhibition rates were (3.01 +/- 1.32)%, (4.84 +/- 1.73)%, (20.35 +/- 1.30)%, (16.78 +/- 1.89)% and (27.25 +/- 4.01)% at 24 hours, and (10.18 +/- 1.16)%, (6.22 +/- 0.04)%, (24.29 +/- 4.19)%, (22.4 +/- 4.26)% and (41.42 +/- 5.43)% at 48 hours in the 50, 100, 150, 200 and 250 micromol/L groups, respectively, with statistical significance at the concentration of > 150 micromol/L (P < 0.05). Flow cytometry showed that the apoptosis of PC-3 cells was increased with the elevated concentration and prolonged time of Quercetin treatment, (19.10 +/- 0.28)% and (26.55 +/- 0.78)% at 24 hours, and (27.65 +/- 1.06)% and (38.30 +/- 5.96)% at 48 hours in the 150 and 200 micromol/L groups, respectively (P < 0.05). Typical changes in the morphology of the cells were observed under the transmission electron microscope.</p><p><b>CONCLUSION</b>Quercetin can inhibit the proliferation and induce the apoptosis of human PC-3 cells, but its action mechanism remains to be further investigated.</p>


Subject(s)
Humans , Male , Apoptosis , Cell Line, Tumor , Cell Proliferation , Flow Cytometry , Prostatic Neoplasms , Pathology , Quercetin , Pharmacology
2.
National Journal of Andrology ; (12): 907-910, 2008.
Article in Chinese | WPRIM | ID: wpr-309750

ABSTRACT

<p><b>OBJECTIVE</b>To compare the safety and efficacy of the two surgical alternatives, transurethral bipolar vaporization resection of the prostate (TUBVP) and holmium laser enucleation of the prostate (HOLEP), in the treatment of large benign prostatic hyperplasia (BPH).</p><p><b>METHODS</b>Retrospective analyses were made of 56 cases of large BPH ( >80 ml), 34 treated by TUBVP with the Bipolar Vaporization System (ACMI Medical Ltd, U.K.) at 160 W in cutting and 80 W in coagulation mode, and 22 by HOLEP with the Holmium Laser System (LUMNIS Ltd, US) at 100W. The safety and efficacy of the two approaches were assessed based on the operative and follow-up data.</p><p><b>RESULTS</b>Blood loss was significantly less in the HOLEP than in the TUBVP group ( P < 0.01), but the time of postoperative bladder irrigation and catheter indwelling was obviously shorter in the latter. IPSS, Qmax and Residual unine were markedly improved at 1 and 3 months after the surgery, with no statistically significant differences between the two groups.</p><p><b>CONCLUSION</b>Both TUBVP and HOLEP are safe and effective surgical options for the treatment of large BPH. Particularly the former, easier to be popularly applied, is promising to be a new "gold standard" in the surgical treatment of BPH.</p>


Subject(s)
Aged , Aged, 80 and over , Humans , Male , Lasers, Solid-State , Therapeutic Uses , Prostate , Pathology , Prostatic Hyperplasia , Pathology , General Surgery , Retrospective Studies , Transurethral Resection of Prostate , Methods
3.
National Journal of Andrology ; (12): 62-66, 2008.
Article in Chinese | WPRIM | ID: wpr-319290

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate two-dimensional gel electrophoresis (2DGE) and mass spectrometry in the studies of the serum proteins expressed in patients with BPH and those with high-grade prostatic intraepithelial neoplasm (HGPIN).</p><p><b>METHODS</b>We extracted serum proteins from BPH and HGPIN patients by 2DGE and cut the differentially expressed interesting protein spots from the gel. Then we digested the proteins, obtained the peptide mass fingerprint by mass spectrometry and identified the proteins through database retrieval.</p><p><b>RESULTS</b>We successfully achieved the 2DGE maps of the serum proteins from the BPH and HGPIN patients, obtained 1 421-1 532 protein spots from the 2D map of HGPIN and 1 466-1 778 from that of BPH. Based on peptide mass fingerprinting, 9 of the protein spots were identified. Serum amyloid A was found to be expressed in the HGPIN group, but weakly or not at all in the BPH.</p><p><b>CONCLUSION</b>Proteomics can be applied to the study of the serum proteins in BPH and HGPIN patients. It can afford experimental evidence for the early diagnosis and development HGPIN, promote the search of functional and specific proteins of prostate diseases and shed new light on the network mechanisms of the problems.</p>


Subject(s)
Humans , Male , Blood Proteins , Electrophoresis, Gel, Two-Dimensional , Mass Spectrometry , Prostatic Hyperplasia , Blood , Prostatic Intraepithelial Neoplasia , Blood , Prostatic Neoplasms , Blood , Proteome , Proteomics , Methods
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