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1.
Experimental & Molecular Medicine ; : e429-2018.
Article in English | WPRIM | ID: wpr-739496

ABSTRACT

This study investigated the effects of microRNA-135a (miR-135a) targeting of glycogen synthase kinase 3β (GSK3β) on the epithelial–mesenchymal transition (EMT), migration and invasion of bladder cancer (BC) cells by mediating the Wnt/β-catenin signaling pathway. BC and adjacent normal tissues were collected from 165 BC patients. Western blotting and quantitative real-time PCR were used to detect the expression of GSK3β, β-catenin, cyclinD1, E-cadherin, vimentin and miR-135a in BC tissues and cells. Cells were assigned to blank, negative control (NC), miR-135a mimics, miR-135a inhibitors, small interfering RNA (siRNA)-GSK3β or miR-135a inhibitors+siRNA-GSK3β groups. miR-135a, β-catenin, cyclinD1 and vimentin expression increased, while GSK3β and E-cadherin expression decreased in BC tissues compared with adjacent normal tissues. Compared with the blank and NC groups, the expression of miR-135a, β-catenin, cyclinD1 and vimentin was higher, and cell proliferation, migration, invasion and tumor growth were increased in the miR-135a mimics and siRNA-GSK3β groups. These groups showed an opposite trend in GSK3β and E-cadherin expression and cell apoptosis. The miR-135a inhibitors group was inversely correlated with the blank and NC groups. It was concluded that miR-135a accelerates the EMT, invasion and migration of BC cells by activating the Wnt/β-catenin signaling pathway through the downregulation of GSK3β expression.


Subject(s)
Humans , Apoptosis , Blotting, Western , Cadherins , Cell Proliferation , Down-Regulation , Glycogen Synthase Kinases , Negotiating , Real-Time Polymerase Chain Reaction , RNA, Small Interfering , Urinary Bladder Neoplasms , Urinary Bladder , Vimentin
2.
Chinese Journal of Gastrointestinal Surgery ; (12): 842-845, 2010.
Article in Chinese | WPRIM | ID: wpr-266260

ABSTRACT

<p><b>OBJECTIVE</b>To explore the impact of abnormal myoelectricity at gastroduodenal anastomosis on gastric emptying in rats.</p><p><b>METHODS</b>Rats were randomly divided into experimental group (n=16) and control group (n=16). Pylorectomy and end-to-end gastroduodenal anastomosis were performed in the experimental group and electrodes were implanted in the serosal surface adjacent to the anastomosis. Slow waves were recorded by the implanted electrode in vivo. Gastric emptying was examined by scintigraphy.</p><p><b>RESULTS</b>At the first week after surgery, antral slow-wave frequency was significantly lower in the experimental group (0.8±1.4 vs. 3.3±1.2, P<0.01), as was the duodenal slow-wave frequency (2.1±0.6 vs. 11.1±0.7, P<0.01). There was no consecutive slow-waves transduction across the pylorus or the anastomosis. Within 12-16 weeks after operation, antral slow-wave frequency in the experimental group and the control group were (8.7±0.6) cpm and (4.0±0.4) cpm, respectively (P<0.01), and duodenal slow-wave frequency were (11.1±0.8) cpm and (10.8±0.7) cpm, respectively (P>0.05). Retrograde and antegrade myoelectricity transduction through the anastomosis were detected. The mean semi-emptying time in the proximal stomach was 14.7 min in the experimental group and 13.6 min in the control group (P>0.05). Radionuclide retention rate was 25.4% in the experimental group and 39.4% in the control group (P>0.05). The mean semi-emptying time in the distal stomach was 25.3 min in the experimental group and 10.5 min in the control group (P<0.01). Radionuclide retention rate was 46.4% in the experimental group and 18.7% in the control group (P<0.01).</p><p><b>CONCLUSION</b>The abnormal myoelectricity in the region of gastroduodenal stoma may delay liquid gastric emptying in pylorectomy rats.</p>


Subject(s)
Animals , Male , Rats , Duodenum , Physiology , General Surgery , Gastric Emptying , Physiology , Gastroenterostomy , Myoelectric Complex, Migrating , Physiology , Rats, Sprague-Dawley , Surgical Stomas , Physiology
3.
Journal of Zhejiang University. Medical sciences ; (6): 100-102, 2009.
Article in Chinese | WPRIM | ID: wpr-310384

ABSTRACT

<p><b>OBJECTIVE</b>To evaluate the feasibility and safety of transperitoneal laparoscopic nephrectomy in live-donors.</p><p><b>METHODS</b>Two cases of live-donor underwent laparoscopic nephrectomy in May and August 2008 respectively and both were followed up.</p><p><b>RESULT</b>In two cases the operation time was 130, 10 min; blood loss was 50 ml; warm ischemic time was 30 s and 2 min; the length of artery was 4.0 cm and 3.5 cm; the length of vein was 3.0 cm. The grafted kidneys started to produce urine at 30 s and 10 s after blood supply. Renal function of donor returned to normal after two days. The donors were discharged at 7th day after the operation. Renal function of recipient was normal after 3 days.</p><p><b>CONCLUSION</b>Transperitoneal laparoscopic nephrectomy in live-donor is a safe and effective procedure, which provides kidney with satisfactory blood vessels and ureter for graft.</p>


Subject(s)
Female , Humans , Male , Middle Aged , Kidney Transplantation , Laparoscopy , Living Donors , Nephrectomy , Methods , Peritoneum , General Surgery , Tissue and Organ Harvesting
4.
Chinese Journal of Surgery ; (12): 225-227, 2003.
Article in Chinese | WPRIM | ID: wpr-300042

ABSTRACT

<p><b>OBJECTIVE</b>To develop a method performed on an oligonucleotide array for HLA-DR53 group genotyping.</p><p><b>METHODS</b>According to the specific allelic frequency and sequence of HLA-DRB loci in Chinese Han population, HLA-DR53 group typing probes which were immobilized on a glass supports were synthesized. A pair of group-special primers labeled by the Cy5-dCTP were designed, and the primers were used in the PCR, thus the PCR products were labeled with Cy5. The labeled PCR products were hybridized with array. The signals were scanned by scanner and analyzed by image software. The typing results were confirmed by standard DNA and PCR-SSO. One hundred and eleven samples were typed by this array.</p><p><b>RESULTS</b>There were 72 HLA-DR53 group loci typed by oligonucleotide array. Among them, 34 loci were DR9, 25 were DR4, and 13 were DR7. No false positive or false negative typing results were observed. The specificity and reproducibility were 100% and the overall time of genotyping was 5 hours.</p><p><b>CONCLUSION</b>The oligonucleotide array technique is a precise, rapid molecular method for HLA-DR53 genotyping, suited for clinical practice.</p>


Subject(s)
Humans , Genotype , HLA-DR Antigens , Genetics , HLA-DRB4 Chains , Oligonucleotide Array Sequence Analysis , Reproducibility of Results , Sensitivity and Specificity
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