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find Author "LI Chengjie" 3 results
  • Clinical Application of Filter Planting Associated with Thrombolysis Therapy in the Management of Deep Venous Thrombosis of Lower Limbs

    【摘要】 目的 〖JP2〗评价腔静脉滤器植入联合足背静脉溶栓在下肢深静脉血栓(DVT)治疗中的疗效。 方法 2006年12月-2009年10月,对26 例下肢深静脉血栓患者行下腔静脉滤器植入术,并结合足背静脉溶栓治疗。 结果 26例患者均未出现大出血和致死性肺动脉栓塞等严重并发症,彩色多普勒超声显示17例患者下肢DVT 完全溶解,11例部分溶解。 结论 介入性综合治疗下肢DVT 是一种安全可行、疗效好的方法。【Abstract】 Objective To evaluate the therapeutic effect of filter planting combining thrombolysis therapy through the dorsum pedis vein on patients with deep veins thrombosis of lower limb. Methods The clinical data of 26 patients from December 2006 to October 2009 were retrospectively analyzed. All the patients underwent filter planting combining thrombolysis therapy through the dorsum pedis vein. Results There was no serious complication such as hemorrhea or fatal pulmonary embolism. The phlebothrombosis was fully dissolved in 11 patients and partial dissolved in 17 patients. Conclusion Interventional combined therapy is safe and effective for deep venous thrombosis of lower limb.

    Release date:2016-09-08 09:51 Export PDF Favorites Scan
  • The Diagnostic Value of Abdomen and Chest Xray for Aute Pancreatitis

    目的:探讨急性胰腺炎的胸腹部X线平片显示特征及诊断。方法:回顾分析19例急性重症胰腺炎的胸腹部X线平片资料,总结其影像特征。结果:急性胰腺炎胸腹部X线平片显示反射性肠郁积15例,十二指肠曲部见弧形压迹1例, 剑突下胰腺区高密度影1例,麻痹性肠梗阻伴胸腔积液2例。结论:胸腹部X线平片经济,快捷,在急性胰腺炎早期诊断中有一定价值。

    Release date:2016-09-08 10:01 Export PDF Favorites Scan
  • Influence of Liposomal Transfection of Survivin Antisense Oligodeoxynucleotide on Human Pancreatic Cancer Cells

    Objective To investigate the inhibitory effect of survivin antisense oligonucleotides (ASODN) on proliferation of pancreatic cancer cells PANC-1. Methods The ASODN and sense oligodeoxynucleotides (SODN) were complementary to survivin sequences. FAM-marked ASODN was transfected into PANC-1 cells mediated by positive ion liposome as ASODN group. Blank control group (normal cells), negative control group (normal medium), and SODN group were established for comparison. The transfection efficiency was detected by flow cytometry (FCM) after transfection; MTT assay was used to detect cytotoxicity; Cell morphological changes were examined by transmission electron microscopy; The cell cycle and apoptotic rate were analyzed by FCM; Immunohistochemical staining techniques were used, and the expressions of survivin were observed under light microscopy, examined and analysed by computer image. Results ①The transfection efficiency was 31.9%, 37.4%, 41.4%, 52.6%,  24.2%, 11.4%, 16.1%, and 15.5% when the transfecting concentration of ASODN was 50, 100, 150, 200, 250, 400, 600, and 800 nmol/L, respectively; The transfection efficiency was 12.0%, 50.8%, and 11.2% when the inoculated cells was 2×104/well, 2×105/well, and 2×106/well, respectively; The transfection efficiency was  58.8%,  34.0%, and 23.6% when 2 μl, 3 μl, and 4 μl liposome was used during transfection, respectively. ②Cell gap was oversize, morphous was round, adherent cells were less after transfection under fluorescence microscope. ③The inhibition rate in the ASODN group was higher than that in each control group (Plt;0.05) on 24, 36, 48 h after treating by survivin ASODN, which increased as time prolonged (Plt;0.05). ④The apoptosis showed a ladder-shaped line in the ASODN group. ⑤Apoptotic morphology was demonstrated in the ASODN group, such as apoptotic cells with nuclear chromatin highly concentrated, crescent nuclear staining aggregated by the side nuclear membrane, nucleolus disappeared by AO and EB stains. ⑥The apoptotic rate 〔(38.1±3.4)%〕 in the ASODN group was higher than that in the SODN group 〔(4.16±1.7)%〕, Plt;0.05. ⑦G2/M cell cycle arrested in the ASODN group. ⑧After transfection, the expression of survivin protein in the ASODN group was significantly lower than that of each control group (Plt;0.05). Conclusions The optimal transfection conditions are as following: the cell count of 2×105/well, concentration of ASODN 200 nmol/L, and cationic liposome oligofectamine 2 μl, respectively. Survivin ASODN can inhibit the proliferation of pancreatic cancer cells and induce their apoptosis.

    Release date:2016-09-08 10:50 Export PDF Favorites Scan
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