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Slug-siRNA干扰Slug基因表达对胰腺癌的抑制作用
引用本文:欧树安,张克君,严明总,王齐全.Slug-siRNA干扰Slug基因表达对胰腺癌的抑制作用[J].世界华人消化杂志,2009,17(17).
作者姓名:欧树安  张克君  严明总  王齐全
作者单位:1. 海南医学院附属医院普外科,海南省海口市,527000
2. 海南省人民医院检验科,海南省海口市,527102
3. 海口市人民医院消化内科,海南省海口市,527102
摘    要:目的: 研究携带Slug-siRNA的rAAV对裸鼠体内胰腺癌的作用.方法: 建立人胰腺癌裸鼠皮下移植瘤模型,2wk后随机将建模成功的裸鼠分为3组,每组6只. 构建携带Slug-siRNA的rAAV载体,采用瘤体内多点注射的方法,阴性对照组裸鼠按1×109 puf(50 μL)标准注射rAAV-EGFP,空白对照组裸鼠注射等量生理盐水,实验组裸鼠按1×109 puf(50 μL)标准注射rAAV2-EGFP-slugsiRNA,只注射1次. 观察裸鼠的一般情况,摄食,活动能力,每周用电子天平秤体质量,绘制裸鼠生长曲线. 治疗6 wk后二氧化碳吸入法处死裸鼠,切取肿瘤称质量;免疫组织化学SP法检测slug蛋白的表达,TUNEL检测皮下移植瘤细胞凋亡,透射电镜检测细胞超微结构.结果: 3组裸鼠分别接受不同的处理后,在开始的2 wk皮下移植瘤的生长无明显差别,2 wk以后,实验组裸鼠皮下移植瘤的体积增长明显滞后于阴性对照组和空白对照组,差异有统计学意义( P<0.05). 治疗6 wk后,实验组裸鼠皮下移植瘤的质量明显轻于阴性对照组和空白对照组差异有统计学意义(3.26±0.48 g vs7.56±1.25 g,7.50±1.23 g,均P<0.05). 实验组裸鼠皮下移植瘤的AI值明显高于阴性对照组和空白对照组,差异有统计学意义(0.27±0.06vs 0.024±0.01,0.025±0.01,均P<0.05);实验组的抑瘤率明显高于阴性对照组,差异有统计学差异(71.4% vs 0.04%,P<0.01). 透射电镜下,实验组肿瘤细胞可见细胞器结构模糊,核固缩,染色质边集等现象. 免疫组织化学检测示实验组Slug表达明显减少.结论: Slug基因被有效沉默,Slug基因沉默后促进细胞凋亡,抑制胰腺癌实体瘤增殖和生长.

关 键 词:胰腺癌  基因治疗  免疫组织化学

Inhibitory effect of Slug gene silencing with siRNA on pancreatic cancer
Shu-An Ou,Ke-Jun Zhang,Ming-Zong Yan,Qi-Quan Wang.Inhibitory effect of Slug gene silencing with siRNA on pancreatic cancer[J].World Chinese Journal of Digestology,2009,17(17).
Authors:Shu-An Ou  Ke-Jun Zhang  Ming-Zong Yan  Qi-Quan Wang
Abstract:AIM: To study the effect on pancreatic cancer in rats of rAAV carrying Slug-siRNA to interfere Slug gene expression. METHODS: A model of subcutaneous tumor was generated through injection of human pancreatic cancer cells BxPC-3 into the nude mice,two weeks later,the nude mice were divided into 3 groups randomly with 6 per group. A recombinant adeno-associated virus vector containing Slug-siRNA gene (rAAV-Slug-siRNA) was constructed. By continuous infusions over 14 d,in negative controls,1×109 puf (50 μL) rAAV-EGFP was injected,while in black controls,50 μL normal saline was given,in experimental groups,1×109 puf (50 μL) rAAV2-EGFPslug-siRNA was injected. The general condition,feeding,activities of the rats,and weight were observed. The growth curve of the rats was drawn. After 6 wk,the rats were killed with CO2,and tumor tissues were cut off and weighed. The expression of Slug protein was detected using the IHC SP method,the apoptosis was detected by TUNEL,and the ultrastructure was detected with TEM.RESULTS: In the beginning of 2 wk,not any apparent growth change was found in three groups. But 2 wk later,the tumor grew slowly in experimental groups than in negative controls and blank controls (P < 0.05). After treatment of 6 wk,the tumor weight in experimental groups was lower than in negative control group or than blank controls group (3.26 ± 0.48 g vs 7.56 ± 1.25 g,7.50 ± 1.23 g,all P < 0.05). The AI was significant higher in experimental group than in the negative control group or blank control group (0.27 ± 0.06vs 0.024 ± 0.01,0.025 ± 0.01,all P < 0.05). The inhibitory rate was 71.4% in the experimental group,and 0.04% in the negative group,showing a significant difference (P < 0.01). Under TEM,the organelle had fuzzy structure,and karyopyknosis,chromatin margination was found in tumor cells in experimental group. The expression of Slug was down-regulated in experimental groups.CONCLUSION: RNAi-mediated Slug gene with rAAV silencing could transfect to pancreatic cancer cells and silence Slug effectively and selectively,which results in the growth and proliferation inhibition in pancreatic cancer in vivo.
Keywords:Slug-siRNA  Slug-siRNA  Pancreatic cancer  Gene therapy  Immunohistochemistry
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