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Slug-siRNA干扰Slug基因表达对胰腺癌的抑制作用 被引量:4

Inhibitory effect of Slug gene silencing with siRNA on pancreatic cancer
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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1×109puf(50μL)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1×109puf(50μL)标准注射rAAV2-EGFP-slug-siRNA,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6wk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2wk皮下移植瘤的生长无明显差别,2wk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6wk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±0.48gvs7.56±1.25g,7.50±1.23g,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±0.06vs0.024±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%vs0.04%,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. 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, 1×10^9puf (50 μL) rAAV-EGFP was injected, while in black controis, 50 μL normal saline was given, in experimental groups, 1×10^9 puf (50 μL) rAAV2-EGFP- slug-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 ± 0.06 vs 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, show- ing 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 experimental groups. was down-regulated in CONCLUSION: RNAi-mediated Slug gene with rAAV silencing could transfect to pancreatic cancer cells and silence Slug effectively and se- lectively, which results in the growth and proliferation inhibition in pancreatic cancer in vivo.
出处 《世界华人消化杂志》 CAS 北大核心 2009年第17期1713-1719,共7页 World Chinese Journal of Digestology
关键词 Slug—siRNA 胰腺癌 基因治疗 免疫组织化学 Slug-siRNA Pancreatic cancer Gene therapy Immunohistochemistry
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  • 1张克君,李德春.重组腺病毒mIκBα基因的构建及体外抑制血管生成的作用[J].苏州大学学报(医学版),2006,26(4):543-546. 被引量:3
  • 2张克君,李德春.核因子κB在胰腺癌中的表达及与VEGF和p53表达的相关性[J].肿瘤防治研究,2006,33(11):805-807. 被引量:4
  • 3张克君,李德春,朱新国,朱东明,赵志泓.外源野生型p53正向细胞凋亡调控因子基因对人胰腺癌PC-3细胞生长的作用[J].中华消化杂志,2006,26(11):778-779. 被引量:11
  • 4Lohr JM. Medical treatment of pancreatic cancer. Expert Rev Anticancer Ther, 2007, 7(4): 533-544.
  • 5Edelstein ML, Abedi MR, Wixon J. Gene therapy clinical trials worldwide to 2007-an update. Gene Med, 2007, 9 (10) : 833- 842.
  • 6Yu J, Zhang L, Hwang PM, et al. PUMA induces the rapid apoptosis of colorectal cancer cells. Mol Cell, 2001,7(3) : 673-682.
  • 7Nakano K, Vousden KH. PUMA, a novel proapoptotic gene, is induced by p53. Mol Cell, 2001,7(3) : 683-694.
  • 8Chen Y, Qian H, Wang H, et al. Ad-PUMA sensitizes drug-resistant choriocarcinoma cells to chemotherapeutic agents. Gynecol Oneol, 2007, 107(3) : 505-512.
  • 9Ito H, Kanzawa T, Miyoshi T, et al. Therapeutic efficacy of PUMA for malignant glioma ceils regardless of p53 status. Hum Gene Ther, 2005, 16(6) : 685-698.
  • 10Yu J, Yue W, Wu B, et al. PUMA sensitizes lung cancer cells to chemotherapeutic agents and irradiation. Clin Cancer Res, 2006, 12(9) : 2928-2936.

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  • 1倪志,刘南植,李林芳,张庆,李秀梅,洪玮.5-Aza-CdR对人结肠癌Lovo细胞增殖凋亡及抑癌基因RUNX3表达的影响[J].世界华人消化杂志,2006,14(2):184-188. 被引量:6
  • 2靳西凤,冉志华.RNA干扰技术与结肠癌[J].世界华人消化杂志,2006,14(20):2003-2008. 被引量:4
  • 3Savagner P,Yamada KM,Thiery JP.The zinc-finger protein slug causes desmosome dissociation,an initial and necessary step for growth factor-induced epithelial-mesenchymal transition.J Cell Biol,1997,137:1403-1419.
  • 4Hajra KM,Chen DY,Fearon ER.The SLUG zinc-finger protein represses E-cadherin in breast cancer.Cancer Res,2002,62:1613-1618.
  • 5Sugimachi K,Tanaka S,Kameyama T.Transcriptional repressor snail and progression of human hepatocellular carcinoma.Clin Cancer Res,2003,9:2657-2664.
  • 6Uchikado Y,Natsugoe S,Okumura H.Slug Expression in the E-cadherin preserved tumors is related to prognosis in patients with esophageal squamous cell carcinoma.Clin Cancer Res,2005,11:1174-1180.
  • 7Shih JY,Tsai MF,Chang TH,et al.Transcription repressor slug promotes carcinoma invasion and predicts outcome of patients with lung adenocarcinoma.Clin Cancer Res,2005,11:8070-8088.
  • 8Shioiri M,Shida T,Koda K,et al.Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients.Br J Cancer,2006,94:1816-1822.
  • 9Thiery JP.Epithelialmesenchymal transitions in tumour progression.Nat Rev Cancer,2002,2:442-454.
  • 10Sun D,Baur S,Hay ED.Epithelial mesenchymal transformation is the mechanism for fusion of the craniofacial primordia involved in morphogenesis of the chicken lip.Dev Biol,2000,228:337-349.

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