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shRNA 介导Ku80 基因沉默对食管癌细胞及 裸鼠移植瘤生长的抑制作用[J]. 肿瘤防治研究, 2008, 35(12): 862-865. DOI: 10.3971/j.issn.1000-8578.1931
引用本文: shRNA 介导Ku80 基因沉默对食管癌细胞及 裸鼠移植瘤生长的抑制作用[J]. 肿瘤防治研究, 2008, 35(12): 862-865. DOI: 10.3971/j.issn.1000-8578.1931
Inhibitory Effect of Silencing Ku80 by shRNA on Esophageal Carcinoma Cells and Its Transplanted Models in Nude Mice[J]. Cancer Research on Prevention and Treatment, 2008, 35(12): 862-865. DOI: 10.3971/j.issn.1000-8578.1931
Citation: Inhibitory Effect of Silencing Ku80 by shRNA on Esophageal Carcinoma Cells and Its Transplanted Models in Nude Mice[J]. Cancer Research on Prevention and Treatment, 2008, 35(12): 862-865. DOI: 10.3971/j.issn.1000-8578.1931

shRNA 介导Ku80 基因沉默对食管癌细胞及 裸鼠移植瘤生长的抑制作用

Inhibitory Effect of Silencing Ku80 by shRNA on Esophageal Carcinoma Cells and Its Transplanted Models in Nude Mice

  • 摘要: 目的 利用shRNA 抑制Ku80 蛋白表达来研究Ku80 对食管癌细胞和裸鼠移植瘤生长的影响。方法 采用RNA 干扰技术,构建shRNA2Ku80 载体。用Western blot 和RT2PCR 方法证实RNA 干扰的有效性和可行性。用MTT 法、克隆形成实验和体内抑瘤实验来研究shRNA 抑制Ku80 表达对食管癌细胞和裸鼠移植瘤生长的影响。用流式分析法来研究shRNA 抑制Ku80 表达对细胞周期和凋亡的影响。结果 成功构建了shRNA2Ku80 载体。shRNA 抑制Ku80 表达在体内外抑制食管癌细胞的生长。shRNA 抑制Ku80 表达使细胞周期阻滞于G2 / M 期,促进射线引起的凋亡。结论 Ku80 在食管癌的发生、发展中起作用,shRNA 抑制Ku80 表达有望成为肿瘤基因治疗的靶点。

     

    Abstract: Objective  To investigate effect of Ku80 on esophageal carcinoma cells and it s t ransplanted models in nude mice, inhibition of Ku80 expression by shRNA vector was used. Methods  shRNA2Ku80 vector was const ructed, using RNA interference technology. The effectiveness and feasibility of RNA in2 terference were confirmed by Western blot and RT2PCR methods. Effect s of silencing Ku80 by shRNA on esophageal carcinoma cells and it s t ransplanted models in nude mice were investigated by MTT assay, Colony formation assay and inhibition of tumor assay in vi vo. Effect s of silencing Ku80 by shRNA on cell cycle and apoptosis were observed by Flow cytomet ry analysis. Results  ShRNA2Ku80 vector was con2 st ructed successfully. Silencing Ku80 by shRNA inhibited esophageal cells growth in vi t ro and i n vi vo. Silencing Ku80 by shRNA made cell cycle arrest in G2 / M phase and enhanced apoptosis induced by radia2 tion. Conclusion  Ku80 plays a role in occurrence and development of esophageal cancer, inhibition of Ku80 expression by shRNA may become a target of gene therapy of tumor.

     

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