首页> 外文期刊>Molecular biology reports >Novel ultrasound-targeted microbubble destruction mediated short hairpin RNA plasmid transfection targeting survivin inhibits gene expression and induces apoptosis of HeLa cells
【24h】

Novel ultrasound-targeted microbubble destruction mediated short hairpin RNA plasmid transfection targeting survivin inhibits gene expression and induces apoptosis of HeLa cells

机译:靶向survivin的新型超声靶向微泡破坏介导的短发夹RNA质粒转染抑制基因表达并诱导HeLa细胞凋亡

获取原文
获取原文并翻译 | 示例
           

摘要

Survivin is an attractive target for tumor growth inhibition and represents a significant approach to anticancer therapy. RNA interference is an important tool for specifically down-regulating the expression of cellular genes. However, the efficiency of short hairpin RNA (shRNA) on the expression of survivin gene and the influence on the cell apoptosis transfected by the non-viral gene transfer system of ultrasound-targeted microbubble destruction was not explored. In this work, recombinant expression plasmid of shRNA targeting survivin gene was constructed and added to cultured cervical cancer cells followed by ultrasound exposure and SonoVuep microbubble. Expression of survivin mRNA and protein were assessed by RT-PCR and western blot analysis. Apoptosis ratio was quantified by flow cytometry marked with annexin V and 7-AAD. After transfected for 48 h, the expression of survivin mRNA and protein were (16.67 pl 2.73)% and (21.33 pl 3.55)%, respectively. The apoptosis rate was (45.41 pl 1.47)%. The differences were significant as compared with other groups (P < 0.01). In conclusion, we suggested that survivin could be regarded as an ideal anticancer target of cervical cancer. Recombinant expression plasmid of shRNA targeting survivin gene mediated by ultrasound-targeted microbubble destruction technique could effectively inhibit the expression of target gene and induce cell apoptosis. This novel method for RNA interference represents a powerful, promising non-viral technology that can be used in the tumor gene therapy and research.
机译:Survivin是抑制肿瘤生长的诱人靶标,是抗癌治疗的重要方法。 RNA干扰是特异性下调细胞基因表达的重要工具。然而,未探讨短发夹RNA(shRNA)对survivin基因表达的效率以及超声靶向微泡破坏的非病毒基因转移系统对转染细胞凋亡的影响。在这项工作中,构建了靶向survivin基因的shRNA重组表达质粒,并将其添加到培养的宫颈癌细胞中,然后进行超声波照射和SonoVuep微泡。通过RT-PCR和蛋白质印迹分析评估survivin mRNA和蛋白的表达。通过用膜联蛋白V和7-AAD标记的流式细胞术定量凋亡率。转染48小时后,survivin mRNA和蛋白的表达分别为(16.67 pl 2.73)%和(21.33 pl 3.55)%。凋亡率为(45.41pl 1.47)%。与其他组相比,差异具有统计学意义(P <0.01)。总之,我们建议存活蛋白可以被视为宫颈癌的理想抗癌靶标。超声靶向微泡破坏技术介导的靶向survivin基因的shRNA重组表达质粒可有效抑制靶基因的表达并诱导细胞凋亡。这种用于RNA干扰的新方法代表了一种强大而有前途的非病毒技术,可用于肿瘤基因治疗和研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号