Department of Medical Ultrasound, The Third Affiliated Hospital of Guangzhou Medical College, Guangzhou 510150, China.
Mol Biol Rep. 2009 Nov;36(8):2059-67. doi: 10.1007/s11033-008-9417-y. Epub 2008 Nov 9.
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 SonoVue((R)) 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 +/- 2.73)% and (21.33 +/- 3.55)%, respectively. The apoptosis rate was (45.41 +/- 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.
Survivin 是肿瘤生长抑制的一个有吸引力的靶标,代表了一种重要的抗癌治疗方法。RNA 干扰是特异性下调细胞基因表达的重要工具。然而,短发夹 RNA(shRNA)对 survivin 基因表达的抑制效率以及超声靶向微泡破坏的非病毒基因转染系统对细胞凋亡的影响尚未得到探索。在这项工作中,构建了靶向 survivin 基因的 shRNA 重组表达质粒,并在培养的宫颈癌细胞中加入超声暴露和 SonoVue(R)微泡。通过 RT-PCR 和 Western blot 分析评估 survivin mRNA 和蛋白的表达。通过流式细胞术用 annexin V 和 7-AAD 标记定量凋亡率。转染 48 小时后,survivin mRNA 和蛋白的表达分别为(16.67 +/- 2.73)%和(21.33 +/- 3.55)%。凋亡率为(45.41 +/- 1.47)%。与其他组相比,差异有统计学意义(P < 0.01)。总之,我们认为 survivin 可以作为宫颈癌的理想抗癌靶点。超声靶向微泡破坏技术介导的靶向 survivin 基因的重组表达质粒可以有效抑制靶基因的表达并诱导细胞凋亡。这种新的 RNA 干扰方法代表了一种强大的、有前途的非病毒技术,可用于肿瘤基因治疗和研究。