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生存素siRNA表达质粒对结肠癌细胞侵袭和增殖能力的抑制作用[J]. 肿瘤防治研究, 2008, 35(07): 471-475. DOI: 10.3971/j.issn.1000-8578.1867
引用本文: 生存素siRNA表达质粒对结肠癌细胞侵袭和增殖能力的抑制作用[J]. 肿瘤防治研究, 2008, 35(07): 471-475. DOI: 10.3971/j.issn.1000-8578.1867
siRNA Aiming at survivin Inhibit Invasive Ability and Proliferation of Colorectal Cancer Cell Line[J]. Cancer Research on Prevention and Treatment, 2008, 35(07): 471-475. DOI: 10.3971/j.issn.1000-8578.1867
Citation: siRNA Aiming at survivin Inhibit Invasive Ability and Proliferation of Colorectal Cancer Cell Line[J]. Cancer Research on Prevention and Treatment, 2008, 35(07): 471-475. DOI: 10.3971/j.issn.1000-8578.1867

生存素siRNA表达质粒对结肠癌细胞侵袭和增殖能力的抑制作用

siRNA Aiming at survivin Inhibit Invasive Ability and Proliferation of Colorectal Cancer Cell Line

  • 摘要: 目的 构建针对生存素的小分子RNA干扰表达质粒,研究siRNA表达质粒沉默生存素基因后对大肠癌细胞株SW480侵袭性和增殖性的影响。方法 用pRNAT U6.1/Neo载体构建生存素 siRNA表达质粒(pRNAT/sur-siRNA),该质粒转染SW480细胞株48小时后,用Westeron blot和半定量 RT-PCR分析生存素蛋白和mRNA表达的变化。G418 400μg/L筛选阳性克隆细胞株(sur-siRNA/SW480),MTT法检测SW480细胞体外增殖的变化;细胞侵袭性实验研究SW480细胞的侵袭性变化。结果 成功地构建了pRNAT/sur-siRNA表达质粒,并且该质粒明显下调SW480细胞生存素蛋白和mRNA的表达水平,分别下调85%,80%。G418 400μg/L筛选出转染pRNAT/sur-siRNA的SW480细胞株(sur-siRNA/SW480);sur-siRNA/SW480细胞增殖受到显著抑制,抑制率为37.4% (P<0.01);细胞侵袭实验示sur-siRNA/SW480细胞的穿透数为(153±66)个,而对照组pRNAT/SW480、SW480细胞的穿透数为(505±65),(578±98)个细胞,sur-siRNA/SW480细胞的穿透数与对照组相比显著减少(P<0.01)。结论 针对生存素siRNA可以显著降低生存素的表达,抑制肿瘤细胞的增殖和侵袭,该生存素siRNA序列可能成为治疗结肠癌的一种有效手段。

     

    Abstract: Objective To construct expression vectors of small RNA interference aimed at survivin gene and to explore effect of survivin siRNA gene on proliferation and invasive ability of SW480 cell line. Methods A survivin siRNA plasmid (pRNAT/sur-siRNA)was constructed using pRNAT U6.1/Neo vector. After pRNAT/sur-siRNA vectors were transduced into SW480 cell line 48 hours, the expression level of survivin mRNA and protein were measured by semi-quantitative reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis, the effect of pRNAT/sur-siRNA vectors on SW480 cell line proliferation and invasive ability were evaluated by MTT assay and cell invasion experiment, respectively. Results survivin siRNA expression plasmid (pRNAT/sur-siRNA)was constructed successfully and pRNAT/sur-siRNA down-regulated expression level of survivin gene protein and mRNA dramatically in SW480 cell,85%,80% respectively. SW480 cell containing pRNAT/sur-siRNA vectors (sur-siRNA/SW480) was selected by G418 400μg/L. MTT assay showed proliferation of sur-siRNA/SW480 cell was inhibited obviously (inhibition ratio was 37.4%), lower than proliferation of control group cell (P<0.01). Cell invasion experiment showed that cell numbers of sur-siRNA/SW480, pRNAT/SW480 and SW480 cell, that penetrated membrance, were 153±66, 505±65 and 578±98, penetration numbers of sur-siRNA/SW480 cell was reduced obviously, compare to control groups cell (P<0.01). Conclusion The siRNA aimed at survivin gene could reduce the expression level of survivin gene protein and mRNA, and inhibit proliferation and invasive ability of SW480 cell line. The sequence of RNA interference against survivin may be a validity method to treat colorectal cancer.

     

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