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Construction of Ang2-siRNA chitosan magnetic nanoparticles and the effect on Ang2 gene expression in human malignant melanoma cells

机译:Ang2-siRNA壳聚糖磁性纳米粒的构建及其对人恶性黑色素瘤细胞Ang2基因表达的影响

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The aim of the present study was to construct angiopoietin-2 (Ang2)-small interfering (si) RNA chitosan magnetic nanoparticles and to observe the interference effects of the nanoparticles on the expression of the Ang2 gene in human malignant melanoma cells. Ang2-siRNA chitosan magnetic nanoparticles were constructed and transfected into human malignant melanoma cells in vitro. Red fluorescent protein expression was observed, and the transfection efficiency was analyzed. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to assess the inhibition efficiency of Ang2 gene expression. Ang2-siRNA chitosan magnetic nanoparticles were successfully constructed, and at a mass ratio of plasmid to magnetic chitosan nanoparticles of 1: 100, the transfection efficiency into human malignant melanoma cells was the highest of the ratios assessed, reaching 61.17%. RT-qPCR analysis showed that the magnetic chitosan nanoparticles effectively inhibited Ang2 gene expression in cells, and the inhibition efficiency reached 59.56% (P<0.05). Ang2-siRNA chitosan magnetic nanoparticles were successfully constructed. The in vitro studies showed that the nanoparticles inhibited Ang2 gene expression in human malignant melanoma tumor cells, which laid the foundation and provided experimental evidence for additional future in vivo studies of intervention targeting malignant melanoma tumor growth in nude mice.
机译:本研究的目的是构建血管生成素2(Ang2)-小干扰(si)壳聚糖磁性纳米粒子,并观察纳米粒子对人恶性黑色素瘤细胞Ang2基因表达的干扰作用。 Ang2-siRNA壳聚糖磁性纳米粒子被构建并在体外转染到人类恶性黑色素瘤细胞中。观察到红色荧光蛋白表达,并分析了转染效率。使用逆转录定量聚合酶链反应(RT-qPCR)评估Ang2基因表达的抑制效率。成功构建了Ang2-siRNA壳聚糖磁性纳米颗粒,质粒与磁性壳聚糖纳米颗粒的质量比为1:100,转染至人恶性黑色素瘤细胞的效率最高,达到61.17%。 RT-qPCR分析表明,磁性壳聚糖纳米粒能有效抑制Ang2基因在细胞中的表达,抑制效率达到59.56%(P <0.05)。成功构建了Ang2-siRNA壳聚糖磁性纳米粒子。体外研究表明,纳米颗粒抑制了人类恶性黑色素瘤肿瘤细胞中的Ang2基因表达,这为裸鼠恶性黑色素瘤肿瘤生长的干预研究提供了基础并提供了实验证据。

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