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首页> 外文期刊>Japanese journal of radiology >Suppression of vascular endothelial growth factor via siRNA interference modulates the biological behavior of human nasopharyngeal carcinoma cells
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Suppression of vascular endothelial growth factor via siRNA interference modulates the biological behavior of human nasopharyngeal carcinoma cells

机译:通过siRNA干扰抑制血管内皮生长因子调节人鼻咽癌细胞的生物学行为

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Purpose. The aim was to study the effect of vascular endothelial growth factor (VEGF) down-regulation by small interfering (si)RNA-mediated interference (RNAi) on the biological features of nasopharyngeal carcinoma cell line CNE-2. Materials and methods. The combined plasmids pUsiVEGF and pU-siCONT were transfected into CNE-2 cells with lipofectamine. The transfected cells were placed in fresh medium containing G418. Expression of VEGF mRNA and protein were measured by reverse transcriptase-polymerase chain reaction and Western blot, respectively. The transwell chamber model was employed to test the ability of cell invasion in vitro. The distribution of cell cycle phases was determined by flow cytometry. Cell survival was assessed by clonogenic assays. Results. Both VEGF mRNA and protein expression were significantly decreased in the pU-siVEGF group compared with controls (P < 0.05). The cell cycle was arrested in the G1 phase (P < 0.05). A higher apoptotic ratio and lower invasion ability were seen in the pUsiVEGF group. The D0 (mean lethal dose) and SF2 values were significantly lower than those in the control group (P < 0.05). Conclusion. Delivery of siRNA targeting VEGF seems efficient in down-regulating VEGF expression and diminishing the growth, proliferation, and invasiveness of CNE-2 cells. It also enhanced the sensitivity of CNE-2 cells to radiation.
机译:目的。目的是研究小干扰(si)RNA介导的干扰(RNAi)引起的血管内皮生长因子(VEGF)下调对鼻咽癌细胞系CNE-2生物学特性的影响。材料和方法。用脂质转染胺将合并的质粒pUsiVEGF和pU-siCONT转染到CNE-2细胞中。将转染的细胞置于含有G418的新鲜培养基中。 VEGF mRNA和蛋白的表达分别通过逆转录-聚合酶链反应和蛋白质印迹法测量。用transwell室模型测试体外细胞侵袭的能力。细胞周期相的分布通过流式细胞术确定。细胞存活通过克隆形成测定来评估。结果。与对照组相比,pU-siVEGF组的VEGF mRNA和蛋白表达均显着降低(P <0.05)。细胞周期停滞在G1期(P <0.05)。 pUsiVEGF组细胞凋亡率较高,侵袭能力较低。 D 0 (平均致死剂量)和SF 2 值显着低于对照组(P <0.05)。结论。靶向VEGF的siRNA的递送似乎在下调VEGF表达和减少CNE-2细胞的生长,增殖和侵袭性方面有效。它还增强了CNE-2细胞对辐射的敏感性。

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