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Cationic Nanoparticles Effectively Delivered VEGF SiRNA in A549 Cells

机译:阳离子纳米颗粒有效地在A549细胞中传递VEGF SiRNA

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Vascular endothelial growth factor (VEGF) plays a crucial role in the production of new blood vessels (angiogenesis) needed for cell growth and proliferation, and tumor expansion. Therefore, inhibition of angiogenesis via targeting the VEGF signalling pathway offers a target for cancer therapy. Small interfering RNAs (SiRNAs) are specific inhibitors of mRNA, block the translation step, and inhibit the expression of protein in the tumor cells. The challenge with SiRNA as therapeutic agents is its inherent instability in biological fluids. We propose to overcome this by encapsulating the SiRNA in nanoparticles, which has the potential to provide improved effectiveness and safety for cancer treatment. In this study, we validated this approach of inhibition of VEGF levels using SiRNA in lung cancer cells. Cationic nanoparticles of SiRNA were prepared and characterized. No significant injury to the cells was observed after cells were treated with SiRNA nanoparticles. Cationic Liposomes of VEGF SiRNA showed the most effecacy in inhibiting expression of VEGF in A549 lung cancer cells.
机译:血管内皮生长因子(VEGF)在细胞生长和增殖以及肿瘤扩张所需的新血管的产生(血管生成)中起着至关重要的作用。因此,通过靶向VEGF信号传导途径抑制血管生成提供了癌症治疗的靶标。小干扰RNA(SiRNA)是mRNA的特异性抑制剂,可阻止翻译步骤并抑制肿瘤细胞中蛋白质的表达。 SiRNA作为治疗剂的挑战是其在生物体液中固有的不稳定性。我们建议通过将SiRNA封装在纳米颗粒中来克服这一问题,这有可能为癌症治疗提供提高的有效性和安全性。在这项研究中,我们验证了使用SiRNA在肺癌细胞中抑制VEGF水平的方法。制备并表征了SiRNA的阳离子纳米粒子。用SiRNA纳米颗粒处理细胞后,未观察到对细胞的明显损伤。 VEGF SiRNA的阳离子脂质体在抑制A549肺癌细胞中VEGF表达方面显示出最有效的功效。

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