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首页> 外文期刊>Colloids and Surfaces, B. Biointerfaces >Silencing of the metastasis-linked gene, AEG-1, using siRNA-loaded cholamine surface-modified gelatin nanoparticles in the breast carcinoma cell line MCF-7
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Silencing of the metastasis-linked gene, AEG-1, using siRNA-loaded cholamine surface-modified gelatin nanoparticles in the breast carcinoma cell line MCF-7

机译:在乳腺癌细胞系MCF-7中使用载有siRNA的胆胺表面修饰的明胶纳米颗粒沉默转移相关基因AEG-1

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Cholamine surface-modified gelatin nanoparticles prepared by the double desolvation method using acetone as a dehydrating agent were selected and potentially evaluated as non viral vectors of siRNA targeting a metastatic gene AEG-1 in MCF-7 breast carcinoma cells. The ability of modified gelatin nanoparticle to complex and deliver siRNA for gene silencing was investigated. Hence, Particle size, surface charge (zeta potential) and morphology of siRNA/Gelatin nanoparticles (siGNPs) were characterized via dynamic light scattering (DLS), scanning electron microscopy (SEM) and transmission electron microscope (TEM). Moreover, the nanoparticles cytotoxicity, loading efficiency and interaction with MCF-7 human breast carcinoma cells were evaluated. Cationized GNPs of mean size range of 174 nm and PDI of 0.101 were produced. The loading efficiency of siGNPs at a Nitrogen/Phosphate (N/P) ratio (w/w) of 200:1 was approximately 96%. Cellular uptake was evaluated after FITC conjugation where the particles produced high transfection efficiency. Finally, ELISA analysis of AEG-1/MTDH expression demonstrated the gene silencing effect of siGNPs, as more than 75% MTDH protein were inhibited. Our data indicate that cholamine modified GNPs pose a promising non-viral siRNA carrier for altering gene expression in MCF-7 breast cancer cells with many advantages such as relatively high gene transfection efficiency and efficient silencing ability. (C) 2016 Elsevier B.V. All rights reserved.
机译:选择通过使用丙酮作为脱水剂的双重去溶剂化方法制备的经氯胺表面改性的明胶纳米颗粒,并潜在地评估其作为靶向MCF-7乳腺癌细胞中转移基因AEG-1的siRNA的非病毒载体。研究了修饰的明胶纳米颗粒复合和递送用于基因沉默的siRNA的能力。因此,通过动态光散射(DLS),扫描电子显微镜(SEM)和透射电子显微镜(TEM)表征了siRNA /明胶纳米颗粒(siGNPs)的粒径,表面电荷(ζ电位)和形态。此外,评估了纳米颗粒的细胞毒性,负载效率以及与MCF-7人乳腺癌细胞的相互作用。产生平均大小范围为174 nm的阳离子化GNP,PDI为0.101。氮气/磷酸盐(N / P)比(w / w)为200:1时siGNP的加载效率约为96%。 FITC结合后评估细胞摄取,其中颗粒产生高转染效率。最后,对AEG-1 / MTDH表达的ELISA分析证明了siGNP的基因沉默作用,因为抑制了超过75%的MTDH蛋白。我们的数据表明,胆胺修饰的GNP构成了一种有希望的非病毒siRNA载体,可用于改变MCF-7乳腺癌细胞中的基因表达,具有许多优势,例如相对较高的基因转染效率和有效的沉默能力。 (C)2016 Elsevier B.V.保留所有权利。

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