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长双链RNA介导的RNA干扰和免疫刺激:一种使用基于聚乙烯亚胺的纳米载体的靶向递送方法。

Long dsRNA-mediated RNA interference and immunostimulation: a targeted delivery approach using polyethyleneimine based nano-carriers.

作者信息

Sajeesh S, Lee Tae Yeon, Hong Sun Woo, Dua Pooja, Choe Jeong Yong, Kang Aeyeon, Yun Wan Soo, Song Changsik, Park Sung Ha, Kim Soyoun, Li Chiang, Lee Dong-Ki

机构信息

Global Research Laboratory for RNAi Medicine, Department of Chemistry, Sungkyunkwan University , Suwon 440-746, Republic of Korea.

出版信息

Mol Pharm. 2014 Mar 3;11(3):872-84. doi: 10.1021/mp400541z. Epub 2014 Feb 20.

Abstract

RNA oligonucleotides capable of inducing controlled immunostimulation combined with specific oncogene silencing via an RNA interference (RNAi) mechanism provide synergistic inhibition of cancer cell growth. With this concept, we previously designed a potent immunostimulatory long double stranded RNA, referred to as liRNA, capable of executing RNAi mediated specific target gene silencing. In this study, we developed a highly effective liRNA based targeted delivery system to apply in the treatment of glioblastoma multiforme. A stable nanocomplex was fabricated by complexing multimerized liRNA structures with cross-linked branched poly(ethylene imine) (bPEI) via electrostatic interactions. We show clear evidence that the cross-linked bPEI was quite effective in enhancing the cellular uptake of liRNA on U87MG cells. Moreover, the liRNA-PEI nanocomplex provided strong RNAi mediated target gene silencing compared to that of the conventional siRNA-PEI complex. Further, the bPEI modification strategy with specific ligand attachment assisted the uptake of the liRNA-PEI complex on the mouse brain endothelial cell line (b.End3). Such delivery systems combining the beneficial elements of targeted delivery, controlled immunostimulation, and RNAi mediated target silencing have immense potential in anticancer therapy.

摘要

能够通过RNA干扰(RNAi)机制诱导可控免疫刺激并结合特定癌基因沉默的RNA寡核苷酸可协同抑制癌细胞生长。基于这一概念,我们之前设计了一种强效的免疫刺激长双链RNA,称为liRNA,它能够执行RNAi介导的特定靶基因沉默。在本研究中,我们开发了一种基于liRNA的高效靶向递送系统,用于治疗多形性胶质母细胞瘤。通过静电相互作用将多聚化的liRNA结构与交联支化聚(乙烯亚胺)(bPEI)复合,制备了一种稳定的纳米复合物。我们有明确的证据表明,交联的bPEI在增强U87MG细胞对liRNA的细胞摄取方面非常有效。此外,与传统的siRNA-PEI复合物相比,liRNA-PEI纳米复合物提供了更强的RNAi介导的靶基因沉默。此外,具有特定配体附着的bPEI修饰策略有助于liRNA-PEI复合物在小鼠脑内皮细胞系(b.End3)上的摄取。这种结合了靶向递送、可控免疫刺激和RNAi介导的靶沉默等有益元素的递送系统在抗癌治疗中具有巨大潜力。

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