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金纳米颗粒辅助短发夹 RNA 递送抑制 Mcl-1L 对小鼠异种移植肿瘤生长的作用。

Inhibition of xenograft tumor growth in mice by gold nanoparticle-assisted delivery of short hairpin RNAs against Mcl-1L.

机构信息

Department of Pharmacy, College of Pharmacy, CHA University, Seongnam 463-836, Republic of Korea.

出版信息

J Biotechnol. 2011 Nov 10;156(2):89-94. doi: 10.1016/j.jbiotec.2011.07.037. Epub 2011 Aug 31.

Abstract

A prerequisite for the therapeutic use of small RNAs is the development of a method that can deliver them into animals. Previous studies have shown the capability of functionalized gold nanoparticles to serve as a general platform for loading and delivering DNA oligonucleotides and short hairpin RNAs (shRNAs) into cultured human cells. Here, we report the ability of the gold nanoparticle-assisted gene delivery system (AuNP-GDS) to deliver shRNA to a xenograft tumor in a mouse model. AuNP-GDS delivery of in vitro synthesized shRNA targeted to the Mcl-1L gene knocked down levels of Mcl-1L mRNA and protein by ~36% and ~26%, respectively, which were sufficient to induce apoptosis of the xenograft tumor cells and consequently inhibited the development of the tumor. We demonstrated that our lego-like AuNP-GDS, which can easily load and deliver shRNAs targeted to any gene of interest into living systems, can deliver shRNAs into xenograft tumors, leading to antitumor activity in an animal model.

摘要

治疗性使用小 RNA 的前提是开发一种能够将它们递送到动物体内的方法。先前的研究表明,功能化金纳米粒子能够作为一种通用平台,用于将 DNA 寡核苷酸和短发夹 RNA(shRNA)加载和递送至培养的人类细胞。在这里,我们报告了金纳米粒子辅助基因传递系统(AuNP-GDS)将 shRNA 递送至小鼠模型中的异种移植肿瘤的能力。AuNP-GDS 递送体外合成的针对 Mcl-1L 基因的 shRNA,使 Mcl-1L mRNA 和蛋白质的水平分别降低了约 36%和 26%,足以诱导异种移植肿瘤细胞凋亡,并因此抑制肿瘤的发展。我们证明了我们的类似乐高的 AuNP-GDS,可以轻松地将针对任何感兴趣基因的 shRNA 加载并递送至活体系统中,能够将 shRNA 递送至异种移植肿瘤中,从而在动物模型中产生抗肿瘤活性。

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