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基于 RNAi 的治疗方法——现状、挑战与展望。

RNAi-based therapeutics-current status, challenges and prospects.

机构信息

Department of Molecular Biology, Beckman Research Institute of the City of Hope, Duarte, CA, USA.

出版信息

EMBO Mol Med. 2009 Jun;1(3):142-51. doi: 10.1002/emmm.200900023.


DOI:10.1002/emmm.200900023
PMID:20049714
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3378126/
Abstract

RNA interference (RNAi) is a collection of small RNA directed mechanisms that result in sequence specific inhibition of gene expression. The notion that RNAi could lead to a new class of therapeutics caught the attention of many investigators soon after its discovery. The field of applied RNAi therapeutics has moved very quickly from lab to bedside. The RNAi approach has been widely used for drug development and several phase I and II clinical trials are under way. However, there are still some concerns and challenges to overcome for therapeutic applications. These include the potential for off-target effects, triggering innate immune responses and most importantly obtaining specific delivery into the cytoplasm of target cells. This review focuses on the current status of RNAi-based therapeutics, the challenges it faces and how to overcome them.

摘要

RNA 干扰(RNAi)是一组由小 RNA 指导的机制,导致基因表达的序列特异性抑制。RNAi 可能导致一类新的治疗药物的概念在发现后不久就引起了许多研究人员的关注。应用 RNAi 治疗学领域已经从实验室迅速发展到临床。RNAi 方法已广泛用于药物开发,并且正在进行几项 I 期和 II 期临床试验。然而,对于治疗应用仍然存在一些需要克服的问题和挑战。这些包括潜在的脱靶效应、触发先天免疫反应,以及最重要的是获得特定的递送到靶细胞的细胞质。这篇综述重点介绍了基于 RNAi 的治疗方法的现状、面临的挑战以及如何克服这些挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/3378126/a8f961ae16b6/emmm0001-0142-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/3378126/5940f616eabe/emmm0001-0142-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/3378126/a8f961ae16b6/emmm0001-0142-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/3378126/5940f616eabe/emmm0001-0142-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faba/3378126/a8f961ae16b6/emmm0001-0142-f2.jpg

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本文引用的文献

[1]
Nanotechnology approach for drug addiction therapy: gene silencing using delivery of gold nanorod-siRNA nanoplex in dopaminergic neurons.

Proc Natl Acad Sci U S A. 2009-4-7

[2]
Overexpression of RRM2 decreases thrombspondin-1 and increases VEGF production in human cancer cells in vitro and in vivo: implication of RRM2 in angiogenesis.

Mol Cancer. 2009-2-28

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Therapeutic siRNAs for dominant genetic skin disorders including pachyonychia congenita.

J Dermatol Sci. 2008-9

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