靶向递送siRNA治疗恶性肿瘤。

Journal of drug delivery Pub Date : 2017-01-01 Epub Date: 2017-11-09 DOI:10.1155/2017/6971297
Qixin Leng, Martin C Woodle, A James Mixson
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引用次数: 16

摘要

在过去的20年里,已经发现了一组不同的靶向表面生物标志物或受体的配体,其中一些研究将siRNA靶向肿瘤。利用噬菌体展示、体外进化和重组抗体等方法开发肿瘤归甲肽、RNA和DNA适体以及单链可变片段抗体的许多方法在20世纪80年代的研究人员是无法想象的。尽管有这么多的科学进步,但没有理由认为配体领域不会继续发展。从基于新型或现有生物标志物的配体的开发,到将配体与药物、基因和反义传递系统连接,几个领域已经结合起来,以促进配体导向的siRNA治疗。在这篇综述中,我们讨论了针对配体的siRNA治疗肿瘤的主要类别,以及识别新配体的不同策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targeted Delivery of siRNA Therapeutics to Malignant Tumors.

Targeted Delivery of siRNA Therapeutics to Malignant Tumors.

Targeted Delivery of siRNA Therapeutics to Malignant Tumors.

Targeted Delivery of siRNA Therapeutics to Malignant Tumors.

Over the past 20 years, a diverse group of ligands targeting surface biomarkers or receptors has been identified with several investigated to target siRNA to tumors. Many approaches to developing tumor-homing peptides, RNA and DNA aptamers, and single-chain variable fragment antibodies by using phage display, in vitro evolution, and recombinant antibody methods could not have been imagined by researchers in the 1980s. Despite these many scientific advances, there is no reason to expect that the ligand field will not continue to evolve. From development of ligands based on novel or existing biomarkers to linking ligands to drugs and gene and antisense delivery systems, several fields have coalesced to facilitate ligand-directed siRNA therapeutics. In this review, we discuss the major categories of ligand-targeted siRNA therapeutics for tumors, as well as the different strategies to identify new ligands.

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来源期刊
Journal of drug delivery
Journal of drug delivery PHARMACOLOGY & PHARMACY-
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