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治疗性核酸:当前临床状况

Therapeutic nucleic acids: current clinical status.

作者信息

Sridharan Kannan, Gogtay Nithya Jaideep

机构信息

Department of Health Sciences, College of Medicine, Nursing and Health Sciences, Fiji National University, Suva, Fiji.

Department of Clinical Pharmacology, Seth GS Medical College and KEM Hospital, Mumbai, India.

出版信息

Br J Clin Pharmacol. 2016 Sep;82(3):659-72. doi: 10.1111/bcp.12987. Epub 2016 Jun 3.

Abstract

Deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) are simple linear polymers that have been the subject of considerable research in the last two decades and have now moved into the realm of being stand-alone therapeutic agents. Much of this has stemmed from the appreciation that they carry out myriad functions that go beyond mere storage of genetic information and protein synthesis. Therapy with nucleic acids either uses unmodified DNA or RNA or closely related compounds. From both a development and regulatory perspective, they fall somewhere between small molecules and biologics. Several of these compounds are in clinical development and many have received regulatory approval for human use. This review addresses therapeutic uses of DNA based on antisense oligonucleotides, DNA aptamers and gene therapy; and therapeutic uses of RNA including micro RNAs, short interfering RNAs, ribozymes, RNA decoys and circular RNAs. With their specificity, functional diversity and limited toxicity, therapeutic nucleic acids hold enormous promise. However, challenges that need to be addressed include targeted delivery, mass production at low cost, sustaining efficacy and minimizing off-target toxicity. Technological developments will hold the key to this and help accelerate drug approvals in the years to come.

摘要

脱氧核糖核酸(DNA)和核糖核酸(RNA)是简单的线性聚合物,在过去二十年中一直是大量研究的主题,如今已进入独立治疗剂的领域。这很大程度上源于人们认识到它们执行着众多功能,不仅仅是储存遗传信息和蛋白质合成。核酸治疗要么使用未修饰的DNA或RNA,要么使用密切相关的化合物。从研发和监管的角度来看,它们处于小分子和生物制品之间。其中几种化合物正在进行临床开发,许多已获得人类使用的监管批准。本综述探讨了基于反义寡核苷酸、DNA适体和基因治疗的DNA治疗用途;以及RNA的治疗用途,包括微小RNA、小干扰RNA、核酶、RNA诱饵和环状RNA。治疗性核酸因其特异性、功能多样性和有限的毒性而具有巨大的潜力。然而,需要解决的挑战包括靶向递送、低成本大规模生产、维持疗效以及将脱靶毒性降至最低。技术发展将是关键,并有助于在未来几年加速药物批准。

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