Silencing disease genes in the laboratory and the clinic

被引:373
作者
Watts, Jonathan K.
Corey, David R. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Biochem, Dallas, TX 75390 USA
基金
美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
antisense oligonucleotides; siRNA; mRNA; gene silencing; therapeutics; LOCKED NUCLEIC-ACID; MEDIATE RNA INTERFERENCE; IN-VIVO DELIVERY; ANTISENSE OLIGONUCLEOTIDES; MESSENGER-RNA; CHEMICAL-MODIFICATION; DYSTROPHIN EXPRESSION; RATIONAL DESIGN; LDL CHOLESTEROL; ERYTHROID-CELLS;
D O I
10.1002/path.2993
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Synthetic nucleic acids are commonly used laboratory tools for modulating gene expression and have the potential to be widely used in the clinic. Progress towards nucleic acid drugs, however, has been slow and many challenges remain to be overcome before their full impact on patient care can be understood. Antisense oligonucleotides (ASOs) and small interfering RNAs (siRNAs) are the two most widely used strategies for silencing gene expression. We first describe these two approaches and contrast their relative strengths and weaknesses for laboratory applications. We then review the choices faced during development of clinical candidates and the current state of clinical trials. Attitudes towards clinical development of nucleic acid silencing strategies have repeatedly swung from optimism to depression during the past 20 years. Our goal is to provide the information needed to design robust studies with oligonucleotides, making use of the strengths of each oligonucleotide technology. Copyright (C) 2011 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:365 / 379
页数:15
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