Therapeutic Antisense Oligonucleotides Are Coming of Age

被引:409
作者
Bennett, C. Frank [1 ]
机构
[1] Ionis Pharmaceut, Carlsbad, CA 92010 USA
来源
ANNUAL REVIEW OF MEDICINE, VOL 70 | 2019年 / 70卷
关键词
antisense oligonucleotides; eteplirsen; inotersen; nusinersen; patisiran; RNA interference; RNA splicing; siRNA; DUCHENNE MUSCULAR-DYSTROPHY; MOLECULAR-MECHANISMS; RNAI THERAPEUTICS; MESSENGER-RNAS; SHAM CONTROL; OPEN-LABEL; IN-VIVO; NUSINERSEN; ETEPLIRSEN; TRANSLATION;
D O I
10.1146/annurev-med-041217-010829
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The first published description of therapeutic applications of antisense oligonucleotide (ASO) technology occurred in the late 1970s and was followed by the founding of commercial companies focused on developing antisense therapeutics in the late 1980s. Since the late 1980s, there has been steady progress in improving the technology platform, taking advantage of advances in oligonucleotide chemistry and formulations as well as increased understanding of the distribution and safety of ASOs. There are several approved ASO drugs and a broad pipeline in development. In addition, advances in understanding human disease, including the genetic basis for most monogenic diseases and the availability of the full human genome sequence, have created numerous therapeutic applications for the technology. I summarize the state of the technology and highlight how advances in the technology position ASOs to be an important contributor to future medicines.
引用
收藏
页码:307 / 321
页数:15
相关论文
共 74 条
[41]  
Khvorova A, 2003, CELL, V115, P209, DOI 10.1016/S0092-8674(03)00801-8
[42]  
Kinali M, 2009, LANCET NEUROL, V8, P918, DOI 10.1016/S1474-4422(09)70211-X
[43]   Mechanisms of single-stranded phosphorothioate modified antisense oligonucleotide accumulation in hepatocytes [J].
Koller, Erich ;
Vincent, Thomas M. ;
Chappell, Alfred ;
De, Soma ;
Manoharan, Muthiah ;
Bennett, C. Frank .
NUCLEIC ACIDS RESEARCH, 2011, 39 (11) :4795-4807
[44]   Silencing of microRNAs in vivo with 'antagomirs' [J].
Krützfeldt, J ;
Rajewsky, N ;
Braich, R ;
Rajeev, KG ;
Tuschl, T ;
Manoharan, M ;
Stoffel, M .
NATURE, 2005, 438 (7068) :685-689
[45]   Chemical and structural modifications of RNAi therapeutics [J].
Ku, Sook Hee ;
Jo, Sung Duk ;
Lee, Yeon Kyung ;
Kim, Kwangmeyung ;
Kim, Sun Hwa .
ADVANCED DRUG DELIVERY REVIEWS, 2016, 104 :16-28
[46]   Lipid Nanoparticles for Short Interfering RNA Delivery [J].
Leung, Alex K. K. ;
Tam, Yuen Yi C. ;
Cullis, Pieter R. .
NONVIRAL VECTORS FOR GENE THERAPY LIPID- AND POLYMER-BASED GENE TRANSFER, 2014, 88 :71-110
[47]   Antisense oligonucleotides targeting translation inhibitory elements in 5′ UTRs can selectively increase protein levels [J].
Liang, Xue-hai ;
Sun, Hong ;
Shen, Wen ;
Wang, Shiyu ;
Yao, Joyee ;
Migawa, Michael T. ;
Huynh-Hoa Bui ;
Damle, Sagar S. ;
Riney, Stan ;
Graham, Mark J. ;
Crooke, Rosanne M. ;
Crooke, Stanley T. .
NUCLEIC ACIDS RESEARCH, 2017, 45 (16) :9528-9546
[48]   Translation efficiency of mRNAs is increased by antisense oligonucleotides targeting upstream open reading frames [J].
Liang, Xue-hai ;
Shen, Wen ;
Sun, Hong ;
Migawa, Michael T. ;
Vickers, Timothy A. ;
Crooke, Stanley T. .
NATURE BIOTECHNOLOGY, 2016, 34 (08) :875-+
[49]   Viable RNaseH1 knockout mice show RNaseH1 is essential for R loop processing, mitochondrial and liver function [J].
Lima, Walt F. ;
Murray, Heather M. ;
Damle, Sagar S. ;
Hart, Christopher E. ;
Hung, Gene ;
De Hoyos, Cheryl Li ;
Liang, Xue-Hai ;
Crooke, Stanley T. .
NUCLEIC ACIDS RESEARCH, 2016, 44 (11) :5299-5312
[50]   DE-NOVO AND INHERITED DELETIONS OF THE 5Q13 REGION IN SPINAL MUSCULAR ATROPHIES [J].
MELKI, J ;
LEFEBVRE, S ;
BURGLEN, L ;
BURLET, P ;
CLERMONT, O ;
MILLASSEAU, P ;
REBOULLET, S ;
BENICHOU, B ;
ZEVIANI, M ;
LEPASLIER, D ;
COHEN, D ;
WEISSENBACH, J ;
MUNNICH, A .
SCIENCE, 1994, 264 (5164) :1474-1477