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Silencing disease genes in the laboratory and the clinic

The Journal of Pathology · 2011 · Vol. 226(2) · pp. 365–379
Jonathan K. WattsDavid R. Corey

Abstract

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.

MeSH terms

Cells, CulturedClinical Trials as TopicHumansResearch DesignProtein BiosynthesisGenetic TherapyOligonucleotides, AntisenseAlternative SplicingGene SilencingRNA, Small InterferingMicroRNAs

Funding

  • National Institutes of Health
  • Natural Sciences and Engineering Research Council of Canada
  • National Institute of General Medical Sciences
Citations
449
FWCI
9.71
field-weighted impact
References
191
Percentile
99%
vs. same field & year
Citations per year
Cited by
Antisense Oligonucleotides: An Emerging Area in Drug Discovery and Development
Journal of Clinical Medicine · 2020 · 516 citations
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