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Small Drugs, Huge Impact: The Extraordinary Impact of Antisense Oligonucleotides in Research and Drug Development.
Quemener, Anais M; Centomo, Maria Laura; Sax, Scott L; Panella, Riccardo.
  • Quemener AM; University Rennes, CNRS, IGDR (Institute of Genetics and Development of Rennes)-UMR 6290, F-35000 Rennes, France.
  • Centomo ML; Department of Oncology, University of Turin, 10124 Turin, Italy.
  • Sax SL; Center for Genomic Medicine, Desert Research Institute, Reno, NV 89512, USA.
  • Panella R; Center for Genomic Medicine, Desert Research Institute, Reno, NV 89512, USA.
Molecules ; 27(2)2022 Jan 15.
Article in English | MEDLINE | ID: covidwho-1625662
ABSTRACT
Antisense oligonucleotides (ASOs) are an increasingly represented class of drugs. These small sequences of nucleotides are designed to precisely target other oligonucleotides, usually RNA species, and are modified to protect them from degradation by nucleases. Their specificity is due to their sequence, so it is possible to target any RNA sequence that is already known. These molecules are very versatile and adaptable given that their sequence and chemistry can be custom manufactured. Based on the chemistry being used, their activity may significantly change and their effects on cell function and phenotypes can differ dramatically. While some will cause the target RNA to decay, others will only bind to the target and act as a steric blocker. Their incredible versatility is the key to manipulating several aspects of nucleic acid function as well as their process, and alter the transcriptome profile of a specific cell type or tissue. For example, they can be used to modify splicing or mask specific sites on a target. The entire design rather than just the sequence is essential to ensuring the specificity of the ASO to its target. Thus, it is vitally important to ensure that the complete process of drug design and testing is taken into account. ASOs' adaptability is a considerable advantage, and over the past decades has allowed multiple new drugs to be approved. This, in turn, has had a significant and positive impact on patient lives. Given current challenges presented by the COVID-19 pandemic, it is necessary to find new therapeutic strategies that would complement the vaccination efforts being used across the globe. ASOs may be a very powerful tool that can be used to target the virus RNA and provide a therapeutic paradigm. The proof of the efficacy of ASOs as an anti-viral agent is long-standing, yet no molecule currently has FDA approval. The emergence and widespread use of RNA vaccines during this health crisis might provide an ideal opportunity to develop the first anti-viral ASOs on the market. In this review, we describe the story of ASOs, the different characteristics of their chemistry, and how their characteristics translate into research and as a clinical tool.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Oligonucleotides, Antisense / Drug Development Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Animals / Humans Country/Region as subject: North America Language: English Journal subject: Biology Year: 2022 Document Type: Article Affiliation country: Molecules27020536

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Oligonucleotides, Antisense / Drug Development Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Animals / Humans Country/Region as subject: North America Language: English Journal subject: Biology Year: 2022 Document Type: Article Affiliation country: Molecules27020536