Content area

Abstract

After nearly 40 years of development, oligonucleotide therapeutics are nearing meaningful clinical productivity. One of thekey advantages of oligonucleotide drugs is that their delivery and potency are derived primarily from the chemical structure of the oligonucleotide whereas their target is defined by the base sequence. Thus, as oligonucleotides with a particular chemical design show appropriate distribution and safety profiles for clinical gene silencing in a particular tissue, this will open the doorto the rapid development of additional drugs targeting other disease-associated genes in the same tissue. To achieve clinical productivity, the chemical architecture of the oligonucleotide needs to be optimized with a combination of sugar, backbone, nucleobase, and 3- and 5-terminal modifications. A portfolio of chemistries can be used to confer drug-like properties ontothe oligonucleotide as a whole, with minor chemical changes often translating into major improvements in clinical efficacy. One outstanding challenge in oligonucleotide chemical development is the optimization of chemical architectures to ensure long-term safety. There are multiple designs that enable effective targeting of the liver, but a second challenge is to develop designs that enable robust clinical efficacy in additional tissues.

Details

Title
The chemical evolution of oligonucleotide therapies of clinical utility
Author
Khvorova, Anastasia; Watts, Jonathan K
Pages
238-248
Publication year
2017
Publication date
Mar 2017
Publisher
Nature Publishing Group
ISSN
10870156
e-ISSN
15461696
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
1875116132
Copyright
Copyright Nature Publishing Group Mar 2017