
Mesyl phosphoramidate backbone modified antisense oligonucleotides targeting miR-21 with enhanced in vivo therapeutic potency
Author(s) -
Olga Patutina,
Svetlana Gaponova,
Aleksandra V. Sen’kova,
Innokenty A. Savin,
Daniil V. Gladkikh,
Е. А. Буракова,
А. А. Фокина,
М. А. Маслов,
Elena V. Shmendel,
Mattew J. A. Wood,
Valentin V. Vlassov,
Sidney Altman,
Dmitry A. Stetsenko,
М. А. Зенкова
Publication year - 2020
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.2016158117
Subject(s) - oligonucleotide , phosphoramidate , in vivo , in vitro , nuclease , biology , rnase p , microrna , rna , rnase h , carcinogenesis , biochemistry , microbiology and biotechnology , cancer research , chemistry , gene , genetics
The design of modified oligonucleotides that combine in one molecule several therapeutically beneficial properties still poses a major challenge. Recently a new type of modified mesyl phosphoramidate (or µ-) oligonucleotide was described that demonstrates high affinity to RNA, exceptional nuclease resistance, efficient recruitment of RNase H, and potent inhibition of key carcinogenesis processes in vitro. Herein, using a xenograft mouse tumor model, it was demonstrated that microRNA miR-21-targeted µ-oligonucleotides administered in complex with folate-containing liposomes dramatically inhibit primary tumor growth via long-term down-regulation of miR-21 in tumors and increase in biosynthesis of miR-21-regulated tumor suppressor proteins. This antitumoral effect is superior to the effect of the corresponding phosphorothioate. Peritumoral administration of µ-oligonucleotide results in its rapid distribution and efficient accumulation in the tumor. Blood biochemistry and morphometric studies of internal organs revealed no pronounced toxicity of µ-oligonucleotides. This new oligonucleotide class provides a powerful tool for antisense technology.