| Literature DB >> 30121212 |
Florian Gauthier1, Sandra Claveau2, Jean-Rémi Bertrand2, Jean-Jacques Vasseur1, Christelle Dupouy1, Françoise Debart3.
Abstract
Modified oligoribonucleotides used as siRNAs bearing biolabile disulfide-containing groups at some 2'-positions were synthesized following a post-synthesis transformation of solid-supported 2'-O-acetylthiomethyl RNA, previously described. Thus, the reduction-responsive and lipophilic benzyldithiomethyl (BnSSM) modification was introduced at different locations into siRNAs targeting the Ewing sarcoma EWS-Fli1 protein. Thermal stability, serum stability and response to glutathione treatment of modified siRNAs were thoroughly investigated. Among 17 modified siRNAs, significant gene silencing activities were demonstrated for the 8 most stable siRNAs in serum (half-life > 1 h) when using a transfection reagent. Of special interest, two naked 2'-O-BnSSM siRNAs transfection exhibited a remarkable gene silencing activity after 24 h incubation. These inhibitions are consistent with an efficient gymnotic delivery demonstrated by the presence of the corresponding fluorescent siRNAs within cells.Entities:
Keywords: Disulfide-containing groups; Gene silencing; Gymnotic delivery; Reduction-responsive; siRNA
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Year: 2018 PMID: 30121212 DOI: 10.1016/j.bmc.2018.07.033
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641