Catalytic Knockdown of miR-21 by Artificial Ribonuclease: Biological Performance in Tumor Model.
Ontology highlight
ABSTRACT: Control of the expression of oncogenic small non-coding RNAs, notably microRNAs (miRNAs), is an attractive therapeutic approach. We report a design platform for catalytic knockdown of miRNA targets with artificial, sequence-specific ribonucleases. miRNases comprise a peptide [(LeuArg)2Gly]2 capable of RNA cleavage conjugated to the miRNA-targeted oligodeoxyribonucleotide, which becomes nuclease-resistant within the conjugate design, without resort to chemically modified nucleotides. Our data presented here showed for the first time a truly catalytic character of our miR-21-miRNase and its ability to cleave miR-21 in a multiple catalytic turnover mode. We demonstrate that miRNase targeted to miR-21 (miR-21-miRNase) knocked down malignant behavior of tumor cells, includ
SUBMITTER: Patutina OA
PROVIDER: S-EPMC6698794 | biostudies-literature | 2019
REPOSITORIES: biostudies-literature
ACCESS DATA