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Development of Antibody-Oligonucleotide Complexes for Targeting Exosomal MicroRNA.

Asako YamayoshiShota OyamaYusuke KishimotoRyo KonishiTsuyoshi YamamotoAkio KoboriHiroshi HaradaEishi AshiharaHiroshi SugiyamaAkira Murakami
Published in: Pharmaceutics (2020)
MicroRNAs in exosomes (exosomal miRNAs) are considered as significant targets for cancer therapy. Anti-miR oligonucleotides are often used for the functional inhibition of miRNAs; however, there are no studies regarding the regulation of exosomal miRNA functions. In this study, we attempted to develop a novel drug delivery system using anti-exosome antibody-anti-miR oligonucleotide complexes (ExomiR-Tracker) to hijack exosomes to carry anti-miR oligonucleotides inside exosome-recipient cells. We found that ExomiR-Tracker bound to the exosomes, and then the complexes were introduced into the recipient cells. We also found that anti-miR oligonucleotides introduced into the recipient cells can exhibit inhibitory effects on exosomal miRNA functions in vitro and in vivo. We believe that our strategy would be a promising one for targeting exosomal miRNAs.
Keyphrases
  • induced apoptosis
  • cell proliferation
  • long non coding rna
  • cancer therapy
  • cell cycle arrest
  • long noncoding rna
  • stem cells
  • mesenchymal stem cells
  • endoplasmic reticulum stress
  • signaling pathway
  • cell death
  • pi k akt