4.7 Article Proceedings Paper

RNA Nanoparticle-Based Targeted Therapy for Glioblastoma through Inhibition of Oncogenic miR-21

Journal

MOLECULAR THERAPY
Volume 25, Issue 7, Pages 1544-1555

Publisher

CELL PRESS
DOI: 10.1016/j.ymthe.2016.11.016

Keywords

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Funding

  1. NIH [R35CA197706, U01CA151648, R01CA186100, R01NS064607, R01CA150153, P01CA163205, IRG-67-003-50, CA186542-01A1]
  2. DOD [W81XWH-15-1-0052]
  3. FACS [P30CA016058]

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Targeted inhibition of oncogenic miRNA-21 has been proposed to treat glioblastoma by rescuing tumor suppressors, PTEN and PDCD4. However, systemic delivery of anti-miR21 sequences requires a robust and efficient delivery platform to successfully inhibit this druggable target. Three-way junction (3WJ)-based RNA nanoparticles (RNP), artificially derived from pRNA of bacteriophage phi29 DNA packaging motor, was recently shown to target glioblastoma. Here, we report that multi-valent folate(FA)-conjugated 3WJ RNP constructed to harbor anti-miR-21 LNA sequences (FA-3WJ-LNA-miR21) specifically targeted and delivered anti-miR-21 LNA and knocked down miR-21 expression in glioblastoma cells in vitro and in vivo with favorable biodistribution. Systemically injected FA-3WJ-LNA-miR21 RNP efficiently rescued PTEN and PDCD4, resulting in glioblastoma cell apoptosis and tumor growth regression. Overall survival rate was also significantly improved by FA-3WJ-LNA-miR21 RNP. These results are indicative of the clinical benefit of FA-3WJ RNP-based gene therapy for the successful targeted therapy of developing and even recurring glioblastoma.

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