Nanoscale polyelectrolyte complexes encapsulating mRNA and long-chained siRNA for combinatorial cancer gene therapy
- Authors
- Kim, Myung Goo; Jo, Sung Duk; Jeong, Ji Hoon; Kim, Sun Hwa
- Issue Date
- 2018-08
- Publisher
- 한국공업화학회
- Citation
- Journal of Industrial and Engineering Chemistry, v.64, pp.430 - 437
- Abstract
- To precisely regulate target genes that are abnormally expressed in cancers, we suggest an RNA-mediated multigene targeting system that co-encapsulates siRNA against vascular endothelial growth factor (VEGF) and mRNA encoding phosphatase and tensin homolog (PTEN). Polymerized long-chain siRNAs (L-siRNAs) formed stable and condensed nanocomplexes with mRNAs using thiolated glycol chitosans (tGCs) as gene carriers. The mRNA/L-siRNA/tGC nanocomplexes (MSNs) exhibited efficient intracellular delivery and superior anti-tumor efficiency with simultaneous up and down-regulation of PTEN and VEGF, respectively. The MSN system can be considered as a new platform for cancer gene therapy requiring accurate control of multiple gene expressions. (C) 2018 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
- Keywords
- GLYCOL CHITOSAN NANOPARTICLES; DELIVERY-SYSTEMS; PERSISTENCE LENGTH; NONVIRAL VECTORS; CELLULAR UPTAKE; STRANDED RNA; THERAPEUTICS; STABILITY; VEGF; DNA; Gene therapy; siRNA; mRNA; Polyelectrolyte complex
- ISSN
- 1226-086X
- URI
- https://pubs.kist.re.kr/handle/201004/121067
- DOI
- 10.1016/j.jiec.2018.04.005
- Appears in Collections:
- KIST Article > 2018
- Files in This Item:
There are no files associated with this item.
- Export
- RIS (EndNote)
- XLS (Excel)
- XML
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.