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Cited 19 time in webofscience Cited 18 time in scopus
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Long dsRNA-Mediated RNA Interference and Immunostimulation: A Targeted Delivery Approach Using Polyethyleneimine Based Nano-Carriers

Authors
Sajeesh, S[Sajeesh, S.]Lee, TY[Lee, Tae Yeon]Hong, SW[Hong, Sun Woo]Dua, P[Dua, Pooja]Choe, JY[Choe, Jeong Yong]Kang, A[Kang, Aeyeon]Yun, WS[Yun, Wan Soo]Song, C[Song, Changsik]Park, SH[Park, Sung Ha]Kim, S[Kim, Soyoun]Li, C[Li, Chiang]Lee, DK[Lee, Dong-Ki]
Issue Date
Mar-2014
Citation
MOLECULAR PHARMACEUTICS, v.11, no.3, pp.872 - 884
Indexed
SCIE
SCOPUS
Journal Title
MOLECULAR PHARMACEUTICS
Volume
11
Number
3
Start Page
872
End Page
884
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/53846
DOI
10.1021/mp400541z
ISSN
1543-8384
Abstract
RNA oligonucleotides Capable of inducing controlled immunostimulation combined with specific oncogene silencing via an RNA interference (RNAi) mechanism provide synergistic inhibition of cancer cell growth. With this concept, we previously designed a potent immunostimulatory long double stranded RNA, referred to as liRNA, capable of executing RNAi mediated specific target gene silencing. In this study, we developed a highly effective liRNA based targeted delivery system to apply in the treatment of glioblastoma multiforme. A stable nanocomplex was fabricated by complexing multimerized liRNA structures with cross-linked branched poly(ethylene imine) (bPEI) via electrostatic interactions. We show clear evidence that the cross-linked bPEI was quite effective in enhancing the cellular uptake of liRNA on U87MG cells. Moreover, the liRNA-PEI nanocomplex provided strong RNAi mediated target gene silencing compared to that of the conventional siRNA-PEI complex. Further, the bPEI modification strategy with specific ligand attachment assisted the uptake of the liRNA-PEI complex on the mouse brain endothelial cell line (b.End3). Such delivery systems combining the beneficial elements of targeted delivery, controlled immunostimulation, and RNAi mediated target silencing have immense potential in anticancer therapy.
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