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Prostate cancer cell-specific VEGF siRNA delivery system using cell targeting peptide conjugated polyplexes

Authors
 Sun Hwa Kim  ;  Soo Hyeon Lee  ;  Huayu Tian  ;  Xuesi Chen  ;  Tae Gwan Park 
Citation
 JOURNAL OF DRUG TARGETING, Vol.17(4) : 311-317, 2009 
Journal Title
JOURNAL OF DRUG TARGETING
ISSN
 1061-186X 
Issue Date
2009
MeSH
Cell Line, Tumor ; Dose-Response Relationship, Drug ; Gene Silencing* ; Gene Targeting ; Gene Transfer Techniques ; Humans ; Ligands ; Male ; Microscopy, Confocal ; Polyethylene Glycols/chemistry ; Polyethyleneimine/chemistry ; Prostatic Neoplasms/genetics ; Prostatic Neoplasms/therapy* ; RNA, Small Interfering/administration & dosage* ; Vascular Endothelial Growth Factor A/genetics*
Keywords
Prostate cancer–targeted siRNA delivery system ; VEGF ; siRNA ; prostate cancer–binding peptide (PCP)
Abstract
A polymeric gene carrier was developed to deliver vascular endothelial growth factor (VEGF) small interfering RNA (siRNA) for prostate cancer cells in a target-specific manner. Prostate cancer-binding peptide (PCP) was conjugated with polyethylenimine (PEI) via a poly(ethylene glycol) (PEG) linker (PEI-PEG-PCP). The PEI-PEG-PCP conjugate could effectively condense siRNA to form stable polyelectrolyte complexes (polyplexes) with an average diameter of approximately 150 nm in an aqueous solution. VEGF siRNA/PEI-PEG-PCP polyplexes exhibited significantly higher VEGF inhibition efficiency than PCP-unmodified polycationic carriers (PEI-PEG or PEI) in human prostate carcinoma cells (PC-3 cells). The enhanced gene silencing activity of VEGF siRNA/PEI-PEG-PCP was maintained even under serum conditions, owing to the steric stabilization of the polyplexes with hydrophilic PEG grafts. Confocal microscopic studies revealed that the siRNA/PEI-PEG-PCP polyplexes were delivered into PC-3 cells in a PCP ligand-specific manner
Full Text
http://informahealthcare.com/doi/abs/10.1080/10611860902767232
DOI
10.1080/10611860902767232
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers
Yonsei Authors
Kim, Sun Hwa(김선화)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/105842
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