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

DC Field Value Language
dc.contributor.author김선화-
dc.date.accessioned2015-04-24T17:40:13Z-
dc.date.available2015-04-24T17:40:13Z-
dc.date.issued2009-
dc.identifier.issn1061-186X-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/105842-
dc.description.abstractA 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-
dc.description.statementOfResponsibilityopen-
dc.format.extent311~317-
dc.relation.isPartOfJOURNAL OF DRUG TARGETING-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHCell Line, Tumor-
dc.subject.MESHDose-Response Relationship, Drug-
dc.subject.MESHGene Silencing*-
dc.subject.MESHGene Targeting-
dc.subject.MESHGene Transfer Techniques-
dc.subject.MESHHumans-
dc.subject.MESHLigands-
dc.subject.MESHMale-
dc.subject.MESHMicroscopy, Confocal-
dc.subject.MESHPolyethylene Glycols/chemistry-
dc.subject.MESHPolyethyleneimine/chemistry-
dc.subject.MESHProstatic Neoplasms/genetics-
dc.subject.MESHProstatic Neoplasms/therapy*-
dc.subject.MESHRNA, Small Interfering/administration & dosage*-
dc.subject.MESHVascular Endothelial Growth Factor A/genetics*-
dc.titleProstate cancer cell-specific VEGF siRNA delivery system using cell targeting peptide conjugated polyplexes-
dc.typeArticle-
dc.contributor.collegeResearcher Institutes (부설 연구소)-
dc.contributor.departmentYonsei Integrative Research Institute for Cerebral & Cardiovascular Disease (뇌심혈관질환융합연구사업단)-
dc.contributor.googleauthorSun Hwa Kim-
dc.contributor.googleauthorSoo Hyeon Lee-
dc.contributor.googleauthorHuayu Tian-
dc.contributor.googleauthorXuesi Chen-
dc.contributor.googleauthorTae Gwan Park-
dc.identifier.doi10.1080/10611860902767232-
dc.admin.authorfalse-
dc.admin.mappingfalse-
dc.contributor.localIdA00561-
dc.relation.journalcodeJ01381-
dc.identifier.eissn1029-2330-
dc.identifier.pmid19242850-
dc.identifier.urlhttp://informahealthcare.com/doi/abs/10.1080/10611860902767232-
dc.subject.keywordProstate cancer–targeted siRNA delivery system-
dc.subject.keywordVEGF-
dc.subject.keywordsiRNA-
dc.subject.keywordprostate cancer–binding peptide (PCP)-
dc.contributor.alternativeNameKim, Sun Hwa-
dc.contributor.affiliatedAuthorKim, Sun Hwa-
dc.citation.volume17-
dc.citation.number4-
dc.citation.startPage311-
dc.citation.endPage317-
dc.identifier.bibliographicCitationJOURNAL OF DRUG TARGETING, Vol.17(4) : 311-317, 2009-
Appears in Collections:
1. College of Medicine (의과대학) > Research Institute (부설연구소) > 1. Journal Papers

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