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

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dc.contributor.authorKim, Sun Hwako
dc.contributor.authorLee, Soo Hyeonko
dc.contributor.authorTian, Huayuko
dc.contributor.authorChen, Xuesiko
dc.contributor.authorPark, Tae Gwanko
dc.date.accessioned2009-11-23T06:10:20Z-
dc.date.available2009-11-23T06:10:20Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-05-
dc.identifier.citationJOURNAL OF DRUG TARGETING, v.17, no.4, pp.311 - 317-
dc.identifier.issn1061-186X-
dc.identifier.urihttp://hdl.handle.net/10203/13118-
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.sponsorshipthe grant (F104AA010002- 07A0101-00210) and A3 project from the Ministry of Education, Science and Technology, Republic of Korea.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherINFORMA HEALTHCARE-
dc.subjectPOLYELECTROLYTE COMPLEX MICELLES-
dc.subjectMEDIATED DELIVERY-
dc.subjectRNA INTERFERENCE-
dc.subjectGENE DELIVERY-
dc.subjectPLASMID DNA-
dc.subjectGLYCOL)-
dc.subjectTHERAPY-
dc.subjectGROWTH-
dc.subjectCOPOLYMERS-
dc.subjectPEI-
dc.titleProstate cancer cell-specific VEGF siRNA delivery system using cell targeting peptide conjugated polyplexes-
dc.typeArticle-
dc.identifier.wosid000266593800007-
dc.identifier.scopusid2-s2.0-70349536942-
dc.type.rimsART-
dc.citation.volume17-
dc.citation.issue4-
dc.citation.beginningpage311-
dc.citation.endingpage317-
dc.citation.publicationnameJOURNAL OF DRUG TARGETING-
dc.identifier.doi10.1080/10611860902767232-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorPark, Tae Gwan-
dc.contributor.nonIdAuthorKim, Sun Hwa-
dc.contributor.nonIdAuthorLee, Soo Hyeon-
dc.contributor.nonIdAuthorTian, Huayu-
dc.contributor.nonIdAuthorChen, Xuesi-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorProstate cancer-targeted siRNA delivery system-
dc.subject.keywordAuthorVEGF-
dc.subject.keywordAuthorsiRNA-
dc.subject.keywordAuthorprostate cancer-binding peptide (PCP)-
dc.subject.keywordPlusPOLYELECTROLYTE COMPLEX MICELLES-
dc.subject.keywordPlusMEDIATED DELIVERY-
dc.subject.keywordPlusRNA INTERFERENCE-
dc.subject.keywordPlusGENE DELIVERY-
dc.subject.keywordPlusPLASMID DNA-
dc.subject.keywordPlusGLYCOL)-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusCOPOLYMERS-
dc.subject.keywordPlusPEI-
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