Publication: Investigation of the Therapeutic Efficacy of Codelivery of psiRNA-Vascular Endothelial Growth Factor and pIL-4 into Chitosan Nanoparticles in the Breast Tumor Model
dc.contributor.author | EREN, FATİH | |
dc.contributor.authors | Salva, Emine; Turan, Suna O.; Kabasakal, Levent; Alan, Saadet; Ozkan, Naziye; Eren, Fatih; Akbuga, Julide | |
dc.date.accessioned | 2022-03-13T12:46:34Z | |
dc.date.available | 2022-03-13T12:46:34Z | |
dc.date.issued | 2014 | |
dc.description.abstract | Angiogenesis has been known to increase tumor growth and for its metastatic potential in human tumors. Vascular endothelial growth factor (VEGF) plays an important role in tumor angiogenesis and is a promising therapeutic target for breast cancer. VEGF is an essential target for RNAi-based gene therapy of breast cancer. Interleukin-4 (IL-4) may act as an anti-angiogenic molecule that inhibits tumor growth and migration in rats. The purpose of the present study was to improve therapeutic efficacy in breast cancer with the codelivery of siRNA-expressing plasmid targeting VEGF and IL-4-expressing plasmid encapsulating into chitosan nanoparticles (NPs). The codelivery of psiVEGF and pIL-4 plasmids greatly enhanced in vitro and in vivo gene-silencing efficiency. For the in vitro study, when psiVEGF and pIL-4 into chitosan NPs were combined (81%), the gene-silencing effect was higher than psiVEGF and pIL-4 NPs alone. The in vivo study breast tumor model demonstrated that the administration of coencapsulation of psiVEGF and pIL-4 into chitosan NPs caused an additive effect on breast tumor growth inhibition (97%), compared with containing NPs psiVEGF or pIL-4 alone. These results indicate that chitosan NPs can be effectively used for the codelivery of pIL-4 and siVEGF-expressing plasmid in a combination therapy against breast cancer. (c) 2013 Wiley Periodicals, Inc. | |
dc.identifier.doi | 10.1002/jps.23815 | |
dc.identifier.eissn | 1520-6017 | |
dc.identifier.issn | 0022-3549 | |
dc.identifier.pubmed | 24357345 | |
dc.identifier.uri | https://hdl.handle.net/11424/237942 | |
dc.identifier.wos | WOS:000331392900002 | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER SCIENCE INC | |
dc.relation.ispartof | JOURNAL OF PHARMACEUTICAL SCIENCES | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | RNA interference | |
dc.subject | VEGF | |
dc.subject | IL-4 | |
dc.subject | chitosan nanoparticles | |
dc.subject | breast cancer | |
dc.subject | SIRNA DELIVERY | |
dc.subject | RNA INTERFERENCE | |
dc.subject | PLASMID DNA | |
dc.subject | INTERLEUKIN-4 | |
dc.subject | ANGIOGENESIS | |
dc.subject | EXPRESSION | |
dc.subject | POLYMORPHISM | |
dc.subject | INHIBITION | |
dc.subject | COMPLEXES | |
dc.subject | CARRIER | |
dc.title | Investigation of the Therapeutic Efficacy of Codelivery of psiRNA-Vascular Endothelial Growth Factor and pIL-4 into Chitosan Nanoparticles in the Breast Tumor Model | |
dc.type | article | |
dspace.entity.type | Publication | |
local.avesis.id | f9056023-3d2e-4132-90b5-06fb29e2261d | |
local.import.package | SS17 | |
local.indexed.at | WOS | |
local.indexed.at | SCOPUS | |
local.journal.numberofpages | 11 | |
oaire.citation.endPage | 795 | |
oaire.citation.issue | 3 | |
oaire.citation.startPage | 785 | |
oaire.citation.title | JOURNAL OF PHARMACEUTICAL SCIENCES | |
oaire.citation.volume | 103 | |
relation.isAuthorOfPublication | 4bc77d63-5aa7-4c67-8d60-12778ea963b1 | |
relation.isAuthorOfPublication.latestForDiscovery | 4bc77d63-5aa7-4c67-8d60-12778ea963b1 |