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dc.contributor.authorShali, H
dc.contributor.authorShabani, M
dc.contributor.authorPourgholi, F
dc.contributor.authorHajivalili, M
dc.contributor.authorAghebati-Maleki, L
dc.contributor.authorJadidi-Niaragh, F
dc.contributor.authorBaradaran, B
dc.contributor.authorAkbari, AAM
dc.contributor.authorYounesi, V
dc.contributor.authorYousefi, M
dc.date.accessioned2018-08-26T07:13:12Z
dc.date.available2018-08-26T07:13:12Z
dc.date.issued2018
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44904
dc.description.abstractHere, we investigated the effects of dual delivery of IGF-1R siRNA and doxorubicin by chitosan nanoparticles on viability of A549 lung cancer cells line by utilization of MTT and qRT-PCR. Furthermore apoptosis and migration of treated cells were assessed by Annexin-PI and wound healing assays, respectively. The chitosan nanoparticles had about 176nm size with zeta potential and polydispersive index about 11mV and 0.3, respectively. The IGF-1R siRNA had synergistic effect on DOX-induced cytotoxicity and apoptosis in tumour cells. In addition, siRNA/DOX-loaded chitosan nanoparticles could significantly decrease migration and expressions of mmp9, VEGF and STAT3 in A549 cells.
dc.language.isoEnglish
dc.relation.ispartofARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY
dc.subjectChitosan nanoparticle
dc.subjectdoxorubicin
dc.subjectIGF-1R
dc.subjectlung cancer
dc.subjectss siRNA
dc.titleCo-delivery of insulin-like growth factor 1 receptor specific siRNA and doxorubicin using chitosan-based nanoparticles enhanced anticancer efficacy in A549 lung cancer cell line
dc.typeArticle
dc.citation.volume46
dc.citation.issue2
dc.citation.spage293
dc.citation.epage302
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1080/21691401.2017.1307212


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