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dc.contributor.authorFekri Aval, S
dc.contributor.authorAkbarzadeh, A
dc.contributor.authorYamchi, MR
dc.contributor.authorZarghami, F
dc.contributor.authorNejati-Koshki, K
dc.contributor.authorZarghami, N
dc.date.accessioned2018-08-26T06:04:45Z
dc.date.available2018-08-26T06:04:45Z
dc.date.issued2016
dc.identifier10.3109/21691401.2014.934456
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41565
dc.description.abstractTelomerase is expressed in most of malignant cells, including lung cancer cells. The success of small interfering RNA (siRNA) in silencing of the telomerase catalytic subunit depends upon carriers ability to efficiently deliver therapeutic agent to cells with minimal toxicity and most biocompatibility. In this study, a potential carrier for efficient delivery was assessed by siRNA encapsulating into Iron MNPs modified with biodegradable polyester nanoparticles consisting of PLGA and PEG.Data analysis shows that the self-assemble diblock copolymers were synthesized, and then the siRNA designed against hTERT catalytic subunit was encapsulated. Also, the rate of telomerase gene expression in equivalent with magnetic copolymers/siRNA was lower than that of free siRNA (P = 0.001).In conclusion, regarding the enhancing of siRNA stability by magnetic copolymer, the expression of telomerase gene was significantly lower in the cells treated with siRNA-magnetic copolymers than those treated with free siRNA.
dc.language.isoEnglish
dc.relation.ispartofArtificial cells, nanomedicine, and biotechnology
dc.subjectCell Line, Tumor
dc.subjectCell Survival
dc.subjectDrug Carriers
dc.subjectEpithelial Cells
dc.subjectFerrosoferric Oxide
dc.subjectGene Expression
dc.subjectGene Silencing
dc.subjectHumans
dc.subjectLactic Acid
dc.subjectLung
dc.subjectMagnetite Nanoparticles
dc.subjectParticle Size
dc.subjectPolyglycolic Acid
dc.subjectRNA, Small Interfering
dc.subjectTelomerase
dc.subjectTransfection
dc.titleGene silencing effect of SiRNA-magnetic modified with biodegradable copolymer nanoparticles on hTERT gene expression in lung cancer cell line.
dc.typearticle
dc.citation.volume44
dc.citation.issue1
dc.citation.spage188
dc.citation.epage93
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.3109/21691401.2014.934456


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