The utilization of poly(2-ethyl-2-oxazoline)-b-poly(epsilon-caprolactone) ellipsoidal particles for intracellular BIKDDA delivery to prostate cancer

dc.contributor.authorKocak, Polen
dc.contributor.authorOz, Umut Can
dc.contributor.authorBolat, Zeynep Büşra
dc.contributor.authorOzkose, Umut Ugur
dc.contributor.authorGulyuz, Sevgi
dc.contributor.authorTasdelen, Mehmet Atilla
dc.contributor.authorTelci, Dilek
dc.date.accessioned2020-12-20T06:49:36Z
dc.date.available2020-12-20T06:49:36Z
dc.date.issued2020
dc.departmentMühendislik ve Doğa Bilimleri Fakültesien_US
dc.descriptionWOS:000589603300001en_US
dc.description.abstractProstate cancer is the most common cancer, which is about 15-20% among male cancers worldwide. As most common strategies such as radiotherapy, chemotherapy, or surgery alone can be unsuccessful in the treatment of prostate cancer, this study aims to develop a new approach to deliver newly generated proapoptotic gene, BIKDDA, to androgen independent prostate cancer cells, 22RV1, using new generation nanocarriers called ellipsoids. As far as it is known, this is the first study that assesses the ability of proapoptotic gene BIKDDA to induce apoptosis in prostate cancer cell. BIKDDA encapsulating PEtOx-b-PCL-based ellipsoids are fabricated by solvent-switch method, and their morphology, size, and BIKDDA content are characterized. Gene delivery efficiency of BIKDDA loaded PEtOx-b-PCL ellipsoids is demonstrated by analysis of BIK mRNA expression with real-time PCR. The apoptotic effect of PEtOx-b-PCL ellipsoids loaded with BIKDDA (EPs-BIKDDA) on 22RV1 is shown by Annexin V staining. The obtained results demonstrate that the treatment of 22RV1 cells with EPs-BIKDDA can significantly increase BIK mRNA levels by 4.5-fold leading to cell death. This study not only represents BIKDDA as a potential therapeutic strategy in prostate cancer but also the capacity of ellipsoids as promising in vivo gene delivery vehicles.en_US
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [213M726]en_US
dc.description.sponsorshipP.K. and U.C.O. contributed equally to this work. The authors acknowledge that the financial support for this research was partially funded by the Scientific and Technological Research Council of Turkey (TUBITAK, Grant Number 213M726).en_US
dc.identifier.doi10.1002/mabi.202000287
dc.identifier.issn1616-5187
dc.identifier.issn1616-5195
dc.identifier.orcidZeynep Büşra Bolat |0000-0002-9216-6336
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1002/mabi.202000287
dc.identifier.urihttps://hdl.handle.net/20.500.12436/1750
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorBolat, Zeynep Büşra
dc.language.isoen
dc.publisherWiley-V C H Verlag Gmbhen_US
dc.relation.ispartofMacromolecular Bioscienceen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectellipsoidal particlesen_US
dc.subjectgene deliveryen_US
dc.subjectproapoptotic geneen_US
dc.subjectprostate canceren_US
dc.titleThe utilization of poly(2-ethyl-2-oxazoline)-b-poly(epsilon-caprolactone) ellipsoidal particles for intracellular BIKDDA delivery to prostate canceren_US
dc.typeArticle
dspace.entity.typePublication

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