Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14365/1020
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dc.contributor.authorAkinoglu, E. M.-
dc.contributor.authorOzbilgin, K.-
dc.contributor.authorSonmez, P. Kilicaslan-
dc.contributor.authorOzkut, M. M.-
dc.contributor.authorGiersig, M.-
dc.contributor.authorInan, S.-
dc.contributor.authorGumustepe, E.-
dc.date.accessioned2023-06-16T12:58:48Z-
dc.date.available2023-06-16T12:58:48Z-
dc.date.issued2017-
dc.identifier.issn2194-0509-
dc.identifier.issn2194-0517-
dc.identifier.urihttps://doi.org/10.1007/s40204-017-0078-6-
dc.identifier.urihttps://hdl.handle.net/20.500.14365/1020-
dc.description.abstractThe aim of the current study was to determine whether the MWCNT-based scaffold has a suitable structure for cell growth and provides a biocompatible environment for human MDA-MB-231 cell lines. MWCNT-based nanostructured scaffolds were produced by plasma-enhanced chemical vapor deposition (PECVD) technique. MDA-MB-231 cells were seeded on MWCNTs-textured silicon scaffolds and on pristine silicon surfaces. After 1 week of culturing, the scaffolds were prepared for SEM analysis and immunocytochemical staining was performed for the two groups (MWCNT scaffold and pristine silicon surface), using MMP-2, MMP-9, PI3K, AKT and NF-kappa B primary antibodies. SEM analyses showed that the MDA-MB-231 cells better adhered to the MWCNT-based nanostructured scaffold than the pristine silicon surface. Immunohistochemical activity of the MDA-MB-231 cells on both materials has similar staining with anti-AKT MMP-2, MMP-9 and NF-kappa B primary antibodies. Therefore, the results of the present study suggest that the MWCNT-based scaffolds enhanced cell adhesion to the scaffold and exhibited more biomimetic properties and physiological adaptation with the potential to be used for in vitro metastasis studies of BrCa cell lines.en_US
dc.description.sponsorshipGuangdong Innovative and Entrepreneurial Team Program Plasmonic Nanomaterials and Quantum Dots for Light Management in Optoelectronic Devices [2016ZT06C517]en_US
dc.description.sponsorshipThe authors thank Klaus Ellmer and Daniel Abou-Ras from HZB for laboratory access, and Karsten Harbauer for technical help. The work was funded by the Guangdong Innovative and Entrepreneurial Team Program Plasmonic Nanomaterials and Quantum Dots for Light Management in Optoelectronic Devices (No. 2016ZT06C517).en_US
dc.language.isoenen_US
dc.publisherSpringer Heidelbergen_US
dc.relation.ispartofProgress in Bıomaterıalsen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectMDA-MB-231en_US
dc.subjectBreast canceren_US
dc.subjectMWCNTsen_US
dc.subjectBiocompatibilityen_US
dc.subjectImmunohistochemistryen_US
dc.subjectMatrix Metalloproteinases Mmp-2en_US
dc.subjectMek Inhibitoren_US
dc.subjectIn-Vivoen_US
dc.subjectMetastasisen_US
dc.subjectTissueen_US
dc.subjectProgressionen_US
dc.subjectPi3ken_US
dc.titleBiocompatibility of vertically aligned multi-walled carbon nanotube scaffolds for human breast cancer cell line MDA-MB-231en_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s40204-017-0078-6-
dc.identifier.pmid29147947en_US
dc.departmentİzmir Ekonomi Üniversitesien_US
dc.authoridGumustepe, Esra/0000-0002-3664-4663-
dc.authoridAkinoglu, Eser/0000-0002-0463-5543-
dc.authoridÖzkut, Mahmud Mustafa/0000-0001-8725-8909-
dc.authoridGiersig, Michael/0000-0002-5394-0413-
dc.authorwosidGumustepe, Esra/ABG-4125-2020-
dc.authorwosidAkinoglu, Eser/GQO-8875-2022-
dc.authorwosidÖzkut, Mahmud Mustafa/A-5027-2019-
dc.identifier.volume6en_US
dc.identifier.issue4en_US
dc.identifier.startpage189en_US
dc.identifier.endpage196en_US
dc.identifier.wosWOS:000416724000006en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopusqualityQ1-
dc.identifier.wosqualityQ2-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.languageiso639-1en-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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