Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4646
Full metadata record
DC FieldValueLanguage
dc.contributor.authorYıldız, Mustafa-
dc.contributor.authorCelik-Ozenci, C.-
dc.contributor.authorAkan, S.-
dc.contributor.authorAkan, I.-
dc.contributor.authorSati, L.-
dc.contributor.authorDemir, R.-
dc.contributor.authorSavas, B.-
dc.date.accessioned2019-08-16T11:35:52Z
dc.date.available2019-08-16T11:35:52Z
dc.date.issued2006-
dc.identifier.issn1065-6995-
dc.identifier.urihttps://hdl.handle.net/11499/4646-
dc.identifier.urihttps://doi.org/10.1016/j.cellbi.2005.11.008-
dc.description.abstractWe have explored the action of zoledronic acid, which has an apoptotic effect and is used as an agent for treating skeletal metastases and osteoporosis, in the presence of vinblastine, and whether this effect is associated with MRP-1 (multidrug resistance protein-1) expression. HEK (human embryonic kidney) 293 cells were transfected to form the multidrug resistant cell line designated 293MRP (MRP-1 expressing HEK293 cells). Both lines were treated with varying concentrations of vinblastine and zoledronic acid. Apoptosis was determined by the TUNEL (deoxyuridine triphosphate nick end-labeling) method. The type of treatment, MRP-1 expression status, and the type of treatment with respect to MRP-1 expression status significantly affected (P < 0.001) the degree of apoptosis. The largest increase in cytotoxicity was noted in HEK293 cells, when 100 µmol zoledronic acid was added to 4 µg/ml vinblastine (an increment of 80.3%, P < 0.001). This preliminary work shows that zoledronic acid acts synergistically with vinblastine to induce apoptosis in an MRP-1 dependent way. © 2005 Published by Elsevier Ltd on behalf of International Federation for Cell Biology.en_US
dc.language.isoenen_US
dc.relation.ispartofCell Biology Internationalen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectApoptosisen_US
dc.subjectMultidrug resistanceen_US
dc.subjectTUNELen_US
dc.subjectVinblastineen_US
dc.subjectZoledronic aciden_US
dc.subjectmultidrug resistance protein 1en_US
dc.subjectvinblastineen_US
dc.subjectzoledronic aciden_US
dc.subjectapoptosisen_US
dc.subjectarticleen_US
dc.subjectcytotoxicityen_US
dc.subjectdose responseen_US
dc.subjectdrug combinationen_US
dc.subjectdrug inhibitionen_US
dc.subjectdrug mechanismen_US
dc.subjectdrug potentiationen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectin vitro studyen_US
dc.subjectnick end labelingen_US
dc.subjectDiphosphonatesen_US
dc.subjectDrug Synergismen_US
dc.subjectHumansen_US
dc.subjectImidazolesen_US
dc.subjectImmunoblottingen_US
dc.subjectP-Glycoproteinen_US
dc.titleZoledronic acid is synergic with vinblastine to induce apoptosis in a multidrug resistance protein-1 dependent way: An in vitro studyen_US
dc.typeArticleen_US
dc.identifier.volume30en_US
dc.identifier.issue3en_US
dc.identifier.startpage278
dc.identifier.startpage278en_US
dc.identifier.endpage282en_US
dc.identifier.doi10.1016/j.cellbi.2005.11.008-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid16458542en_US
dc.identifier.scopus2-s2.0-33244478118en_US
dc.identifier.wosWOS:000236092700013en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale_University-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Show simple item record



CORE Recommender

SCOPUSTM   
Citations

9
checked on Nov 16, 2024

WEB OF SCIENCETM
Citations

9
checked on Nov 16, 2024

Page view(s)

30
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.