Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/4180
Title: Cisplatin cytotoxicity is enhanced with zoledronic acid in A549 lung cancer cell line: Preliminary results of an in vitro study
Authors: Ozturk, O.H.
Bozcuk, H.
Burgucu, D.
Ekinci, D.
Ozdogan, M.
Akca, S.
Yıldız, Mustafa
Keywords: Apoptosis
Cisplatin
Gemcitabin
Lung cancer
Zoledronic acid
3 (4,5 dimethyl 2 thiazolyl) 2,5 diphenyltetrazolium bromide
bisphosphonic acid derivative
cisplatin
fluorescein isothiocyanate
gemcitabine
lipocortin 5
zoledronic acid
apoptosis
article
cancer cell culture
cell strain A549
controlled study
drug cytotoxicity
drug mechanism
drug potentiation
human
human cell
in vitro study
lung cancer
Antineoplastic Agents
Bone Density Conservation Agents
Cell Death
Cell Line, Tumor
Cell Proliferation
Deoxycytidine
Diphosphonates
Drug Screening Assays, Antitumor
Drug Synergism
Humans
Imidazoles
Lung Neoplasms
Abstract: We tested whether zoledronic acid, a biphosphonate with proposed apoptotic activity, augmented the cytotoxicity of cisplatin and/or gemcitabine in A549 lung cancer cell line. This cell line was subjected to different concentrations of the above chemotherapeutic agents and zoledronic acid. Cytotoxicity was assessed by the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrasodium bromide) assay. Particularly, zoledronic acid in 100 micromolar (µM) concentration augmented the cytotoxicity by cisplatin 1 µg/ml from 25% to 70% (Z = 3.22, P = 0.0072). A significant portion of cells underwent apoptosis with or without zoledronic acid, but more so with the combination treatment as assessed by an Annexin V-FITC apoptosis detection kit. However, 100 µM zoledronic acid showed 50% cytotoxicity on its own, but failed to improve cytotoxicity by Gemcitabine. Thus, we show for the first time in a lung cancer cell line that zoledronic acid bears cytotoxic potential on its own and in conjunction with cisplatin. The clinical potential of this finding should be further studied. © 2007 International Federation for Cell Biology.
URI: https://hdl.handle.net/11499/4180
https://doi.org/10.1016/j.cellbi.2007.02.004
ISSN: 1065-6995
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

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