Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC
Author(s) -
Tomasz Kloskowski,
Natalia Gurtowska,
Joanna Olkowska,
Jakub Marcin Nowak,
Jan Adamowicz,
J. Tworkiewicz,
Robert Dębski,
Alina Grzanka,
Tomasz Drewa
Publication year - 2012
Publication title -
international journal of oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.405
H-Index - 122
ISSN - 1019-6439
DOI - 10.3892/ijo.2012.1653
Subject(s) - cell cycle , topoisomerase , a549 cell , cell culture , biology , flow cytometry , cell , cancer research , cell growth , apoptosis , lung cancer , microbiology and biotechnology , oncology , medicine , biochemistry , in vitro , genetics
Lung cancer is one of the most common tumors and its treatment is stillinefficient. In our previous work we proved that ciprofloxacin has a differentinfluence on five cancer cell lines. Here, we aimed to compare the biologicaleffect of ciprofloxacin on cell lines representing different responses after treatment,thus A549 was chosen as a sensitive model, C6 and B16 as highly resistant. Threedifferent cell lines were analyzed (A549, B16 and C6). The characterization ofcontinuous cell growth was analyzed with the Real-Time Cell Analyzer (RTCA)-DPsystem. Cytoskeletal changes were demonstrated using immunofluorescence. The cellcycle was analyzed using flow cytometry. Ciprofloxacin was cytostatic only againstthe A549 cell line. In the case of other tested cell lines a cytostatic effectwas not observed. Cytoskeletal analysis confirms the results obtained with RTCA-DP.A549 cells were inhibited in the G2/M phase suggesting a mechanism related totopoisomerase II inhibition. The biological effects of ciprofloxacin support thehypothesis that this drug can serve as an adjuvant treatment for lung cancer,due to its properties enabling topoisomerase II inhibition.
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