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Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC

Lung cancer is one of the most common tumors and its treatment is still inefficient. In our previous work we proved that ciprofloxacin has a different influence on five cancer cell lines. Here, we aimed to compare the biological effect of ciprofloxacin on cell lines representing different responses...

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Autores principales: KLOSKOWSKI, TOMASZ, GURTOWSKA, NATALIA, OLKOWSKA, JOANNA, NOWAK, JAKUB MARCIN, ADAMOWICZ, JAN, TWORKIEWICZ, JAKUB, DĘBSKI, ROBERT, GRZANKA, ALINA, DREWA, TOMASZ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583647/
https://www.ncbi.nlm.nih.gov/pubmed/23042104
http://dx.doi.org/10.3892/ijo.2012.1653
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author KLOSKOWSKI, TOMASZ
GURTOWSKA, NATALIA
OLKOWSKA, JOANNA
NOWAK, JAKUB MARCIN
ADAMOWICZ, JAN
TWORKIEWICZ, JAKUB
DĘBSKI, ROBERT
GRZANKA, ALINA
DREWA, TOMASZ
author_facet KLOSKOWSKI, TOMASZ
GURTOWSKA, NATALIA
OLKOWSKA, JOANNA
NOWAK, JAKUB MARCIN
ADAMOWICZ, JAN
TWORKIEWICZ, JAKUB
DĘBSKI, ROBERT
GRZANKA, ALINA
DREWA, TOMASZ
author_sort KLOSKOWSKI, TOMASZ
collection PubMed
description Lung cancer is one of the most common tumors and its treatment is still inefficient. In our previous work we proved that ciprofloxacin has a different influence on five cancer cell lines. Here, we aimed to compare the biological effect of ciprofloxacin on cell lines representing different responses after treatment, thus A549 was chosen as a sensitive model, C6 and B16 as highly resistant. Three different cell lines were analyzed (A549, B16 and C6). The characterization of continuous cell growth was analyzed with the Real-Time Cell Analyzer (RTCA)-DP system. Cytoskeletal changes were demonstrated using immunofluorescence. The cell cycle was analyzed using flow cytometry. Ciprofloxacin was cytostatic only against the A549 cell line. In the case of other tested cell lines a cytostatic effect was not observed. Cytoskeletal analysis confirms the results obtained with RTCA-DP. A549 cells were inhibited in the G2/M phase suggesting a mechanism related to topoisomerase II inhibition. The biological effects of ciprofloxacin support the hypothesis that this drug can serve as an adjuvant treatment for lung cancer, due to its properties enabling topoisomerase II inhibition.
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spelling pubmed-35836472013-03-04 Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC KLOSKOWSKI, TOMASZ GURTOWSKA, NATALIA OLKOWSKA, JOANNA NOWAK, JAKUB MARCIN ADAMOWICZ, JAN TWORKIEWICZ, JAKUB DĘBSKI, ROBERT GRZANKA, ALINA DREWA, TOMASZ Int J Oncol Articles Lung cancer is one of the most common tumors and its treatment is still inefficient. In our previous work we proved that ciprofloxacin has a different influence on five cancer cell lines. Here, we aimed to compare the biological effect of ciprofloxacin on cell lines representing different responses after treatment, thus A549 was chosen as a sensitive model, C6 and B16 as highly resistant. Three different cell lines were analyzed (A549, B16 and C6). The characterization of continuous cell growth was analyzed with the Real-Time Cell Analyzer (RTCA)-DP system. Cytoskeletal changes were demonstrated using immunofluorescence. The cell cycle was analyzed using flow cytometry. Ciprofloxacin was cytostatic only against the A549 cell line. In the case of other tested cell lines a cytostatic effect was not observed. Cytoskeletal analysis confirms the results obtained with RTCA-DP. A549 cells were inhibited in the G2/M phase suggesting a mechanism related to topoisomerase II inhibition. The biological effects of ciprofloxacin support the hypothesis that this drug can serve as an adjuvant treatment for lung cancer, due to its properties enabling topoisomerase II inhibition. D.A. Spandidos 2012-10-04 /pmc/articles/PMC3583647/ /pubmed/23042104 http://dx.doi.org/10.3892/ijo.2012.1653 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
KLOSKOWSKI, TOMASZ
GURTOWSKA, NATALIA
OLKOWSKA, JOANNA
NOWAK, JAKUB MARCIN
ADAMOWICZ, JAN
TWORKIEWICZ, JAKUB
DĘBSKI, ROBERT
GRZANKA, ALINA
DREWA, TOMASZ
Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC
title Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC
title_full Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC
title_fullStr Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC
title_full_unstemmed Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC
title_short Ciprofloxacin is a potential topoisomerase II inhibitor for the treatment of NSCLC
title_sort ciprofloxacin is a potential topoisomerase ii inhibitor for the treatment of nsclc
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583647/
https://www.ncbi.nlm.nih.gov/pubmed/23042104
http://dx.doi.org/10.3892/ijo.2012.1653
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