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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2012
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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. |
format | Online Article Text |
id | pubmed-3583647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
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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