Literature DB >> 16384725

Genotoxic potential of quinolone antimicrobials in the in vitro comet assay and micronucleus test.

Tadashi Itoh1, Kunitoshi Mitsumori, Satomi Kawaguchi, Yu F Sasaki.   

Abstract

The purpose of this study was to examine the genotoxicity of quinolone antimicrobials. We investigated the genotoxic potential of eight quinolones, namely nalidixic acid (NA), pipemidic acid (PPA), oxolinic acid (OA), piromidic acid (PA), enoxacin (ENX), ofloxacin (OFLX), norfloxacin (NFLX) and ciprofloxacin (CPFX), by the in vitro alkaline single-cell gel electrophoresis (comet) assay at pH>13. WTK-1 cells (mutant p53) were treated with each of the eight quinolones at 62.5-1000 microg/mL for 2, 4 and 20 h. NFLX and CPFX significantly induced DNA damage concentration-dependently after 4 and 20 h treatment, but this damage was recoverable. On the other hand, DNA was not damaged in the cells treated with six other quinolones. In the cells treated with NFLX and CPFX for 20 h, DNA migration was compared by the comet assay at pH 10, 12.1 and >13. The comet assay both at pH 12.1 and >13 showed increased DNA migration, but there was no positive response in the comet assay at pH 10. In the in vitro micronucleus (MN) test, WTK-1 cells were treated with each of four quinolones (NA, PPA, NFLX and CPFX) at 15.63-125 microg/mL for 20 h. NFLX significantly increased MNs in the cells, but no changes were noted in the cells treated with three other quinolones. These results suggest that NFLX and CPFX induced DNA single strand breaks (SSBs), and that NFLX-induced SSBs resulted in chromosome aberrations.

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Year:  2005        PMID: 16384725     DOI: 10.1016/j.mrgentox.2005.11.003

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  6 in total

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2.  Ciprofloxacin-induced G2 arrest and apoptosis in TK6 lymphoblastoid cells is not dependent on DNA double-strand break formation.

Authors:  Daniel J Smart; H Dorota Halicka; Frank Traganos; Zbigniew Darzynkiewicz; Gary M Williams
Journal:  Cancer Biol Ther       Date:  2007-10-08       Impact factor: 4.742

3.  Characterization of Abcc4 gene amplification in stepwise-selected mouse J774 macrophages resistant to the topoisomerase II inhibitor ciprofloxacin.

Authors:  Béatrice Marquez; Geneviève Ameye; Coralie M Vallet; Paul M Tulkens; Hélène A Poirel; Françoise Van Bambeke
Journal:  PLoS One       Date:  2011-12-05       Impact factor: 3.240

4.  High-content imaging analyses of γH2AX-foci and micronuclei in TK6 cells elucidated genotoxicity of chemicals and their clastogenic/aneugenic mode of action.

Authors:  Akira Takeiri; Kaori Matsuzaki; Shigeki Motoyama; Mariko Yano; Asako Harada; Chiaki Katoh; Kenji Tanaka; Masayuki Mishima
Journal:  Genes Environ       Date:  2019-02-05

Review 5.  The New Face of a Well-Known Antibiotic: A Review of the Anticancer Activity of Enoxacin and Its Derivatives.

Authors:  Karolina Jałbrzykowska; Alicja Chrzanowska; Piotr Roszkowski; Marta Struga
Journal:  Cancers (Basel)       Date:  2022-06-22       Impact factor: 6.575

6.  A small molecule drug promoting miRNA processing induces alternative splicing of MdmX transcript and rescues p53 activity in human cancer cells overexpressing MdmX protein.

Authors:  Georgios Valianatos; Barbora Valcikova; Katerina Growkova; Amandine Verlande; Jitka Mlcochova; Lenka Radova; Monika Stetkova; Michaela Vyhnakova; Ondrej Slaby; Stjepan Uldrijan
Journal:  PLoS One       Date:  2017-10-03       Impact factor: 3.240

  6 in total

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