The Synergistic Effects of the Combination of Ciprofloxacin and Temozolomide on Human Glioblastoma A-172 Cell Line
Background: Combination therapy has generated remarkable motivation in the clinical setting since it boosts the therapeutic potential of anticancer drugs. Glioblastoma multiforme is the most common, aggressive malignant brain tumor which affects patients of all ages. This brain tumor is principal...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Shiraz University of Medical Sciences
2017-01-01
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Series: | Middle East Journal of Cancer |
Subjects: | |
Online Access: | http://mejc.sums.ac.ir/index.php/mejc/article/view/445/291 |
Summary: | Background: Combination therapy has generated remarkable motivation in the
clinical setting since it boosts the therapeutic potential of anticancer drugs. Glioblastoma
multiforme is the most common, aggressive malignant brain tumor which affects
patients of all ages. This brain tumor is principally resistant to treatment.
Methods: In this study, we combined temozolomide as a standard chemotherapeutic
drug for human glioblastoma multiforme, with ciprofloxacin in an attempt to
determine whether ciprofloxacin could potentiate the cytotoxic effects of temozolomide.
The glioblastoma A-172 cell line was exposed to ciprofloxacin and temozolomide either
alone or in combination for 24, 48 and 72 h. Cytotoxicity was measured by the MTT
assay.
Results: Ciprofloxacin and temozolomide induced tumor cell death in a dosedependent
manner with an IC50 value of 259.3 μM for ciprofloxacin and 62.5 μM for
temozolomide at 72 h. These values shifted to 22.8 μM for ciprofloxacin and 8.6 μM
for temozolomide in the presence of the IC50 of the other drug. The combination
index values were <1.
Conclusion: These results showed synergism across a broad range of concentrations
of ciprofloxacin and temozolomide in a glioblastoma tumor cell line. In this study,
ciprofloxacin increased the anti-tumor cytotoxic effects of temozolomide in the
glioblastoma A-172 cell line. |
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ISSN: | 2008-6709 2008-6687 |