Division of Urology, Rinku General Medical Center, Izumisano Municipal Hospital, Izumisano City, Osaka, Japan.
Urology. 2009 Dec;74(6):1370-6. doi: 10.1016/j.urology.2009.03.006. Epub 2009 May 9.
To study the antitumor effects of fleroxacin against bladder tumor cell lines and the synergistic effect with 5-fluorouracil (5-FU) both in vitro and in vivo.
In vitro, the MBT-2 and T-24 urothelial carcinoma cell lines were exposed to fleroxacin in concentrations of 0-800 microg/mL for 12, 24, and 48 hours. Cytotoxicity was evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide colorimetric assay. Synergism of fleroxacin with 5-FU was evaluated using the normalized isobologram and combination index by CalcuSyn for Windows computer program. In vivo, 4-week-old female C57BL/6 mice were orally administered fleroxacin and/or 5-FU 1 week before starting administration of a carcinogenic agent (0.05% N-butyl-N-(4-hydroxybutyl)nitrosamine) for 12 weeks. The mice were killed 8 weeks after the end of administration for histologic evaluation of the urinary bladder.
Fleroxacin significantly inhibited cell proliferation in a dose- and time-dependent manner at concentrations of 50-800 microg/mL for 12, 24, and 48 hours. The inhibitory effects of fleroxacin combined with 5-FU appeared synergistic using normalized isobologram and combination index analysis. In vivo, no significant changes in bladder tumor frequency were noted between the control and fleroxacin and 5-FU groups. Significant inhibition of tumor frequency was observed only when fleroxacin was administered with 5-FU.
Fleroxacin combined with 5-FU inhibited the proliferation of bladder tumor cell lines both in vitro and in vivo. This combination therapy might be applicable in clinical settings.
研究氟罗沙星对膀胱肿瘤细胞系的抗肿瘤作用,以及氟罗沙星与 5-氟尿嘧啶(5-FU)联合应用的体内外协同作用。
体外实验中,将 MBT-2 和 T-24 尿路上皮癌细胞系暴露于 0-800μg/ml 的氟罗沙星中 12、24 和 48 小时。采用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐比色法评估细胞毒性。采用归一化等效应线和 Windows 计算机程序 CalcuSyn 的组合指数评估氟罗沙星与 5-FU 的协同作用。体内实验中,4 周龄雌性 C57BL/6 小鼠在开始给予致癌剂(0.05% N-丁基-N-(4-羟丁基)亚硝胺)前 1 周,口服给予氟罗沙星和/或 5-FU,连续给药 12 周。给药结束后 8 周处死小鼠,对膀胱进行组织学评估。
氟罗沙星在 50-800μg/ml 的浓度下,在 12、24 和 48 小时的时间内,以剂量和时间依赖的方式显著抑制细胞增殖。采用归一化等效应线和组合指数分析,氟罗沙星联合 5-FU 的抑制作用呈协同作用。体内实验中,与对照组和氟罗沙星组及 5-FU 组相比,膀胱肿瘤频率无显著变化。仅当氟罗沙星与 5-FU 联合应用时,才能观察到肿瘤频率的显著抑制。
氟罗沙星联合 5-FU 可抑制膀胱肿瘤细胞系的体外和体内增殖。这种联合治疗方法可能适用于临床应用。