Kloskowski Tomasz, Fekner Zuzanna, Szeliski Kamil, Paradowska Michelle, Balcerczyk Daria, Rasmus Marta, Dąbrowski Paweł, Kaźmierski Łukasz, Drewa Tomasz, Pokrywczyńska Marta
Chair of Urology and Andrology, Department of Regenerative Medicine, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Chair of Urology and Andrology, Department of Tissue Engineering, Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
Front Oncol. 2023 Jul 18;13:1222411. doi: 10.3389/fonc.2023.1222411. eCollection 2023.
The anticancer properties of fluoroquinolones and the high concentrations they achieve in urine may help in bladder cancer therapy. This study aimed to analyze the properties of 4 fluoroquinolones as potential candidates for supportive treatment of bladder cancer.
Comparative analyses were performed on the cytotoxic effects of norfloxacin, enrofloxacin, moxifloxacin, and ofloxacin on normal and cancer urothelial cell lines. In 2D culture, the cytotoxic properties of fluoroquinolones were evaluated using MTT assay, real-time cell growth analysis, fluorescence and light microscopy, flow cytometry, and molecular analysis. In 3D culture, the properties of fluoroquinolones were tested using luminescence assays and confocal microscopy.
All tested fluoroquinolones in 2D culture decreased the viability of both tested cell lines in a dose- and timedependent manner. Lower concentrations did not influence cell morphology and cytoskeletal organization. In higher concentrations, destruction of the actin cytoskeleton and shrinkage of the nucleus was visible. Flow cytometry analysis showed cell cycle inhibition of bladder cancer cell lines in the G2/M phase. This influence was minimal in the case of normal urothelium cells. In both tested cell lines, increases in the number of late apoptotic cells were observed. Molecular analysis showed variable expression of studied genes depending on the drug and concentration. In 3D culture, tested drugs were effective only in the highest tested concentrations which was accompanied by caspase 3/7 activation and cytoskeleton degradation. This effect was hardly visible in non-cancer cell lines. According to the data, norfloxacin and enrofloxacin had the most promising properties. These two fluoroquinolones exhibited the highest cytotoxic properties against both tested cell lines. In the case of norfloxacin, almost all calculated LC values for bladder cancer cell lines were achievable in the urine. Enrofloxacin and norfloxacin can be used to support chemotherapy in bladder cancer patients.
氟喹诺酮类药物的抗癌特性以及它们在尿液中所能达到的高浓度可能有助于膀胱癌的治疗。本研究旨在分析4种氟喹诺酮类药物作为膀胱癌支持性治疗潜在候选药物的特性。
对诺氟沙星、恩诺沙星、莫西沙星和氧氟沙星对正常和癌性尿路上皮细胞系的细胞毒性作用进行了比较分析。在二维培养中,使用MTT法、实时细胞生长分析、荧光和光学显微镜、流式细胞术以及分子分析来评估氟喹诺酮类药物的细胞毒性特性。在三维培养中,使用发光测定法和共聚焦显微镜来测试氟喹诺酮类药物的特性。
在二维培养中,所有测试的氟喹诺酮类药物均以剂量和时间依赖性方式降低了两种测试细胞系的活力。较低浓度不会影响细胞形态和细胞骨架组织。在较高浓度下,可见肌动蛋白细胞骨架的破坏和细胞核的收缩。流式细胞术分析显示膀胱癌细胞系在G2/M期的细胞周期受到抑制。在正常尿路上皮细胞的情况下,这种影响最小。在两种测试细胞系中,均观察到晚期凋亡细胞数量增加。分子分析显示,根据药物和浓度的不同,所研究基因的表达存在差异。在三维培养中,测试药物仅在最高测试浓度下有效,同时伴有半胱天冬酶3/7激活和细胞骨架降解。这种效应在非癌细胞系中几乎不可见。根据数据,诺氟沙星和恩诺沙星具有最有前景的特性。这两种氟喹诺酮类药物对两种测试细胞系均表现出最高的细胞毒性特性。就诺氟沙星而言,膀胱癌细胞系几乎所有计算出的LC值在尿液中都能达到。恩诺沙星和诺氟沙星可用于支持膀胱癌患者的化疗。