
pmid: 20211752
Ciprofloxacin is an antibiotic that belongs to fluoroquinoles, characterized by broad spectrum of action against pathogens, especially Gram(-) aerobic bacilli. For a long time, it has been thought that ciprofloxacin has an effect only on bacterial cells. Now it is known, that this drug can significantly affect eukaryotic cells including human cancer cells. Its bactericidal action relay on inhibition of topoisomerase II, enzyme responsible for alterations in 3D structure of DNA during replication, transcription and chromatin condensation. Thanks to that, ciprofloxacin can induce cell cycle arrest and apoptosis of cancer cells. The effectiveness of ciprofloxacin was confirmed in several in vitro studies on tumor cell lines such as: human bladder cells, leukaemic cell lines, human osteosarcoma cells, human prostate cancer cells, human colorectal carcinoma cells and human non-small cell lung cancer cell line. Ciprofloxacin is particularly effective against non-small cell lung cancer mainly due to accumulation of ciprofloxacin in lung tissue after intravenous administration and its toxicity against lung cancer lines in vitro in a concentration and time-dependent manner.
Lung Neoplasms, Dose-Response Relationship, Drug, Cell Cycle, Antineoplastic Agents, Apoptosis, Ciprofloxacin, Carcinoma, Non-Small-Cell Lung, Cell Line, Tumor, Humans, Topoisomerase II Inhibitors, Fluoroquinolones
Lung Neoplasms, Dose-Response Relationship, Drug, Cell Cycle, Antineoplastic Agents, Apoptosis, Ciprofloxacin, Carcinoma, Non-Small-Cell Lung, Cell Line, Tumor, Humans, Topoisomerase II Inhibitors, Fluoroquinolones
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