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Anticancer drugs as enhancers of fluconazole sensitivity in Candida albicans

机译:抗癌药可增强白色念珠菌对氟康唑的敏感性

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Prescribing fluconazole for prophylaxis and treatment of?Candida albicans?infections in cancer patients is a common practice. The rational of using anti-?Candida?drugs along with cancer drugs is debating, because of contradictory results showing either increase or decrease in antifungal sensitivity. In an effort to analyse this, effect of short term exposure to thirty anticancer agents on minimum inhibitory concentration (MIC) of fluconazole was studied in a micro plate based assay. Antitumor antibiotic, 5- flurouracil was the most effective sensitizer of?C. albicans, causing sixty-four fold increase in fluconazole susceptibility. Eight of the selected anticancer molecules had potential to lower fluconazole MIC by sixteen fold, so that it comes down to 0.062 μg/ml. Three of the cancer drugs caused eight fold increase in the antifungal sensitivity. Effective molecules belonged to six different classes, indicating that ability to sensitize?C. albicans?towards fluconazole was not confined to a specific group. Our?in vitro?study, for the first time reveals efficacy of the thirty anticancer drugs to act as sensitizers in?C. albicans.
机译:开处方氟康唑预防和治疗癌症患者的白色念珠菌感染是一种常见的做法。由于抗真菌敏感性增加或降低的矛盾结果,抗癌药物与抗癌药物一起使用的合理性正在争论。为了对此进行分析,在基于微孔板的测定中研究了短期暴露于三十种抗癌剂对氟康唑的最低抑菌浓度(MIC)的影响。抗肿瘤抗生素5-氟尿嘧啶是?C最有效的敏化剂。白色念珠菌,引起氟康唑敏感性增加六十四倍。所选的八种抗癌分子具有将氟康唑MIC降低16倍的潜力,因此可降至0.062μg/ ml。三种抗癌药引起的抗真菌敏感性增加了八倍。有效分子属于六个不同的类别,表明具有敏化ΔC的能力。白色念珠菌对氟康唑的使用不限于特定人群。我们的体外研究首次揭示了三十种抗癌药在体内用作敏化剂的功效。白色的。

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