Wakharde Archana Anandrao, Halbandge Shivkrupa Devrao, Phule Datta Baburao, Karuppayil Sankunny Mohan
School of Life Sciences (DST-FIST and UGC-SAP Sponsored) SRTM University (NAAC Accredited with "A" grade), Nanded, Maharashtra, India .
Assay Drug Dev Technol. 2018 Jul;16(5):232-246. doi: 10.1089/adt.2017.826. Epub 2018 Feb 15.
The human pathogen Candida albicans can grow as a biofilm on host tissues and on the surfaces of different prosthetic devices in a patient's body. Various studies have reported that biofilms formed by C. albicans are resistant to most of the currently used antibiotics including the widely prescribed drug, fluconazole. As such, novel strategies for the treatment of drug-resistant biofilms are required. Drug repositioning or the use of drugs outside their unique indication has the potential to radically change drug development. We have tested 16 anticancer drugs for their activities against C. albicans. For the first time, we are reporting repositioning of anticancer drugs as potential antibiofilm agents in C. albicans. Nine categories of drugs with different chemical modes of action effectively inhibited biofilms at a concentration range of 0.25-4 mg/mL, establishing their potential for the inhibition of biofilms. Human genes targeted by these drugs show significant identity with their homologous genes in C. albicans at the amino acid as well as nucleotide levels. This study indicates that anticancer drugs could be potential candidates for repositioning as anti-Candida biofilm agents.
人类病原体白色念珠菌可在宿主组织以及患者体内不同假体装置表面形成生物膜。多项研究报告称,白色念珠菌形成的生物膜对目前使用的大多数抗生素具有抗性,包括广泛使用的药物氟康唑。因此,需要新的策略来治疗耐药生物膜。药物重新定位或在其独特适应症之外使用药物有可能从根本上改变药物开发。我们测试了16种抗癌药物对白色念珠菌的活性。我们首次报告了将抗癌药物重新定位为白色念珠菌潜在的抗生物膜剂。九类具有不同化学作用模式的药物在0.25 - 4毫克/毫升的浓度范围内有效抑制生物膜,确立了它们抑制生物膜的潜力。这些药物靶向的人类基因在氨基酸和核苷酸水平上与其在白色念珠菌中的同源基因具有显著的一致性。这项研究表明,抗癌药物可能是重新定位为抗念珠菌生物膜剂的潜在候选药物。