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Targeting efflux pumps to overcome antifungal drug resistance

期刊

FUTURE MEDICINAL CHEMISTRY
卷 8, 期 12, 页码 1485-1501

出版社

Newlands Press Ltd
DOI: 10.4155/fmc-2016-0050

关键词

ABC and MFS transporters; antifungal drug resistance; azole; chemosensitzation; heterologous expression; high-throughput screen

资金

  1. NIH [R01-DE016855-01, R03-MH087406-1A1, U54 MH074425/MH086490]
  2. Royal Society of New Zealand Marsden Fund [UOO1305]
  3. Health Research Council of New Zealand's International Investment Opportunities Fund [IIOF 09_04]
  4. Health Research Council of New Zealand
  5. University of Otago

向作者/读者索取更多资源

Resistance to antifungal drugs is an increasingly significant clinical problem. The most common antifungal resistance encountered is efflux pump-mediated resistance of Candida species to azole drugs. One approach to overcome this resistance is to inhibit the pumps and chemosensitize resistant strains to azole drugs. Drug discovery targeting fungal efflux pumps could thus result in the development of azole-enhancing combination therapy. Heterologous expression of fungal efflux pumps in Saccharomyces cerevisiae provides a versatile system for screening for pump inhibitors. Fungal efflux pumps transport a range of xenobiotics including fluorescent compounds. This enables the use of fluorescence-based detection, as well as growth inhibition assays, in screens to discover compounds targeting efflux-mediated antifungal drug resistance. A variety of medium-and high-throughput screens have been used to identify a number of chemical entities that inhibit fungal efflux pumps.

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