脱甲基酶
新生隐球菌
麦角甾醇
生物
抗真菌
微生物学
体内
体外
组蛋白
生物化学
基因
遗传学
作者
Tianyou Wang,Wanzhen Yang,Бо Лю,Yuanchao Wang,Yan Wang,Na Liu,Chunquan Sheng
标识
DOI:10.1021/acsinfecdis.2c00096
摘要
Invasive fungal infections are emerging as a global public health problem. The lack of effective antifungal drugs is the bottleneck of clinical antifungal treatment. To identify novel antifungal agents with new mechanisms of action, JIB-04, a Jumonji histone demethylase inhibitor, was identified to possess broad-spectrum antifungal activity by a cell-based screen. Particularly, JIB-04 effectively inhibited Jumonji demethylase activity and ergosterol biosynthesis of Cryptococcus neoformans cells, leading to in vitro and in vivo anti-Cryptococcus activity. It also significantly inhibited the virulence factors of C. neoformans including biofilm, melanin, capsule, and surface hydrophobicity. Thus, JIB-04 was validated as a potent antifungal agent for the treatment of cryptococcal meningitis and Jumonji histone demethylase was preliminarily identified as a potential target for the development of novel antifungal therapeutics.
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