High-throughput screening to identify inhibitors of lysine demethylases

被引:1
作者
Gale, Molly [1 ]
Yan, Qin [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
关键词
high-throughput screening; JmjC; KDM; LSD1; lysine demethylase; small-molecule inhibitor; RAPIDFIRE MASS-SPECTROMETRY; NF-KAPPA-B; HISTONE DEMETHYLASES; LSD1; INHIBITORS; TR-FRET; ASSAYS; IDENTIFICATION; METHYLATION; CANCER; TARGETS;
D O I
10.2217/EPI.14.63
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Lysine demethylases (KDMs) are epigenetic regulators whose dysfunction is implicated in the pathology of many human diseases including various types of cancer, inflammation and X-linked intellectual disability. Particular demethylases have been identified as promising therapeutic targets, and tremendous efforts are being devoted toward developing suitable small-molecule inhibitors for clinical and research use. Several high-throughput screening strategies have been developed to screen for small-molecule inhibitors of KDMs, each with advantages and disadvantages in terms of time, cost, effort, reliability and sensitivity. In this Special Report, we review and evaluate the high-throughput screening methods utilized for discovery of novel small-molecule KDM inhibitors.
引用
收藏
页码:57 / 65
页数:9
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