Journal of the American Chemical Society · 2009 · 187 citations · 10 references
Life SciencesMedicinal ChemistryMolecular BiologyChromatin BiologyEpigeneticsMolecular OncologyChemical EpigeneticsEnzyme InhibitionHit-to-lead OptimizationAnticancer ActivityAntiproliferative AgentsAntiproliferative Drug ActionHistone Demethylase InhibitionHistone DemethylasesHistone DemethylationHistone-lysine MethylationLysine-targeted Inhibitors
Lysine specific demethylase 1 (LSD1) plays a key role in the regulation of gene expression by removing the methyl groups from methylated Lys4 of histone H3 (H3K4). Here we report the identification of the first small-molecule LSD1-selective inhibitors. These inhibitors show in vivo H3K4-methylating activity and antiproliferative activity and should be useful as lead structures for anticancer drugs and as tools for studying the biological roles of LSD1.
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Histone Demethylation Mediated by the Nuclear Amine Oxidase Homolog LSD1
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LSD1 demethylates repressive histone marks to promote androgen-receptor-dependent transcription
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