细胞生长
癌症研究
化学
赖氨酸
肺癌
染色质
乙酰化
细胞培养
A549电池
细胞
组蛋白
癌症
细胞生物学
细胞模型
效力
癌细胞
癌
结构-活动关系
生物活性
细胞周期
肺
基因
染色质重塑
细胞毒性
下调和上调
药理学
信号转导
作者
Dymytrii Listunov,Alyssa Winkler,Joshua Ray,Brian M. Linhares,Bradley Clegg,Sidney Weaver,Eungi Kim,Sergei Zari,Se Ra Park,Sergey N Zolov,Sergei Chuikov,Liang Zhao,Yatrik M Shah,Venkateshwar G. Keshamouni,Jolanta Grembecka,Tomasz Cierpicki,Dymytrii Listunov,Alyssa Winkler,Joshua Ray,Brian M. Linhares
标识
DOI:10.1021/acs.jmedchem.5c02307
摘要
GAS41 is frequently overexpressed in Non-Small Cell Lung Cancer (NSCLC). GAS41 contains a YEATS domain, which recognizes acetylated lysine residues on histones to recruit protein complexes and facilitate transcription. Suppression of GAS41 in NSCLC models inhibits cellular proliferation and markedly reduces tumor growth in mouse xenografts, justifying the development of small-molecule inhibitors. We have employed structure-based design and medicinal chemistry optimization to discover DLG-41, a submicromolar inhibitor binding to the GAS41 YEATS domain. DLG-41 potently disrupts the association of GAS41 YEATS with chromatin in mammalian cells and inhibits the proliferation of NSCLC cell lines with submicromolar potency without significantly affecting normal lung fibroblasts. DLG-41 induces more effective growth inhibition in A549 versus GAS41-knockout cells, demonstrating on-target activity. DLG-41 treatment upregulates the CDKN1A gene and downregulates pathways associated with lung cancer cell identity, tumor migration, and invasion. DLG-41 is a promising chemical probe for targeting GAS41 protein in NSCLC models and has potential for future development.
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