可药性
生物
泛素
泛素连接酶
细胞生物学
癌症研究
非整倍体
泛素蛋白连接酶类
遗传学
基因
计算生物学
染色体
作者
Nektaria Maria Leli,Constantinos Koumenis
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2023-03-01
卷期号:13 (3): 535-537
被引量:3
标识
DOI:10.1158/2159-8290.cd-22-1440
摘要
Tumor fitness coessentiality gene analysis that aims to expand the repertoire of druggable targets reveals a novel ubiquitin ligase complex, the BICR6 module. Along with the other complex members (UBA6, KCMF1, and UBR4), BIRC6 selectively contributes to the survival of a subset of epithelial tumors with a high degree of aneuploidy by ubiquitinating and suppressing HRI, a component of the integrated stress response adaptive pathway. See related article by Cervia et al., p. 766 (2).
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