脱氮酶
癌症研究
肝细胞癌
泛素
CTGF公司
基因敲除
化学
河马信号通路
日历年61
下调和上调
信号转导
生物
生物化学
基因
生长因子
受体
作者
Zelin Tian,Chen Xu,Weixiang He,Zhibin Lin,Wenjie Zhang,Kaishan Tao,Rui Ding,Xuan Zhang,Dou Ke-feng
出处
期刊:Cancer Letters
[Elsevier]
日期:2023-10-11
卷期号:577: 216439-216439
被引量:6
标识
DOI:10.1016/j.canlet.2023.216439
摘要
Hippo pathway plays a crucial role in the progression of hepatocellular carcinoma (HCC), and yes-associated protein (YAP) is one of the major factors of the Hippo pathway. However, the mechanism of abnormal YAP activation in HCC has not been well elucidated. Here, we screened a Deubiquitinating enzymes' (DUB) siRNA library targeting DUBs, and identified Ubiquitin Specific Peptidase 19 (USP19) as a specific deubiquitinating enzyme of YAP in HCC, which could stabilize YAP at K76 and K90 sites via removing the K48- and K11-linked ubiquitin chains. USP19 knockdown decreased the expression of YAP protein and its target gene (CTGF, CYR61, ANKRD1) expression. Through substantial in vivo and in vitro experiments, we prove that USP19 facilities the proliferation and migration of HCC. More importantly, we found that USP19 was upregulated in HCC tissues and associated with poor prognosis. In general, our research revealed a novel post-translational mechanism between USP19 and YAP in HCC, suggesting that USP19 may be a pivotal therapeutic target for HCC treatment.
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