The deubiquitinating enzyme USP19 facilitates hepatocellular carcinoma progression through stabilizing YAP

被引:9
|
作者
Tian, Zelin [1 ]
Xu, Chen [1 ]
He, Weixiang [2 ]
Lin, Zhibin [1 ]
Zhang, Wenjie [1 ,3 ]
Tao, Kaishan [1 ]
Ding, Rui [1 ]
Zhang, Xuan [1 ]
Dou, Kefeng [1 ]
机构
[1] Air Force Med Univ, Xijing Hosp, Dept Hepatobiliary Surg, Xian, Peoples R China
[2] Air Force Med Univ, Xijing Hosp, Dept Urol, Xian, Peoples R China
[3] Northwest Univ, Chinese Educ Minist, Key Lab Western Resources & Modern Biotechnol, Coll Life Sci,Key Lab Biotechnol Shaanxi Prov, Xian, Peoples R China
关键词
USP19; Deubiquitination; Hippo pathway; HCC; HIPPO PATHWAY; TUMORIGENESIS; AUTOPHAGY; CANCER;
D O I
10.1016/j.canlet.2023.216439
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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.
引用
收藏
页数:12
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