USP24 promotes hepatocellular carcinoma progression by deubiquitinating and stabilizing YAP1

Yes-associated protein 1 (YAP1) plays a pivotal role in promoting the progression of hepatocellular carcinoma (HCC). Emerging evidence shows that inducing YAP1 degradation represents a promising strategy. Here, we identified USP24 as a bona fide deubiquitinating enzyme for YAP1. USP24 directly interacts with and deubiquitinates YAP1, thereby stabilizing YAP1 protein levels. Clinically, USP24 was significantly upregulated in HCC tissues and correlated with poor patient prognosis. Depletion of USP24 significantly suppressed the proliferation of HCC cells in vitro, which could be rescued by restoration of YAP1. Consistent with these findings, USP24 knockdown inhibited tumor growth in a xenograft mouse model. Overall, our study reveals that the USP24/YAP1 axis plays a critical role in the malignant progression of HCC, thus providing rationale for potential therapeutic interventions for YAP1-driven HCC.

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Publication Details

Journal
Cancer Cell International
Published
2025-04-26
DOI
https://doi.org/10.1186/s12935-025-03796-w
Citations
4
Primary Topic
Hippo pathway signaling and YAP/TAZ
Type
article
Field-Weighted Citation Impact
4.61

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article

USP24 promotes hepatocellular carcinoma progression by deubiquitinating and stabilizing YAP1

Yanfei Luo, Huizhuang Shan, Lei Zhang, Lei Xian et al.
4 citations
Cancer Cell International
Hippo pathway signaling and YAP/TAZ
4.61
article

USP24 promotes hepatocellular carcinoma progression by deubiquitinating and stabilizing YAP1

Yanfei Luo, Huizhuang Shan, Lei Zhang, Lei Xian, Yingli Wu, Yanfen Ge, Wenmin Li, Junru Liu, Xinhua Xiao, Ting Lin, M. D. Lan, Jiaguo Yuan
article en
4 citations

Abstract

Yes-associated protein 1 (YAP1) plays a pivotal role in promoting the progression of hepatocellular carcinoma (HCC). Emerging evidence shows that inducing YAP1 degradation represents a promising strategy. Here, we identified USP24 as a bona fide deubiquitinating enzyme for YAP1. USP24 directly interacts with and deubiquitinates YAP1, thereby stabilizing YAP1 protein levels. Clinically, USP24 was significantly upregulated in HCC tissues and correlated with poor patient prognosis. Depletion of USP24 significantly suppressed the proliferation of HCC cells in vitro, which could be rescued by restoration of YAP1. Consistent with these findings, USP24 knockdown inhibited tumor growth in a xenograft mouse model. Overall, our study reveals that the USP24/YAP1 axis plays a critical role in the malignant progression of HCC, thus providing rationale for potential therapeutic interventions for YAP1-driven HCC.

Cancer Cell InternationalVol. 25(1)
Guangdong Academy of Medical Sciences (CN), Guangdong Provincial People's Hospital (CN), Southern Medical University (CN), Guangzhou Medical University (CN)
National Natural Science Foundation of China, Basic and Applied Basic Research Foundation of Guangdong Province
Openalex Percentile: Top 6%
Hippo pathway signaling and YAP/TAZ
4.61
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