RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/34339800http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34339800http://www.w3.org/2000/01/rdf-schema#comment"Dysregulated ubiquitination of tumor-related proteins plays a critical role in tumor development and progression. The deubiquitinase USP22 is aberrantly expressed in certain types of cancer and contributes to aggressive tumor progression. However, the precise mechanism underlying the pro-tumorigenic function of USP22 in hepatocellular carcinoma (HCC) remains unclear. Here, we report that E2F6, a pocket protein-independent transcription repressor, is essential for HCC cell growth, and that its activities are controlled by USP22-mediated deubiquitination. USP22 interacts with and stabilizes E2F6, resulting in the transcriptional repression of phosphatase DUSP1. Moreover, the process involving DUSP1 repression by E2F6 strengthens AKT activation in HCC cells. Therefore, these findings provide mechanistic insights into the USP22-mediated control of oncogenic AKT signaling, emphasizing the importance of USP22-E2F6 regulation in HCC development."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.org/dc/terms/identifier"doi:10.1016/j.canlet.2021.07.044"xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Chen Z."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Liu Y."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Liu Y.'"xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Yang Z."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Zhang L."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Xu X."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Wang B."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Xu G."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Xiang L."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Jing T."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/author"Jiao K."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/name"Cancer Lett"xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/pages"266-277"xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/title"Deubiquitination of the repressor E2F6 by USP22 facilitates AKT activation and tumor growth in hepatocellular carcinoma."xsd:string
http://purl.uniprot.org/citations/34339800http://purl.uniprot.org/core/volume"518"xsd:string
http://purl.uniprot.org/citations/34339800http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/34339800
http://purl.uniprot.org/citations/34339800http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/34339800
http://purl.uniprot.org/uniprot/#_Q9UPT9-mappedCitation-34339800http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34339800
http://purl.uniprot.org/uniprot/Q9UPT9http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/34339800