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http://purl.uniprot.org/citations/29550816http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/29550816http://www.w3.org/2000/01/rdf-schema#comment"BACKGROUND/AIMS:An increasing number of studies have linked erythropoietin-producing hepatocellular carcinoma (Eph) family receptor tyrosine kinases to cancer progression. However, little knowledge is available about the regulation of their functions in cancer. METHODS:SUMOylation was analyzed by performing Ni2+-NTA pull-down assay and immunoprecipitation. Cell proliferation, anchorage-independent growth, and tumorigenesis in vivo were examined by cell counting kit-8, soft agar colony formation assay, and a xenograft tumor mouse model, respectively. RESULTS:We found that EphB1 was post-translationally modified by the small ubiquitin-like modifier (SUMO) protein at lysine residue 785. Analysis of wild-type EphB1 and SUMOylation-deficient EphB1 K785R mutant revealed that SUMOylation of EphB1 suppressed cell proliferation, anchorage-independent cell growth, and xenograft tumor growth. Mechanistic study showed that SUMOylation of EphB1 repressed activation of its downstream signaling molecule PKCγ, and consequently inhibited tumorigenesis. A reciprocal regulatory loop between PKCγ and SUMOylation of EphB1 was also characterized. CONCLUSION:Our findings identify SUMO1 as a novel key regulator of EphB1-mediated tumorigenesis."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.org/dc/terms/identifier"doi:10.1159/000488174"xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Chen R."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Chen Q."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Jin H."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Huang J."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Deng R."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Wang Y."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Zhang H."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Yu J."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Zhao X."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Yuan H."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/author"Dou J."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/name"Cell Physiol Biochem"xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/pages"2283-2292"xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/title"Sumoylation of EphB1 Suppresses Neuroblastoma Tumorigenesis via Inhibiting PKCgamma Activation."xsd:string
http://purl.uniprot.org/citations/29550816http://purl.uniprot.org/core/volume"45"xsd:string
http://purl.uniprot.org/citations/29550816http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/29550816
http://purl.uniprot.org/citations/29550816http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/29550816
http://purl.uniprot.org/uniprot/#_B2R5T1-mappedCitation-29550816http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29550816
http://purl.uniprot.org/uniprot/#_A0A804HIU5-mappedCitation-29550816http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29550816
http://purl.uniprot.org/uniprot/#_B7Z3V9-mappedCitation-29550816http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29550816
http://purl.uniprot.org/uniprot/#_B7Z3W6-mappedCitation-29550816http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29550816