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http://purl.uniprot.org/citations/27566175http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27566175http://www.w3.org/2000/01/rdf-schema#comment"Mammalian sterile 20-like kinase 1/2 (MST1/2) are core tumor suppressors in the Hippo signaling pathway. MST1/2 have been shown to regulate mitotic progression. Here, we report a novel mechanism for phospho-regulation of MST2 in mitosis and its biological significance in cancer. We found that the mitotic kinase cyclin-dependent kinase 1 (CDK1) phosphorylates MST2 in vitro and in vivo at serine 385 during antimitotic drug-induced G2/M phase arrest. This phosphorylation occurs transiently during unperturbed mitosis. Mitotic phosphorylation of MST2 does not affect its kinase activity or Hippo-YAP signaling. We further showed that mitotic phosphorylation-deficient mutant MST2-S385A possesses higher activity in suppressing cell proliferation and anchorage-independent growth in vitro and tumorigenesis in vivo. Together, our findings reveal a novel layer of regulation for MST2 in mitosis and its role in tumorigenesis."xsd:string
http://purl.uniprot.org/citations/27566175http://purl.org/dc/terms/identifier"doi:10.1016/j.cellsig.2016.08.013"xsd:string
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/author"Dong J."xsd:string
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/author"Chen X."xsd:string
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/author"Chen Y."xsd:string
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/name"Cell Signal"xsd:string
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/pages"1826-1832"xsd:string
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/title"MST2 phosphorylation at serine 385 in mitosis inhibits its tumor suppressing activity."xsd:string
http://purl.uniprot.org/citations/27566175http://purl.uniprot.org/core/volume"28"xsd:string
http://purl.uniprot.org/citations/27566175http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27566175
http://purl.uniprot.org/citations/27566175http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27566175
http://purl.uniprot.org/uniprot/#_A0A087WZ06-mappedCitation-27566175http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27566175
http://purl.uniprot.org/uniprot/#_A0A384MR07-mappedCitation-27566175http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27566175
http://purl.uniprot.org/uniprot/#_Q13188-mappedCitation-27566175http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27566175
http://purl.uniprot.org/uniprot/#_Q8NBU1-mappedCitation-27566175http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27566175
http://purl.uniprot.org/uniprot/A0A087WZ06http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27566175
http://purl.uniprot.org/uniprot/Q13188http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27566175
http://purl.uniprot.org/uniprot/Q8NBU1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27566175
http://purl.uniprot.org/uniprot/A0A384MR07http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/27566175