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http://purl.uniprot.org/citations/26183061http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26183061http://www.w3.org/2000/01/rdf-schema#comment"The activity of the phosphatase and tensin homologue (PTEN) is known to be suppressed via post-translational modification. However, the mechanism and physiological significance by which post-translational modifications lead to PTEN suppression remain unclear. Here we demonstrate that PTEN destabilization is induced by EGFR- or oncogenic PI3K mutation-mediated AKT activation in cervical cancer. EGFR/PI3K/AKT-mediated ubiquitination and degradation of PTEN are dependent on the MKRN1 E3 ligase. These processes require the stabilization of MKRN1 via AKT-mediated phosphorylation. In cervical cancer patients with high levels of pAKT and MKRN1 expression, PTEN protein levels are low and correlate with a low 5-year survival rate. Taken together, our results demonstrate that PI3K/AKT signals enforce positive-feedback regulation by suppressing PTEN function."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.org/dc/terms/identifier"doi:10.1038/ncomms8769"xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Kim J.H."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Lee M.S."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Ko A."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Lee C."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Lee H.W."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Song J."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Chun K.H."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Cho H."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Han H.J."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Chung J.Y."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Hewitt S.M."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/author"Jeong M.H."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/name"Nat Commun"xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/pages"7769"xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/title"PI3K/AKT activation induces PTEN ubiquitination and destabilization accelerating tumourigenesis."xsd:string
http://purl.uniprot.org/citations/26183061http://purl.uniprot.org/core/volume"6"xsd:string
http://purl.uniprot.org/citations/26183061http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26183061
http://purl.uniprot.org/citations/26183061http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26183061
http://purl.uniprot.org/uniprot/#_Q15008-mappedCitation-26183061http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26183061
http://purl.uniprot.org/uniprot/#_A1L0W6-mappedCitation-26183061http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26183061
http://purl.uniprot.org/uniprot/#_B4DM96-mappedCitation-26183061http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26183061