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http://purl.uniprot.org/citations/31697807http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31697807http://www.w3.org/2000/01/rdf-schema#comment"Altered metabolism fuels 2 hallmark properties of cancer cells: unlimited proliferation and differentiation blockade. Adenosine monophosphate-activated protein kinase (AMPK) is a master regulator of bioenergetics crucial for glucose metabolism in acute myeloid leukemia (AML), and its inhibition delays leukemogenesis, but whether the metabolic function of AMPK alters the AML epigenome remains unknown. Here, we demonstrate that AMPK maintains the epigenome of MLL-rearranged AML by linking acetyl-coenzyme A (CoA) homeostasis to Bromodomain and Extra-Terminal domain (BET) protein recruitment to chromatin. AMPK deletion reduced acetyl-CoA and histone acetylation, displacing BET proteins from chromatin in leukemia-initiating cells. In both mouse and patient-derived xenograft AML models, treating with AMPK and BET inhibitors synergistically suppressed AML. Our results provide a therapeutic rationale to target AMPK and BET for AML therapy."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.org/dc/terms/identifier"doi:10.1182/blood.2019001076"xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Jiang Y."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Lin C.Y."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Shi X."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Wang T."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Hu T."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Young N.L."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Nakada D."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Kitano A."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Konopleva M.Y."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Eagle K."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/author"Hoegenauer K.A."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/name"Blood"xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/pages"2183-2194"xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/title"AMP-activated protein kinase links acetyl-CoA homeostasis to BRD4 recruitment in acute myeloid leukemia."xsd:string
http://purl.uniprot.org/citations/31697807http://purl.uniprot.org/core/volume"134"xsd:string
http://purl.uniprot.org/citations/31697807http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31697807
http://purl.uniprot.org/citations/31697807http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31697807
http://purl.uniprot.org/uniprot/#_A0A2R8VHW4-mappedCitation-31697807http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31697807
http://purl.uniprot.org/uniprot/#_A0A494BBD0-mappedCitation-31697807http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31697807
http://purl.uniprot.org/uniprot/#_A0A494BAK1-mappedCitation-31697807http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31697807
http://purl.uniprot.org/uniprot/#_B0V2V6-mappedCitation-31697807http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31697807