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http://purl.uniprot.org/citations/20227367http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20227367http://www.w3.org/2000/01/rdf-schema#comment"To sustain tumor growth, cancer cells must be able to adapt to fluctuations in energy availability. We have identified a single microRNA that controls glioma cell proliferation, migration, and responsiveness to glucose deprivation. Abundant glucose allows relatively high miR-451 expression, promoting cell growth. In low glucose, miR-451 levels decrease, slowing proliferation but enhancing migration and survival. This allows cells to survive metabolic stress and seek out favorable growth conditions. In glioblastoma patients, elevated miR-451 is associated with shorter survival. The effects of miR-451 are mediated by LKB1, which it represses through targeting its binding partner, CAB39 (MO25 alpha). Overexpression of miR-451 sensitized cells to glucose deprivation, suggesting that its downregulation is necessary for robust activation of LKB1 in response to metabolic stress. Thus, miR-451 is a regulator of the LKB1/AMPK pathway, and this may represent a fundamental mechanism that contributes to cellular adaptation in response to altered energy availability."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.org/dc/terms/identifier"doi:10.1016/j.molcel.2010.02.018"xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Ostrowski M.C."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Bronisz A."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Godlewski J."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Chiocca E.A."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Nowicki M.O."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Nuovo G."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Palatini J."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"De Lay M."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Lawler S.E."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/author"Van Brocklyn J."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/name"Mol Cell"xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/pages"620-632"xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/title"MicroRNA-451 regulates LKB1/AMPK signaling and allows adaptation to metabolic stress in glioma cells."xsd:string
http://purl.uniprot.org/citations/20227367http://purl.uniprot.org/core/volume"37"xsd:string
http://purl.uniprot.org/citations/20227367http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20227367
http://purl.uniprot.org/citations/20227367http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/20227367
http://purl.uniprot.org/uniprot/#_D4P556-mappedCitation-20227367http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20227367
http://purl.uniprot.org/uniprot/#_A0A0S2Z4C7-mappedCitation-20227367http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20227367
http://purl.uniprot.org/uniprot/#_A0A0S2Z4D1-mappedCitation-20227367http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20227367
http://purl.uniprot.org/uniprot/#_A6YR18-mappedCitation-20227367http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20227367
http://purl.uniprot.org/uniprot/#_Q15831-mappedCitation-20227367http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/20227367