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http://purl.uniprot.org/citations/24596420http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24596420http://www.w3.org/2000/01/rdf-schema#comment"Nucleophosmin-mutated acute myeloid leukemia (NPM1mut-AML) patients have a high rate of complete remission (CR) to induction chemotherapy. However, the mechanisms responsible for such effects are unknown. Because miR-10 family members are expressed at high levels in NPM1mut-AML, we evaluated whether these microRNAs could predict chemotherapy response in AML. We found that high baseline miR-10 family expression in 54 untreated cytogenetically heterogeneous AML patients was associated with achieving CR. However, when we included NPM1 mutation status in the multivariable model, there was a significant interaction effect between miR-10a-5p expression and NPM1 mutation status. Similar results were observed when using a second cohort of 183 cytogenetically normal older (age ≥ 60 years) AML patients. Loss- and gain-of-function experiments using miR-10a-5p in cell lines and primary blasts did not demonstrate any effect in apoptosis or cell proliferation at baseline or after chemotherapy. These data support a bystander role for the miR-10 family in NPM1mut-AML."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.org/dc/terms/identifier"doi:10.1182/blood-2013-10-532374"xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Huang X."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Yu X."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Volinia S."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Ranganathan P."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Andreeff M."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Croce C.M."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Bloomfield C.D."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Marcucci G."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Geyer S."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Kornblau S.M."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Garzon R."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Havelange V."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/author"Nicolet D."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/name"Blood"xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/pages"2412-2415"xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/title"Implications of the miR-10 family in chemotherapy response of NPM1-mutated AML."xsd:string
http://purl.uniprot.org/citations/24596420http://purl.uniprot.org/core/volume"123"xsd:string
http://purl.uniprot.org/citations/24596420http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/24596420
http://purl.uniprot.org/citations/24596420http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24596420
http://purl.uniprot.org/uniprot/#_A0A0G2JNH0-mappedCitation-24596420http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24596420
http://purl.uniprot.org/uniprot/#_A0A140VJQ2-mappedCitation-24596420http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24596420