Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41467-017-00032-6
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dc.titleDisruption of the C/EBP? - MiR-182 balance impairs granulocytic differentiation
dc.contributor.authorWurm, A.A
dc.contributor.authorZjablovskaja, P
dc.contributor.authorKardosova, M
dc.contributor.authorGerloff, D
dc.contributor.authorBräuer-Hartmann, D
dc.contributor.authorKatzerke, C
dc.contributor.authorHartmann, J.-U
dc.contributor.authorBenoukraf, T
dc.contributor.authorFricke, S
dc.contributor.authorHilger, N
dc.contributor.authorMüller, A.-M
dc.contributor.authorBill, M
dc.contributor.authorSchwind, S
dc.contributor.authorTenen, D.G
dc.contributor.authorNiederwieser, D
dc.contributor.authorAlberich-Jorda, M
dc.contributor.authorBehre, G
dc.date.accessioned2020-10-20T10:31:08Z
dc.date.available2020-10-20T10:31:08Z
dc.date.issued2017
dc.identifier.citationWurm, A.A, Zjablovskaja, P, Kardosova, M, Gerloff, D, Bräuer-Hartmann, D, Katzerke, C, Hartmann, J.-U, Benoukraf, T, Fricke, S, Hilger, N, Müller, A.-M, Bill, M, Schwind, S, Tenen, D.G, Niederwieser, D, Alberich-Jorda, M, Behre, G (2017). Disruption of the C/EBP? - MiR-182 balance impairs granulocytic differentiation. Nature Communications 8 (1) : 32. ScholarBank@NUS Repository. https://doi.org/10.1038/s41467-017-00032-6
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178606
dc.description.abstractTranscription factor C/EBP? is a master regulator of myelopoiesis and its inactivation is associated with acute myeloid leukemia. Deregulation of C/EBP? by microRNAs during granulopoiesis or acute myeloid leukemia development has not been studied. Here we show that oncogenic miR-182 is a strong regulator of C/EBP?. Moreover, we identify a regulatory loop between C/EBP? and miR-182. While C/EBP? blocks miR-182 expression by direct promoter binding during myeloid differentiation, enforced expression of miR-182 reduces C/EBP? protein level and impairs granulopoiesis in vitro and in vivo. In addition, miR-182 expression is highly elevated particularly in acute myeloid leukemia patients with C-terminal CEBPA mutations, thereby depicting a mechanism by which C/EBP? blocks miR-182 expression. Furthermore, we present miR-182 expression as a prognostic marker in cytogenetically high-risk acute myeloid leukemia patients. Our data demonstrate the importance of a controlled balance between C/EBP? and miR-182 for the maintenance of healthy granulopoiesis. © 2017 The Author(s).
dc.publisherNature Publishing Group
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectCCAAT enhancer binding protein alpha
dc.subjectmicroRNA 182
dc.subjectCCAAT enhancer binding protein
dc.subjectCEBPA protein, human
dc.subjectCEBPA protein, mouse
dc.subjectmicroRNA
dc.subjectMirn182 microRNA, human
dc.subjectMirn182 microRNA, mouse
dc.subjectbiological development
dc.subjectcancer
dc.subjectchemical binding
dc.subjectgene expression
dc.subjectgenetic analysis
dc.subjectgenetic marker
dc.subjectlaboratory method
dc.subjectmutation
dc.subjectprotein
dc.subjectacute myeloid leukemia
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectArticle
dc.subjectbone marrow cell
dc.subjectcarboxy terminal sequence
dc.subjectcell differentiation
dc.subjectcontrolled study
dc.subjectdownstream processing
dc.subjectgene disruption
dc.subjectgene mutation
dc.subjectgene targeting
dc.subjectgranulocyte
dc.subjectgranulopoiesis
dc.subjecthuman
dc.subjecthuman cell
dc.subjectin vitro study
dc.subjectin vivo study
dc.subjectmouse
dc.subjectnonhuman
dc.subjectoncogene
dc.subjectpromoter region
dc.subjectanimal
dc.subjectcell differentiation
dc.subjectgenetics
dc.subjectknockout mouse
dc.subjectleukopoiesis
dc.subjectmetabolism
dc.subjectmortality
dc.subjectprognosis
dc.subjectreal time polymerase chain reaction
dc.subjectWestern blotting
dc.subjectAnimals
dc.subjectBlotting, Western
dc.subjectCCAAT-Enhancer-Binding Proteins
dc.subjectCell Differentiation
dc.subjectGranulocytes
dc.subjectHumans
dc.subjectLeukemia, Myeloid, Acute
dc.subjectLeukopoiesis
dc.subjectMice
dc.subjectMice, Knockout
dc.subjectMicroRNAs
dc.subjectPrognosis
dc.subjectReal-Time Polymerase Chain Reaction
dc.typeArticle
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.contributor.departmentMEDICINE
dc.description.doi10.1038/s41467-017-00032-6
dc.description.sourcetitleNature Communications
dc.description.volume8
dc.description.issue1
dc.description.page32
dc.published.statepublished
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