Item Type: | Article |
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Title: | Aberrant expression of miR-9/9* in myeloid progenitors inhibits neutrophil differentiation by post-transcriptional regulation of ERG |
Creators Name: | Nowek, K., Sun, S.M., Bullinger, L., Bindels, E.M.J., Exalto, C., Dijkstra, M.K., van Lom, K., Döhner, H., Erkeland, S.J., Löwenberg, B. and Jongen-Lavrencic, M. |
Abstract: | Aberrant post-transcriptional regulation by microRNAs (miRNAs) has been shown to be involved in the pathogenesis of acute myeloid leukemia (AML). In a previous study, we performed a large functional screen using a retroviral barcoded miRNA expression library. Here, we report that overexpression of miR-9/9* in myeloid 32D cell line (32D-miR-9/9*) had profound impact on granulocyte colony-stimulating factor-induced differentiation. Further in vitro studies showed that enforced expression of miR-9/9* blocked normal neutrophil development in 32D and in primary murine lineage-negative bone marrow cells. We examined the expression of miR-9/9* in a cohort of 647 primary human AMLs. In most cases, miR-9 and miR-9* were significantly upregulated and their expression levels varied according to AML subtype, with the highest expression in MLL-related leukemias harboring 11q23 abnormalities and the lowest expression in AML cases with t(8;21) and biallelic mutations in CEBPA. Gene expression profiling of AMLs with high expression of miR-9/9* and 32D-miR-9/9* identified ETS-related gene (Erg) as the only common potential target. Upregulation of ERG in 32D cells rescued miR-9/9*-induced block in neutrophil differentiation. Taken together, this study demonstrates that miR-9/9* are aberrantly expressed in most of AML cases and interfere with normal neutrophil differentiation by downregulation of ERG. |
Keywords: | Acute Myeloid Leukemia, Cell Differentiation, Inbred C57BL Mice, Leukemic Gene Expression Regulation, MicroRNAs, Myeloid Progenitor Cells, Neutrophils, Trans-Activators, Transcriptional Regulator ERG, Animals, Mice |
Source: | Leukemia |
ISSN: | 0887-6924 |
Publisher: | Nature Publishing Group |
Volume: | 30 |
Number: | 1 |
Page Range: | 229-37 |
Date: | January 2016 |
Official Publication: | https://doi.org/10.1038/leu.2015.183 |
PubMed: | View item in PubMed |
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