| Literature DB >> 25533034 |
Lital Shaham1, Elena Vendramini2, Yubin Ge3, Yaron Goren4, Yehudit Birger5, Marloes R Tijssen6, Maureen McNulty7, Ifat Geron2, Omer Schwartzman2, Liat Goldberg5, Stella T Chou8, Holly Pitman3, Mitchell J Weiss8, Shulamit Michaeli9, Benjamin Sredni10, Berthold Göttgens6, John D Crispino7, Jeffrey W Taub11, Shai Izraeli2.
Abstract
Children with Down syndrome (DS) are at increased risk for acute myeloid leukemias (ML-DS) characterized by mixed megakaryocytic and erythroid phenotype and by acquired mutations in the GATA1 gene resulting in a short GATA1s isoform. The chromosome 21 microRNA (miR)-125b cluster has been previously shown to cooperate with GATA1s in transformation of fetal hematopoietic progenitors. In this study, we report that the expression of miR-486-5p is increased in ML-DS compared with non-DS acute megakaryocytic leukemias (AMKLs). miR-486-5p is regulated by GATA1 and GATA1s that bind to the promoter of its host gene ANK1. miR-486-5p is highly expressed in mouse erythroid precursors and knockdown (KD) in ML-DS cells reduced their erythroid phenotype. Ectopic expression and KD of miR-486-5p in primary fetal liver hematopoietic progenitors demonstrated that miR-486-5p cooperates with Gata1s to enhance their self renewal. Consistent with its activation of AKT, overexpression and KD experiments showed its importance for growth and survival of human leukemic cells. Thus, miR-486-5p cooperates with GATA1s in supporting the growth and survival, and the aberrant erythroid phenotype of the megakaryocytic leukemias of DS.Entities:
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Year: 2014 PMID: 25533034 PMCID: PMC4335082 DOI: 10.1182/blood-2014-06-581892
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113