Evidence map›Paper›PMID 26990877›Full record

ArticlePLoS genetics2016

MiR144/451 Expression Is Repressed by RUNX1 During Megakaryopoiesis and Disturbed by RUNX1/ETO.

Nicole Kohrs, Stephan Kolodziej, Olga N Kuvardina, Julia Herglotz, Jasmin Yillah, Stefanie Herkt, Alexander Piechatzek, Gabriela Salinas Riester, Thomas Lingner, Christian Wichmann and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  3. Transcription Factor TAL1 in Erythropoiesis.Advances in experimental medicine and biology · 2024
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  6. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 1 country.

Nicole KohrsGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Stephan KolodziejGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Olga N KuvardinaGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Julia HerglotzHeinrich-Pette-Institute, Leibniz Institute for Experimental Virology, Hamburg, Germany.
Jasmin YillahGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Stefanie HerktGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Alexander PiechatzekGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Gabriela Salinas RiesterMedical-University Goettingen, Transcriptome Analysis Laboratory, Goettingen, Germany.
Thomas LingnerMedical-University Goettingen, Transcriptome Analysis Laboratory, Goettingen, Germany.
Christian WichmannDepartment of Transfusion Medicine, Cell Therapeutics and Hemostaseology, Ludwig-Maximilian University Hospital, Munich, Germany.
Halvard BonigInstitute for Transfusion Medicine and Immunohematology, Johann-Wolfgang-Goethe University and German Red Cross Blood Service, Frankfurt am Main, Germany.
Erhard SeifriedInstitute for Transfusion Medicine and Immunohematology, Johann-Wolfgang-Goethe University and German Red Cross Blood Service, Frankfurt am Main, Germany.
Uwe PlatzbeckerDepartment of Hematology, Medical Clinic and Polyclinic I, University Hospital Carl Gustav Carus, Dresden, Germany.
Hind MedyoufGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Manuel GrezGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Jörn LausenGeorg-Speyer-Haus, Institute for Tumorbiology and Experimental Therapy, Frankfurt, Germany.
Georg Speyer Haus · DEGoethe University Frankfurt · DEUniversity of Göttingen · DEGerman Red Cross · DELeibniz Institute of Virology (LIV) · DELudwig-Maximilians-Universität München · DEUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A network of lineage-specific transcription factors and microRNAs tightly regulates differentiation of hematopoietic stem cells along the distinct lineages. Deregulation of this regulatory network contributes to impaired lineage fidelity and leukemogenesis. We found that the hematopoietic master regulator RUNX1 controls the expression of certain microRNAs, of importance during erythroid/megakaryocytic differentiation. In particular, we show that the erythorid miR144/451 cluster is epigenetically repressed by RUNX1 during megakaryopoiesis. Furthermore, the leukemogenic RUNX1/ETO fusion protein transcriptionally represses the miR144/451 pre-microRNA. Thus RUNX1/ETO contributes to increased expression of miR451 target genes and interferes with normal gene expression during differentiation. Furthermore, we observed that inhibition of RUNX1/ETO in Kasumi1 cells and in RUNX1/ETO positive primary acute myeloid leukemia patient samples leads to up-regulation of miR144/451. RUNX1 thus emerges as a key regulator of a microRNA network, driving differentiation at the megakaryocytic/erythroid branching point. The network is disturbed by the leukemogenic RUNX1/ETO fusion product.

Indexed as

Cell DifferentiationCell LineageCore Binding Factor Alpha 2 SubunitGene Expression Regulation, LeukemicGene Regulatory NetworksHumansLeukemia, Myeloid, AcuteMegakaryocytesMicroRNAsOncogene Proteins, FusionCore Binding Factor Alpha 2 SubunitMicroRNAsMIRN451 microRNA, humanOncogene Proteins, FusionRUNX1 protein, human

Identifiers

PMID26990877
PMCPMC4798443
OpenAlexW2302718136

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.