Evidence map›Paper›PMID 30050105›Full record

ArticleCell death & disease2018

MicroRNA-143 targets ERK5 in granulopoiesis and predicts outcome of patients with acute myeloid leukemia.

Jens-Uwe Hartmann, Daniela Bräuer-Hartmann, Miroslava Kardosova, Alexander A Wurm, Franziska Wilke, Cindy Schödel, Dennis Gerloff, Christiane Katzerke, Rosanna Krakowsky, Carolina Yaeko Namasu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. VCAN Is Essential for ERK5-Driven Tumorigenesis in Soft Tissue Sarcoma.International journal of biological sciences · 2026
    Article
  2. MircoRNAs predict and modulate responses to chemotherapy in leukemic patients.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    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 4 institutions in 2 countries.

Jens-Uwe HartmannDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Daniela Bräuer-HartmannDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Miroslava KardosovaInstitute of Molecular Genetics of the ASCR, v.v.i. Laboratory of Haematooncology, Prague, Czech Republic.
Alexander A WurmDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Franziska WilkeDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Cindy SchödelDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Dennis GerloffDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Christiane KatzerkeDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Rosanna KrakowskyDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Carolina Yaeko NamasuDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Marius BillDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Sebastian SchwindDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Carsten Müller-TidowDepartment of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.
Dietger NiederwieserDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany.
Meritxell Alberich-JordaInstitute of Molecular Genetics of the ASCR, v.v.i. Laboratory of Haematooncology, Prague, Czech Republic.
Gerhard BehreDivision of Hematology and Oncology, Leipzig University Hospital, Leipzig, Germany. Gerhard.Behre@medizin.uni-leipzig.de.
University Hospital Leipzig · DELeipzig University · DECzech Academy of Sciences, Institute of Molecular Genetics · CZHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoiesis, the formation of blood cells from hematopoietic stem cells (HSC), is a highly regulated process. Since the discovery of microRNAs (miRNAs), several studies have shown their significant role in the regulation of the hematopoietic system. Impaired expression of miRNAs leads to disrupted cellular pathways and in particular causes loss of hematopoietic ability. Here, we report a previously unrecognized function of miR-143 in granulopoiesis. Hematopoietic cells undergoing granulocytic differentiation exhibited increased miR-143 expression. Overexpression or ablation of miR-143 expression resulted in accelerated granulocytic differentiation or block of differentiation, respectively. The absence of miR-143 in mice resulted in a reduced number of mature granulocytes in blood and bone marrow. Additionally, we observed an association of high miR-143 expression levels with a higher probability of survival in two different cohorts of patients with acute myeloid leukemia (AML). Overexpression of miR-143 in AML cells impaired cell growth, partially induced differentiation, and caused apoptosis. Argonaute2-RNA-Immunoprecipitation assay revealed ERK5, a member of the MAPK-family, as a target of miR-143 in myeloid cells. Further, we observed an inverse correlation of miR-143 and ERK5 in primary AML patient samples, and in CD34

Indexed as

3' Untranslated RegionsAnimalsAntagomirsApoptosisCell DifferentiationCell ProliferationGranulocytesHematopoietic Stem CellsHumansLeukemia, Myeloid, AcuteMiceMice, Inbred C57BLMicroRNAsMitogen-Activated Protein Kinase 7PrognosisSurvival Rate3' Untranslated RegionsAntagomirsMAPK7 protein, humanMicroRNAsMIRN143 microRNA, humanMitogen-Activated Protein Kinase 7

Identifiers

PMID30050105
PMCPMC6062564
OpenAlexW2883572600

What OpenQuestion holds

Textmetadata
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.