Evidence map›Paper›PMID 34570885›Full record

ArticleBlood2022

The megakaryocytic transcription factor ARID3A suppresses leukemia pathogenesis.

Oriol Alejo-Valle, Karoline Weigert, Raj Bhayadia, Michelle Ng, Hasan Issa, Christoph Beyer, Stephan Emmrich, Konstantin Schuschel, Christian Ihling, Andrea Sinz and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Blood, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 35 citations in OpenAlex.

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  13. Aberrant stem cell and developmental programs in pediatric leukemia.Frontiers in cell and developmental biology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 2 countries.

Oriol Alejo-VallePediatric Hematology and Oncology, Martin-Luther-University Halle-Wittenberg, Halle, Germany.ORCID 0000-0002-0988-7416
Karoline WeigertPediatric Hematology and Oncology, Martin-Luther-University Halle-Wittenberg, Halle, Germany.ORCID 0000-0002-0090-1250
Raj BhayadiaPediatric Hematology and Oncology, Department of Pediatrics, Goethe University Frankfurt, Frankfurt (Main), Germany.ORCID 0000-0003-0865-9582
Michelle NgPediatric Hematology and Oncology, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Hasan IssaPediatric Hematology and Oncology, Department of Pediatrics, Goethe University Frankfurt, Frankfurt (Main), Germany.ORCID 0000-0002-9760-9618
Christoph BeyerPediatric Hematology and Oncology, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Stephan EmmrichDepartment of Biology, University of Rochester, Rochester NY.ORCID 0000-0002-0537-4242
Konstantin SchuschelPediatric Hematology and Oncology, Department of Pediatrics, Goethe University Frankfurt, Frankfurt (Main), Germany.ORCID 0000-0002-5417-8950
Christian IhlingDepartment of Pharmaceutical Chemistry and Bioanalytics, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Andrea SinzDepartment of Pharmaceutical Chemistry and Bioanalytics, Institute of Pharmacy, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Martin ZimmermannPediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
Claudia WickenhauserInstitute of Pathology, University Hospital Halle, Halle, Germany.
Marius FlasinskiDepartment of Psychiatry, Psychosomatic Medicine and Psychotherapy, Hospital Tauberbischofsheim, Tauberbischofsheim, Germany.
Eniko RegenyiPediatric Hematology and Oncology, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Maurice LabuhnInstitute for Experimental Virology, Twincore, Center for Experimental and Clinical Infection Research, Hannover, Germany; and.
Dirk ReinhardtPediatric Hematology and Oncology, Pediatrics III, University Hospital Essen, Essen, Germany.ORCID 0000-0002-7027-4483
Marie-Laure YaspoMax Planck Institute for Molecular Genetics, Berlin, Germany.
Dirk HecklPediatric Hematology and Oncology, Martin-Luther-University Halle-Wittenberg, Halle, Germany.
Jan-Henning KlusmannPediatric Hematology and Oncology, Martin-Luther-University Halle-Wittenberg, Halle, Germany.ORCID 0000-0002-1070-0727
Martin Luther University Halle-Wittenberg · DEGoethe University Frankfurt · DEMax Planck Institute for Molecular Genetics · DECenter for Experimental and Clinical Infection Research · DEEssen University Hospital · DEMedizinische Hochschule Hannover · DEUniversity Hospital in Halle · DEUniversity of Rochester · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the plasticity of hematopoietic stem and progenitor cells, multiple routes of differentiation must be blocked in the the pathogenesis of acute myeloid leukemia, the molecular basis of which is incompletely understood. We report that posttranscriptional repression of the transcription factor ARID3A by miR-125b is a key event in the pathogenesis of acute megakaryoblastic leukemia (AMKL). AMKL is frequently associated with trisomy 21 and GATA1 mutations (GATA1s), and children with Down syndrome are at a high risk of developing the disease. The results of our study showed that chromosome 21-encoded miR-125b synergizes with Gata1s to drive leukemogenesis in this context. Leveraging forward and reverse genetics, we uncovered Arid3a as the main miR-125b target behind this synergy. We demonstrated that, during normal hematopoiesis, this transcription factor promotes megakaryocytic differentiation in concert with GATA1 and mediates TGFβ-induced apoptosis and cell cycle arrest in complex with SMAD2/3. Although Gata1s mutations perturb erythroid differentiation and induce hyperproliferation of megakaryocytic progenitors, intact ARID3A expression assures their megakaryocytic differentiation and growth restriction. Upon knockdown, these tumor suppressive functions are revoked, causing a blockade of dual megakaryocytic/erythroid differentiation and subsequently of AMKL. Inversely, restoring ARID3A expression relieves the arrest of megakaryocytic differentiation in AMKL patient-derived xenografts. This work illustrates how mutations in lineage-determining transcription factors and perturbation of posttranscriptional gene regulation can interact to block multiple routes of hematopoietic differentiation and cause leukemia. In AMKL, surmounting this differentiation blockade through restoration of the tumor suppressor ARID3A represents a promising strategy for treating this lethal pediatric disease.

Indexed as

AnimalsChildDNA-Binding ProteinsGATA1 Transcription FactorGene Expression Regulation, LeukemicGenes, Tumor SuppressorHumansLeukemia, Megakaryoblastic, AcuteMiceMice, Inbred C57BLMicroRNAsMutationTranscription FactorsARID3A protein, humanDNA-Binding ProteinsGATA1 protein, humanGATA1 Transcription FactorMicroRNAsMIRN125 microRNA, humanTranscription Factors

Identifiers

PMID34570885
PMCPMC9632760
OpenAlexW3203683891

What OpenQuestion holds

Textmetadata
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.