Evidence map›Paper›PMID 31366618›Full record

ArticleBlood2019

LMO2 activation by deacetylation is indispensable for hematopoiesis and T-ALL leukemogenesis.

Tatsuya Morishima, Ann-Christin Krahl, Masoud Nasri, Yun Xu, Narges Aghaallaei, Betül Findik, Maksim Klimiankou, Malte Ritter, Marcus D Hartmann, Christian Johannes Gloeckner and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  6. The sirtuin family in health and disease.Signal transduction and targeted therapy · 2022
    Review
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  8. LMO2 expression is frequent in T-lymphoblastic leukemia and correlates with survival, regardless of T-cell stage.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Article
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  13. Fli1Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

24 authors at 6 institutions in 2 countries.

Tatsuya MorishimaDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.ORCID 0000-0003-3876-3217
Ann-Christin KrahlDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Masoud NasriDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Yun XuDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Narges AghaallaeiDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.ORCID 0000-0002-9890-3229
Betül FindikDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Maksim KlimiankouDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Malte RitterDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Marcus D HartmannDepartment of Protein Evolution, Max Planck Institute for Developmental Biology, Tübingen, Germany.ORCID 0000-0001-6937-5677
Christian Johannes GloecknerGerman Center for Neurodegenerative Diseases, Tübingen, Germany.ORCID 0000-0001-6494-6944
Sylwia StefanczykDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.ORCID 0000-0002-4134-4171
Christian LindnerDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Benedikt OswaldDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Regine BernhardDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Karin HähnelDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Ursula Hermanutz-KleinDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.
Martin EbingerUniversity Children's Hospital Tübingen, Tübingen, Germany.
Rupert HandgretingerUniversity Children's Hospital Tübingen, Tübingen, Germany.
Nicolas CasadeiInstitute of Medical Genetics and Applied Genomics, University Hospital Tübingen, Tübingen, Germany.ORCID 0000-0003-2209-0580
Karl WelteUniversity Children's Hospital Tübingen, Tübingen, Germany.
Maya AndreUniversity Children's Hospital Tübingen, Tübingen, Germany.
Patrick MüllerDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.ORCID 0000-0002-0702-6209
Baubak BajoghliDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.ORCID 0000-0002-7368-7523
Julia SkokowaDepartment of Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tübingen, Germany.ORCID 0000-0002-4399-2324
University Children's Hospital Tübingen · DEGerman Center for Neurodegenerative Diseases · DEMax Planck Institute for Developmental Biology · DEMax Planck Society · DEUniversity of Basel · CHUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic transcription factor LIM domain only 2 (LMO2), a member of the TAL1 transcriptional complex, plays an essential role during early hematopoiesis and is frequently activated in T-cell acute lymphoblastic leukemia (T-ALL) patients. Here, we demonstrate that LMO2 is activated by deacetylation on lysine 74 and 78 via the nicotinamide phosphoribosyltransferase (NAMPT)/sirtuin 2 (SIRT2) pathway. LMO2 deacetylation enables LMO2 to interact with LIM domain binding 1 and activate the TAL1 complex. NAMPT/SIRT2-mediated activation of LMO2 by deacetylation appears to be important for hematopoietic differentiation of induced pluripotent stem cells and blood formation in zebrafish embryos. In T-ALL, deacetylated LMO2 induces expression of TAL1 complex target genes

Indexed as

HematopoiesisAcetylationAdaptor Proteins, Signal TransducingAnimalsCells, CulturedHEK293 CellsHumansLeukopoiesisLIM Domain ProteinsMiceModels, MolecularPrecursor T-Cell Lymphoblastic Leukemia-LymphomaProto-Oncogene ProteinsTranscription FactorsZebrafishZebrafish ProteinsAdaptor Proteins, Signal TransducingLIM Domain ProteinsLMO2 protein, humanlmo2 protein, zebrafishProto-Oncogene ProteinsTranscription FactorsZebrafish Proteins

Identifiers

PMID31366618
PMCPMC6888148
OpenAlexW2966578705

What OpenQuestion holds

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Registered trials

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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.