Evidence map›Paper›PMID 29880602›Full record

ArticleThe EMBO journal2018

Lmo2 expression defines tumor cell identity during T-cell leukemogenesis.

Idoia García-Ramírez, Sanil Bhatia, Guillermo Rodríguez-Hernández, Inés González-Herrero, Carolin Walter, Sara González de Tena-Dávila, Salma Parvin, Oskar Haas, Wilhelm Woessmann, Martin Stanulla and 18 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Cell Lineage Affiliation During Hematopoiesis.International journal of molecular sciences · 2025
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  8. The Social Norm of Hematopoietic Stem Cells and Dysregulation in Leukemia.International journal of molecular sciences · 2022
    Review
  9. Oncogenes and the Origins of Leukemias.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Lessons to cancer from studies of leukemia and hematopoiesis.Frontiers in cell and developmental biology · 2022
    Review
  12. Review
  13. Oncogenes, Proto-Oncogenes, and Lineage Restriction of Cancer Stem Cells.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Fli1Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. Article
  18. Hematopoietic Stem Cells: Nature and Niche Nurture.Bioengineering (Basel, Switzerland) · 2021
    Review
  19. The RARγ Oncogene: An Achilles Heel for Some Cancers.International journal of molecular sciences · 2021
    Review
  20. Review
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

28 authors at 12 institutions in 4 countries.

Idoia García-RamírezExperimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC-USAL, Salamanca, Spain.
Sanil BhatiaDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine University Dusseldorf, Dusseldorf, Germany.
Guillermo Rodríguez-HernándezExperimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC-USAL, Salamanca, Spain.
Inés González-HerreroExperimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC-USAL, Salamanca, Spain.
Carolin WalterInstitute of Medical Informatics, University of Muenster, Muenster, Germany.
Sara González de Tena-DávilaExperimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC-USAL, Salamanca, Spain.
Salma ParvinDivision of Hematology-Oncology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, USA.
Oskar HaasChildren's Cancer Research Institute, St Anna Children's Hospital, Vienna, Austria.
Wilhelm WoessmannDepartment of Pediatric Hematology and Oncology, Justus-Liebig-University Giessen, Giessen, Germany.
Martin StanullaPediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
Martin SchrappeDepartment of Pediatrics, Christian-Albrechts-University of Kiel and University Medical Center Schleswig-Holstein, Kiel, Germany.
Martin DugasInstitute of Medical Informatics, University of Muenster, Muenster, Germany.
Yasodha NatkunamDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Alberto OrfaoInstitute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain.
Verónica DomínguezTransgenesis Facility CNB-CBMSO, CSIC-UAM, Madrid, Spain.
Belén PintadoTransgenesis Facility CNB-CBMSO, CSIC-UAM, Madrid, Spain.
Oscar BlancoInstitute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain.
Diego Alonso-LópezBioinformatics Unit, Cancer Research Center (CSIC-USAL), Salamanca, Spain.
Javier De Las RivasInstitute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain.
Alberto Martín-LorenzoExperimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC-USAL, Salamanca, Spain.ORCID 0000-0003-0558-890X
Rafael JiménezInstitute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain.
Francisco Javier García CriadoInstitute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain.
María Begoña García CenadorInstitute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain.
Izidore S LossosDivision of Hematology-Oncology, Department of Medicine, Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL, USA.
Carolina Vicente-DueñasInstitute of Biomedical Research of Salamanca (IBSAL), Salamanca, Spain cvd@usal.es Arndt.Borkhardt@med.uni-duesseldorf.de Julia.Hauer@med.uni-duesseldorf.de isg@usal.es.ORCID 0000-0002-5401-8295
Arndt BorkhardtDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine University Dusseldorf, Dusseldorf, Germany cvd@usal.es Arndt.Borkhardt@med.uni-duesseldorf.de Julia.Hauer@med.uni-duesseldorf.de isg@usal.es.ORCID 0000-0002-6121-4737
Julia HauerDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine University Dusseldorf, Dusseldorf, Germany cvd@usal.es Arndt.Borkhardt@med.uni-duesseldorf.de Julia.Hauer@med.uni-duesseldorf.de isg@usal.es.ORCID 0000-0002-4058-3058
Isidro Sánchez-GarcíaExperimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC-USAL, Salamanca, Spain cvd@usal.es Arndt.Borkhardt@med.uni-duesseldorf.de Julia.Hauer@med.uni-duesseldorf.de isg@usal.es.ORCID 0000-0001-6989-9905
Instituto de Investigación Biomédica de Salamanca · ESUniversidad de Salamanca · ESHeinrich Heine University Düsseldorf · DECentro Nacional de Biotecnología · ESUniversity of Miami · USUniversity of Münster · DECentro de Investigación del Cáncer · ESChristian-Albrechts-Universität zu Kiel · DEJustus-Liebig-Universität Gießen · DEMedizinische Hochschule Hannover · DEStanford University · USSt Anna Children's Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The impact of LMO2 expression on cell lineage decisions during T-cell leukemogenesis remains largely elusive. Using genetic lineage tracing, we have explored the potential of LMO2 in dictating a T-cell malignant phenotype. We first initiated LMO2 expression in hematopoietic stem/progenitor cells and maintained its expression in all hematopoietic cells. These mice develop exclusively aggressive human-like T-ALL In order to uncover a potential exclusive reprogramming effect of LMO2 in murine hematopoietic stem/progenitor cells, we next showed that transient LMO2 expression is sufficient for oncogenic function and induction of T-ALL The resulting T-ALLs lacked LMO2 and its target-gene expression, and histologically, transcriptionally, and genetically similar to human LMO2-driven T-ALL We next found that during T-ALL development, secondary genomic alterations take place within the thymus. However, the permissiveness for development of T-ALL seems to be associated with wider windows of differentiation than previously appreciated. Restricted Cre-mediated activation of

Indexed as

CarcinogenesisCell Transformation, NeoplasticAdaptor Proteins, Signal TransducingAnimalsDisease Models, AnimalGene Expression ProfilingHematopoietic Stem CellsHistocytochemistryLIM Domain ProteinsMicePrecursor T-Cell Lymphoblastic Leukemia-LymphomaThymus GlandAdaptor Proteins, Signal TransducingLIM Domain ProteinsLmo2 protein, mousecancer initiationepigenetic primingmouse modelsoncogenesstem cells

Identifiers

PMID29880602
PMCPMC6043907
OpenAlexW2805756787

What OpenQuestion holds

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LicenceCC BY
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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.