Evidence map›Paper›PMID 35253392›Full record

ArticleEMBO molecular medicine2022

CDK7/12/13 inhibition targets an oscillating leukemia stem cell network and synergizes with venetoclax in acute myeloid leukemia.

Lixiazi He, Christian Arnold, Judith Thoma, Christian Rohde, Maksim Kholmatov, Swati Garg, Cheng-Chih Hsiao, Linda Viol, Kaiqing Zhang, Rui Sun and 17 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Complex G-protein signaling of the adhesion GPCR, ADGRA3.The Journal of biological chemistry · 2025
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  9. Cyclin-dependent kinases: Masters of the eukaryotic universe.Wiley interdisciplinary reviews. RNA · 2023
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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

27 authors at 7 institutions in 5 countries.

Lixiazi HeDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
Christian ArnoldMolecular Medicine Partnership Unit (MMPU), University of Heidelberg and European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Judith ThomaPhysical Chemistry of Biosystems, Institute of Physical Chemistry, Heidelberg University, Heidelberg, Germany.
Christian RohdeDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
Maksim KholmatovMolecular Medicine Partnership Unit (MMPU), University of Heidelberg and European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Swati GargDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
Cheng-Chih HsiaoDepartment of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam University Medical Centers, Amsterdam, Netherlands.
Linda ViolCentre for Organismal Studies (COS)/Centre for Cell and Molecular Biology (ZMBH), University of Heidelberg, Heidelberg, Germany.
Kaiqing ZhangDivision of Molecular Embryology, DKFZ-ZMBH Alliance, Heidelberg, Germany.ORCID 0000-0003-0213-6035
Rui SunDivision of Molecular Embryology, DKFZ-ZMBH Alliance, Heidelberg, Germany.
Christina SchmidtDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
Maike JanssenDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
Tara MacRaeLaboratory of Molecular Genetics of Stem Cells, Institute for Research in Immunology and Cancer, University of Montreal, Montreal, Quebec, Canada.
Karin HuberDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
Christian ThiedeDepartment of Internal Medicine I, University Hospital of Dresden Carl Gustav Carus, Dresden, Germany.ORCID 0000-0003-1241-2048
Josée HébertThe Quebec Leukemia Cell Bank and Division of Hematology-Oncology, Maisonneuve-Rosemont Hospital, Montréal, Canada.
Guy SauvageauLaboratory of Molecular Genetics of Stem Cells, Institute for Research in Immunology and Cancer, University of Montreal, Montreal, Quebec, Canada.
Julia SpratteDepartment of Gynecology and Obstetrics, University Hospital Heidelberg, Heidelberg, Germany.
Herbert FluhrDepartment of Gynecology and Obstetrics, University Hospital Heidelberg, Heidelberg, Germany.
Gabriela AustDepartment of Surgery, Research Laboratories, Leipzig University, Leipzig, Germany.
Carsten Müller-TidowDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.
Christof NiehrsDivision of Molecular Embryology, DKFZ-ZMBH Alliance, Heidelberg, Germany.
Gislene PereiraCentre for Organismal Studies (COS)/Centre for Cell and Molecular Biology (ZMBH), University of Heidelberg, Heidelberg, Germany.ORCID 0000-0002-6519-4737
Jörg HamannDepartment of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam University Medical Centers, Amsterdam, Netherlands.ORCID 0000-0002-9448-1727
Motomu TanakaPhysical Chemistry of Biosystems, Institute of Physical Chemistry, Heidelberg University, Heidelberg, Germany.ORCID 0000-0003-3663-9554
Judith B ZauggMolecular Medicine Partnership Unit (MMPU), University of Heidelberg and European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.ORCID 0000-0001-8324-4040
Caroline PabstDepartment of Medicine V, Hematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.ORCID 0000-0001-9716-5909
Heidelberg University · DEAmsterdam University Medical Centers · NLHôpital Maisonneuve-Rosemont · CAInstitute for Research in Immunology and Cancer · CAKyoto University · JPLeipzig University · DEUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The heterogeneous response of acute myeloid leukemia (AML) to current anti-leukemic therapies is only partially explained by mutational heterogeneity. We previously identified GPR56 as a surface marker associated with poor outcome across genetic groups, which characterizes two leukemia stem cell (LSC)-enriched compartments with different self-renewal capacities. How these compartments self-renew remained unclear. Here, we show that GPR56

Indexed as

Bridged Bicyclo Compounds, HeterocyclicCyclin-Dependent KinasesLeukemia, Myeloid, AcuteProtein Kinase InhibitorsSulfonamidesAntineoplastic Combined Chemotherapy ProtocolsCDC2 Protein KinaseCyclin-Dependent Kinase-Activating KinaseDrug SynergismHedgehog ProteinsHumansNeoplastic Stem CellsProto-Oncogene Proteins c-bcl-2Bridged Bicyclo Compounds, HeterocyclicCDC2 Protein KinaseCDK12 protein, humanCDK13 protein, humanCDK7 protein, humanCyclin-Dependent Kinase-Activating KinaseCyclin-Dependent KinasesHedgehog ProteinsProtein Kinase InhibitorsProto-Oncogene Proteins c-bcl-2SulfonamidesvenetoclaxAMLCDK7 inhibitionGPR56leukemia stem cellself-renewal

Identifiers

PMID35253392
PMCPMC8988201
OpenAlexW4220884427

What OpenQuestion holds

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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.