Evidence map›Paper›PMID 31761618›Full record

ArticleEBioMedicine2019

CDK4/CDK6 inhibition as a novel strategy to suppress the growth and survival of BCR-ABL1

Mathias Schneeweiss-Gleixner, Konstantin Byrgazov, Gabriele Stefanzl, Daniela Berger, Gregor Eisenwort, Chantal Blanche Lucini, Susanne Herndlhofer, Sandra Preuner, Klara Obrova, Petra Pusic and 8 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Chronic Myeloid Leukemia and the T315IInternational journal of molecular sciences · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Resistance mutations in CML and how we approach them.Hematology. American Society of Hematology. Education Program · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. 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

18 authors at 4 institutions in 2 countries.

Mathias Schneeweiss-GleixnerDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria; Ludwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria.
Konstantin ByrgazovChildren's Cancer Research Institute (CCRI), Vienna, Austria.
Gabriele StefanzlLudwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria.
Daniela BergerLudwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria.
Gregor EisenwortDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria; Ludwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria.
Chantal Blanche LuciniChildren's Cancer Research Institute (CCRI), Vienna, Austria.
Susanne HerndlhoferDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria; Ludwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria.
Sandra PreunerChildren's Cancer Research Institute (CCRI), Vienna, Austria.
Klara ObrovaChildren's Cancer Research Institute (CCRI), Vienna, Austria.
Petra PusicChildren's Cancer Research Institute (CCRI), Vienna, Austria.
Nadine WitzenederLudwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria; Department of Laboratory Medicine, Medical University of Vienna, Austria.
Georg GreinerLudwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria; Department of Laboratory Medicine, Medical University of Vienna, Austria.
Gregor HoermannLudwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria; Department of Laboratory Medicine, Medical University of Vienna, Austria; Central Institute of Medical and Chemical Laboratory Diagnostics, University Hospital Innsbruck, Austria.
Wolfgang R SperrDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria; Ludwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria.
Thomas LionChildren's Cancer Research Institute (CCRI), Vienna, Austria.
Michael DeiningerDivision of Hematology and Hematologic Malignancies, Department of Internal Medicine, University of Utah, Salt Lake City, UT, USA.
Peter ValentDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria; Ludwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria. Electronic address: peter.valent@meduniwien.ac.at.
Karoline V GleixnerDepartment of Internal Medicine I, Division of Hematology & Hemostaseology, Medical University of Vienna, Waehringer Guertel 18-20, 1090 Vienna, Austria; Ludwig Boltzmann Institute for Hematology & Oncology, Medical University of Vienna, Austria. Electronic address: karoline.gleixner@meduniwien.ac.at.
Medical University of Vienna · ATLudwig Boltzmann Institute Applied Diagnostics · ATLudwig Boltzmann Institute for Cancer Research · ATUniversity of Utah · US

Funding

Austrian Science Fund FWF P 30625
6 · The paper itself

Abstract

purposePonatinib is the only approved tyrosine kinase inhibitor (TKI) suppressing BCR-ABL1

methodsViability, apoptosis and proliferation of drug-exposed primary CML cells and BCR-ABL1+ cell lines were examined by flow cytometry and

findingsHU was more effective in inhibiting the proliferation of leukemic cells harboring BCR-ABL1

interpretationHU and the CDK4/CDK6-blocker palbociclib inhibit growth of CML clones expressing BCR-ABL1

fundingThis project was supported by the Austrian Science Funds (FWF) projects F4701-B20, F4704-B20 and P30625.

Indexed as

MutationAdultAgedApoptosisCell CycleCell Line, TumorCell ProliferationCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Dose-Response Relationship, DrugDrug Resistance, NeoplasmDrug SynergismFemaleFusion Proteins, bcr-ablHumansHydroxyureaBCR-ABL1 fusion protein, humanCDK4 protein, humanCDK6 protein, humanCyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Fusion Proteins, bcr-ablHydroxyureaImidazolesponatinibProtein Kinase InhibitorsPyridazinesBCR-ABL1 mutationsCDK4/CDK6 – PalbociclibCMLHydroxyureaTKI resistance

Identifiers

PMID31761618
PMCPMC6921367
OpenAlexW2991308246

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.