Evidence map›Paper›PMID 30467206›Full record

ArticleHaematologica2019

Targeting intermediary metabolism enhances the efficacy of BH3 mimetic therapy in hematologic malignancies.

Aoula Al-Zebeeby, Meike Vogler, Mateus Milani, Caitlin Richards, Ahoud Alotibi, Georgia Greaves, Martin J S Dyer, Gerald M Cohen, Shankar Varadarajan

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. A guide to B cell metabolism.Nature reviews. Immunology · 2026
    Review
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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

9 authors at 3 institutions in 2 countries.

Aoula Al-ZebeebyDepartment of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK.
Meike VoglerInstitute for Experimental Cancer Research in Pediatrics, Goethe-University, Frankfurt, Germany.
Mateus MilaniDepartment of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK.
Caitlin RichardsDepartment of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK.
Ahoud AlotibiDepartment of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK.
Georgia GreavesDepartment of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK.
Martin J S DyerErnest and Helen Scott Haematological Research Institute, Leicester Cancer Research Centre, University of Leicester, Leicester Royal Infirmary, UK.
Gerald M CohenDepartment of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK.
Shankar VaradarajanDepartment of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, UK svar@liverpool.ac.uk.
University of Liverpool · GBFrankfurt Cancer Institute · DEUniversity of Leicester · GB

Funding

Medical Research Council MC_U132670597
6 · The paper itself

Abstract

BH3 mimetics are novel targeted drugs with remarkable specificity, potency and enormous potential to improve cancer therapy. However, acquired resistance is an emerging problem. We report the rapid development of resistance in chronic lymphocytic leukemia cells isolated from patients exposed to increasing doses of navitoclax (ABT-263), a BH3 mimetic. To mimic such rapid development of chemoresistance, we developed simple resistance models to three different BH3 mimetics, targeting BCL-2 (ABT-199), BCL-X

Indexed as

BiomimeticsDrug Resistance, NeoplasmAntineoplastic Agentsbcl-X ProteinBenzothiazolesBridged Bicyclo Compounds, HeterocyclicCholesterolClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicGlutamineHumansIndolesIsoquinolinesLeukemia, Lymphocytic, Chronic, B-CellLipogenesisMyeloid Cell Leukemia Sequence 1 ProteinA-1210477A-1331852Antineoplastic AgentsBax protein (53-86)BCL2L1 protein, humanBCL2 protein, humanbcl-X ProteinBenzothiazolesBridged Bicyclo Compounds, HeterocyclicCholesterolGlutamineIndolesIsoquinolinesMCL1 protein, humanMTOR protein, humanMyeloid Cell Leukemia Sequence 1 ProteinPeptide FragmentsProto-Oncogene ProteinsProto-Oncogene Proteins c-bcl-2SulfonamidesTOR Serine-Threonine Kinasesvenetoclax

Identifiers

PMID30467206
PMCPMC6518917
OpenAlexW2900566378

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.