Evidence map›Paper›PMID 37794795›Full record

ArticleHaematologica2024

Susceptibility of pediatric acute lymphoblastic leukemia to STAT3 inhibition depends on p53 induction.

Luca Gasparoli, Clemence Virely, Alexia Tsakaneli, Noelia Che, Darren Edwards, Jack Bartram, Michael Hubank, Deepali Pal, Olaf Heidenreich, Joost H A Martens and 2 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

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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

12 authors at 7 institutions in 2 countries.

Luca GasparoliCancer Section, Developmental Biology and Cancer Department, UCL Great Ormond Street Institute of Child Health, London.
Clemence VirelyCancer Section, Developmental Biology and Cancer Department, UCL Great Ormond Street Institute of Child Health, London.
Alexia TsakaneliCancer Section, Developmental Biology and Cancer Department, UCL Great Ormond Street Institute of Child Health, London.
Noelia CheCancer Section, Developmental Biology and Cancer Department, UCL Great Ormond Street Institute of Child Health, London.
Darren EdwardsDepartment of Paediatric Haematology, Great Ormond Street Hospital for Children, London.
Jack BartramDepartment of Paediatric Haematology, Great Ormond Street Hospital for Children, London.
Michael HubankCentre for Molecular Pathology, The Royal Marsden, Sutton.
Deepali PalDepartment of Applied Sciences, Northumbria University, Newcastle upon Tyne.
Olaf HeidenreichPrincess Maxima Centrum for Pediatric Oncology, Utrecht.
Joost H A MartensDepartment of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University, Nijmegen.
Jasper De BoerCancer Section, Developmental Biology and Cancer Department, UCL Great Ormond Street Institute of Child Health, London.
Owen WilliamsCancer Section, Developmental Biology and Cancer Department, UCL Great Ormond Street Institute of Child Health, London. owen.williams@ucl.ac.uk.
University College London · GBCRUK Lung Cancer Centre of Excellence · GBGreat Ormond Street Hospital · GBNorthumbria University · GBPrincess Máxima Center · NLRadboud Institute for Molecular Life Sciences · NLRoyal Marsden NHS Foundation Trust · GB

Funding

Medical Research Council MR/S021000/1
6 · The paper itself

Abstract

Advances in the clinical management of pediatric B-cell acute lymphoblastic leukemia (B-ALL) have dramatically improved outcomes for this disease. However, relapsed and high-risk disease still contribute to significant numbers of treatment failures. Development of new, broad range therapies is urgently needed for these cases. We previously reported the susceptibility of ETV6-RUNX1+ pediatric B-ALL to inhibition of signal transducer and activator of transcription 3 (STAT3) activity. In the present study, we demonstrate that pharmacological or genetic inhibition of STAT3 results in p53 induction and that CRISPR-mediated TP53 knockout substantially reverses susceptibility to STAT3 inhibition. Furthermore, we demonstrate that sensitivity to STAT3 inhibition in patient-derived xenograft (PDX) B-ALL samples is not restricted to any particular disease subtype, but rather depends on TP53 status, the only resistant samples being TP53 mutant. Induction of p53 following STAT3 inhibition is not directly dependent on MDM2 but correlates with degradation of MDM4. As such, STAT3 inhibition exhibits synergistic in vitro and in vivo anti-leukemia activity when combined with MDM2 inhibition. Taken together with the relatively low frequency of TP53 mutations in this disease, these data support the future development of combined STAT3/ MDM2 inhibition in the therapy of refractory and relapsed pediatric B-ALL.

Indexed as

Precursor B-Cell Lymphoblastic Leukemia-LymphomaCell Cycle ProteinsChildHumansProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2RecurrenceSTAT3 Transcription FactorTumor Suppressor Protein p53Cell Cycle ProteinsMDM4 protein, humanProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2STAT3 protein, humanSTAT3 Transcription FactorTumor Suppressor Protein p53

Identifiers

PMID37794795
PMCPMC10985450
OpenAlexW4387356811

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.