Evidence map›Paper›PMID 33737511›Full record

ArticleBlood cancer journal2021

HSP90 inhibitor NVP-BEP800 affects stability of SRC kinases and growth of T-cell and B-cell acute lymphoblastic leukemias.

Rony Mshaik, John Simonet, Aleksandra Georgievski, Layla Jamal, Shaliha Bechoua, Paola Ballerini, Pierre-Simon Bellaye, Zandile Mlamla, Jean-Paul Pais de Barros, Audrey Geissler and 4 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Targeting proteostasis pathways for cancer therapy.Journal of pharmaceutical analysis · 2025
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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

14 authors at 4 institutions in 1 country.

Rony MshaikUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
John SimonetUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Aleksandra GeorgievskiUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Layla JamalUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Shaliha BechouaCentre de Ressources Biologiques Ferdinand Cabanne, Hôpital Universitaire François Mitterrand, Dijon, France.
Paola BalleriniLaboratoire d'Hématologie, Assistance Publique Hôpitaux de Paris, Hôpital Armand Trousseau, Paris, France.
Pierre-Simon BellayeUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Zandile MlamlaUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Jean-Paul Pais de BarrosUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Audrey GeisslerPlateforme d'Imagerie Cellulaire, CellImaP, Université de Bourgogne Franche-Comté, Dijon, France.
Pierre-Jean FrancinLaboratoire de Génétique Chromosomique et Moléculaire, Plateau Technique de Biologie, Hôpital Universitaire François Mitterrand, Dijon, France.
François GirodonUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Carmen GarridoUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France.
Ronan QuéréUMR1231, Inserm, Université de Bourgogne Franche-Comté, Dijon, France. ronan.quere@inserm.fr.ORCID 0000-0002-1615-6769
Inserm · FRLaboratoire de Génétique Cellulaire · FRSorbonne Université · FRUniversité de Bourgogne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell and B-cell acute lymphoblastic leukemias (T-ALL, B-ALL) are aggressive hematological malignancies characterized by an accumulation of immature T- or B-cells. Although patient outcomes have improved, novel targeted therapies are needed to reduce the intensity of chemotherapy and improve the prognosis of high-risk patients. Using cell lines, primary cells and patient-derived xenograft (PDX) models, we demonstrate that ALL cells viability is sensitive to NVP-BEP800, an ATP-competitive inhibitor of Heat shock protein 90 (HSP90). Furthermore, we reveal that lymphocyte-specific SRC family kinases (SFK) are important clients of the HSP90 chaperone in ALL. When PDX mice are treated with NVP-BEP800, we found that there is a decrease in ALL progression. Together, these results demonstrate that the chaperoning of SFK by HSP90 is involved in the growth of ALL. These novel findings provide an alternative approach to target SRC kinases and could be used for the development of new treatment strategies for ALL.

Indexed as

AnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationEnzyme StabilityHSP90 Heat-Shock ProteinsHumansMiceMice, Inbred NODMice, SCIDPrecursor Cell Lymphoblastic Leukemia-LymphomaPyrimidinessrc-Family KinasesTumor Cells, CulturedAntineoplastic AgentsHSP90 Heat-Shock ProteinsNVP-BEP800Pyrimidinessrc-Family Kinases

Identifiers

PMID33737511
PMCPMC7973815
OpenAlexW3136375216

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.