Evidence map›Paper›PMID 36902447›Full record

ArticleInternational journal of molecular sciences2023

Aurora B Kinase Inhibition by AZD1152 Concomitant with Tumor Treating Fields Is Effective in the Treatment of Cultures from Primary and Recurrent Glioblastomas.

Dietmar Krex, Paula Bartmann, Doris Lachmann, Alexander Hagstotz, Willi Jugel, Rosa S Schneiderman, Karnit Gotlib, Yaara Porat, Katja Robel, Achim Temme and 2 more

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In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
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.

Dietmar KrexDepartment of Neurosurgery, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Paula BartmannDepartment of Neurosurgery, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Doris LachmannDepartment of Neurosurgery, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Alexander HagstotzSection Experimental Neurosurgery/Tumor Immunology, Department of Neurosurgery, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Willi JugelSection Experimental Neurosurgery/Tumor Immunology, Department of Neurosurgery, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Rosa S SchneidermanNovocure® Ltd., 5 Nahum Het Street, Haifa 31905, Israel.
Karnit GotlibNovocure® Ltd., 5 Nahum Het Street, Haifa 31905, Israel.
Yaara PoratNovocure® Ltd., 5 Nahum Het Street, Haifa 31905, Israel.
Katja RobelSection Experimental Neurosurgery/Tumor Immunology, Department of Neurosurgery, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.
Achim TemmeGerman Cancer Consortium (DKTK), 01307 Dresden, Germany.ORCID 0000-0001-5084-1180
Moshe GiladiNovocure® Ltd., 5 Nahum Het Street, Haifa 31905, Israel.ORCID 0000-0003-1489-4175
Susanne MichenSection Experimental Neurosurgery/Tumor Immunology, Department of Neurosurgery, University Hospital Carl Gustav Carus, Technical University Dresden, 01307 Dresden, Germany.ORCID 0000-0002-5726-386X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor Treating Fields (TTFields) were incorporated into the treatment of glioblastoma, the most malignant brain tumor, after showing an effect on progression-free and overall survival in a phase III clinical trial. The combination of TTFields and an antimitotic drug might further improve this approach. Here, we tested the combination of TTFields with AZD1152, an Aurora B kinase inhibitor, in primary cultures of newly diagnosed (ndGBM) and recurrent glioblastoma (rGBM). AZD1152 concentration was titrated for each cell line and 5-30 nM were used alone or in addition to TTFields (1.6 V/cm RMS; 200 kHz) applied for 72 h using the inovitro™ system. Cell morphological changes were visualized by conventional and confocal laser microscopy. The cytotoxic effects were determined by cell viability assays. Primary cultures of ndGBM and rGBM varied in p53 mutational status; ploidy; EGFR expression and MGMT-promoter methylation status. Nevertheless; in all primary cultures; a significant cytotoxic effect was found following TTFields treatment alone and in all but one, a significant effect after treatment with AZD1152 alone was also observed. Moreover, in all primary cultures the combined treatment had the most pronounced cytotoxic effect in parallel with morphological changes. The combined treatment of TTFields and AZD1152 led to a significant reduction in the number of ndGBM and rGBM cells compared to each treatment alone. Further evaluation of this approach, which has to be considered as a proof of concept, is warranted, before entering into early clinical trials.

Indexed as

Antineoplastic AgentsGlioblastomaAurora Kinase BHumansNeoplasm Recurrence, LocalOrganophosphatesQuinazolines2-((3-((4-((5-(2-((3-fluorophenyl)amino)-2-oxoethyl)-1H-pyrazol-3-yl)amino)quinazolin-7-yl)oxy)propyl)(ethyl)amino)ethyl dihydrogen phosphateAntineoplastic AgentsAurora Kinase BOrganophosphatesQuinazolinesAurora B kinaseAZD1152glioblastomaprimary culturesTTFields

Identifiers

PMID36902447
PMCPMC10003311

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Registered trials

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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.