Evidence map›Paper›PMID 30859681›Full record

ArticleMolecular oncology2019

In vitro study of the Polo-like kinase 1 inhibitor volasertib in non-small-cell lung cancer reveals a role for the tumor suppressor p53.

Jolien Van den Bossche, Christophe Deben, Ines De Pauw, Hilde Lambrechts, Christophe Hermans, Vanessa Deschoolmeester, Julie Jacobs, Pol Specenier, Patrick Pauwels, Jan Baptist Vermorken and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  9. Review
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  11. Observational
  12. Article
  13. Mitotic Poisons in Research and Medicine.Molecules (Basel, Switzerland) · 2020
    Review
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  15. Review
  16. Article
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

13 authors at 2 institutions in 1 country.

Jolien Van den BosscheCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Christophe DebenCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.ORCID 0000-0001-8085-2040
Ines De PauwCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Hilde LambrechtsCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Christophe HermansCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Vanessa DeschoolmeesterCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Julie JacobsCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Pol SpecenierDepartment of Oncology, Antwerp University Hospital, Edegem, Belgium.
Patrick PauwelsCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Jan Baptist VermorkenCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Marc PeetersCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
Filip LardonCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
An WoutersCenter for Oncological Research (CORE), University of Antwerp, Wilrijk, Belgium.
University of Antwerp · BEAntwerp University Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polo-like kinase 1 (Plk1), a master regulator of mitosis and the DNA damage response, is considered to be an intriguing target in the research field of mitotic intervention. The observation that Plk1 is overexpressed in multiple human malignancies, including non-small-cell lung cancer (NSCLC), gave rise to the development of several small-molecule inhibitors. Volasertib, presently the most extensively studied Plk1 inhibitor, has been validated to efficiently reduce tumor growth in preclinical settings. Unfortunately, only modest antitumor activity against solid tumors was reported in clinical trials. This discrepancy prompted research into the identification of predictive biomarkers. In this study, we investigated the therapeutic effect of volasertib monotherapy (i.e., cytotoxicity, cell cycle distribution, apoptotic cell death, cellular senescence, and migration) in a panel of NSCLC cell lines differing in p53 status under both normal and reduced oxygen tension (<0.1% O

Indexed as

A549 CellsApoptosisBiomarkers, TumorCarcinoma, Non-Small-Cell LungCell Cycle ProteinsCell HypoxiaGene Knockdown TechniquesHumansLung NeoplasmsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsPteridinesTumor Suppressor Protein p53BI 6727Biomarkers, TumorCell Cycle ProteinsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsPteridinesTP53 protein, humanTumor Suppressor Protein p53hypoxianon-small-cell lung cancerp53Polo-like kinase 1senescencevolasertib

Identifiers

PMID30859681
PMCPMC6487694
OpenAlexW2921653938

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.