Evidence map›Paper›PMID 30190546›Full record

ArticleOncogene2019

Premature activation of Cdk1 leads to mitotic events in S phase and embryonic lethality.

Radoslaw Szmyd, Joanna Niska-Blakie, M Kasim Diril, Patrícia Renck Nunes, Konstantinos Tzelepis, Aurélie Lacroix, Noémi van Hul, Lih-Wen Deng, Joao Matos, Oliver Dreesen and 2 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 65 citations in OpenAlex.

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  11. Autophagy modulates the stability of Wee1 and cell cycle G2/M transition.Biochemical and biophysical research communications · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 5 countries.

Radoslaw SzmydInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
Joanna Niska-BlakieInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
M Kasim DirilInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
Patrícia Renck NunesInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
Konstantinos TzelepisInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
Aurélie LacroixInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
Noémi van HulInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
Lih-Wen DengNational University of Singapore (NUS), Department of Biochemistry, Singapore, 117597, Republic of Singapore.
Joao MatosETH Zürich, Department of Biology, Zürich, Switzerland.
Oliver DreesenInstitute of Medical Biology, A*STAR, Singapore, 138648, Republic of Singapore.
Xavier BisteauInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore.
Philipp KaldisInstitute of Molecular and Cell Biology (IMCB), A*STAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos #3-09, Singapore, 138673, Republic of Singapore. kaldis@imcb.a-star.edu.sg.ORCID http://orcid.org/0000-0002-7247-7591
Agency for Science, Technology and Research · SGETH Zurich · CHNational University of Singapore · SG

Funding

A*STAR | Institute of Molecular and Cell Biology (Institute of Molecular and Cell Biology - A STAR) core
6 · The paper itself

Abstract

Cell cycle regulation, especially faithful DNA replication and mitosis, are crucial to maintain genome stability. Cyclin-dependent kinase (CDK)/cyclin complexes drive most processes in cellular proliferation. In response to DNA damage, cell cycle surveillance mechanisms enable normal cells to arrest and undergo repair processes. Perturbations in genomic stability can lead to tumor development and suggest that cell cycle regulators could be effective targets in anticancer therapy. However, many clinical trials ended in failure due to off-target effects of the inhibitors used. Here, we investigate in vivo the importance of WEE1- and MYT1-dependent inhibitory phosphorylation of mammalian CDK1. We generated Cdk1

Indexed as

MitosisS PhaseAmino Acid SubstitutionAnimalsCDC2 Protein KinaseCell Cycle ProteinsDNA-Binding ProteinsEmbryo LossEmbryo, MammalianEnzyme ActivationMiceMice, TransgenicMutation, MissenseNuclear ProteinsProtein-Tyrosine KinasesTranscription FactorsCDC2 Protein KinaseCdk1 protein, mouseCell Cycle ProteinsDNA-Binding ProteinsMyt1 protein, mouseNuclear ProteinsProtein-Tyrosine KinasesTranscription FactorsWee1 protein, mouse

Identifiers

PMID30190546
PMCPMC6756125
OpenAlexW2891992691

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.