Evidence map›Paper›PMID 29581894›Full record

ArticleCell death discovery2018

Genetic and pharmacological inhibition of Cdk1 provides neuroprotection towards ischemic neuronal death.

Quentin Marlier, Florian Jibassia, Sébastien Verteneuil, Jérôme Linden, Philipp Kaldis, Laurent Meijer, Laurent Nguyen, Renaud Vandenbosch, Brigitte Malgrange

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  5. Article
  6. Review
  7. Article
  8. Article
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  11. Review
  12. Article
  13. Review
  14. The Role of CDKs and CDKIs in Murine Development.International journal of molecular sciences · 2020
    Review
  15. Cell Cycle Proteins as Key Regulators of Postmitotic Cell Death.The Yale journal of biology and medicine · 2019
    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

9 authors at 3 institutions in 3 countries.

Quentin Marlier1Laboratory of Developmental Neurobiology, GIGA-Neurosciences, University of Liège, C.H.U. B36, 4000 Liège, Belgium.
Florian Jibassia1Laboratory of Developmental Neurobiology, GIGA-Neurosciences, University of Liège, C.H.U. B36, 4000 Liège, Belgium.
Sébastien Verteneuil1Laboratory of Developmental Neurobiology, GIGA-Neurosciences, University of Liège, C.H.U. B36, 4000 Liège, Belgium.
Jérôme Linden2Department of Psychology, University of Liege, B32, 4000 Liège, Belgium.
Philipp Kaldis3Institute of Molecular and Cell Biology (IMCB), ASTAR (Agency for Science, Technology and Research), 61 Biopolis Drive, Proteos#3-09, Singapore, 138673 Republic of Singapore.ORCID 0000-0002-7247-7591
Laurent MeijerManRos Therapeutics, Centre de Perharidy, 29680 Roscoff, France.
Laurent Nguyen6Laboratory of Molecular Regulation of Neurogenesis, GIGA-Neurosciences, University of Liège, C.H.U. B36, 4000 Liège, Belgium.ORCID 0000-0002-8560-3008
Renaud Vandenbosch1Laboratory of Developmental Neurobiology, GIGA-Neurosciences, University of Liège, C.H.U. B36, 4000 Liège, Belgium.
Brigitte Malgrange1Laboratory of Developmental Neurobiology, GIGA-Neurosciences, University of Liège, C.H.U. B36, 4000 Liège, Belgium.ORCID 0000-0002-8957-2528
University of Liège · BEAgency for Science, Technology and Research · SGManRos Therapeutics (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell cycle proteins are mainly expressed by dividing cells. However, it is well established that these molecules play additional non-canonical activities in several cell death contexts. Increasing evidence shows expression of cell cycle regulating proteins in post-mitotic cells, including mature neurons, following neuronal insult. Several cyclin-dependent kinases (Cdks) have already been shown to mediate ischemic neuronal death but Cdk1, a major cell cycle G2/M regulator, has not been investigated in this context. We therefore examined the role of Cdk1 in neuronal cell death following cerebral ischemia, using both in vitro and in vivo genetic and pharmacological approaches. Exposure of primary cortical neurons cultures to 4 h of oxygen-glucose deprivation (OGD) resulted in neuronal cell death and induced Cdk1 expression. Neurons from Cdk1-cKO mice showed partial resistance to OGD-induced neuronal cell death. Addition of R-roscovitine to the culture medium conferred neuroprotection against OGD-induced neuronal death. Transient 1-h occlusion of the cerebral artery (MCAO) also leads to Cdk1 expression and activation. Cdk1-cKO mice displayed partial resistance to transient 1-h MCAO. Moreover, systemic delivery of R-roscovitine was neuroprotective following transient 1-h MCAO. This study demonstrates that promising neuroprotective therapies can be considered through inhibition of the cell cycle machinery and particularly through pharmacological inhibition of Cdk1.

Identifiers

PMID29581894
PMCPMC5856839
OpenAlexW2796305262

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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.