Evidence map›Paper›PMID 38575601›Full record

ArticleCell death & disease2024

Genetic and pharmacological reduction of CDK14 mitigates synucleinopathy.

Jean-Louis A Parmasad, Konrad M Ricke, Benjamin Nguyen, Morgan G Stykel, Brodie Buchner-Duby, Amanda Bruce, Haley M Geertsma, Eric Lian, Nathalie A Lengacher, Steve M Callaghan and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

18 authors at 4 institutions in 3 countries.

Jean-Louis A Parmasad *University of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.ORCID 0000-0001-5013-2317
Konrad M Ricke *University of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.
Benjamin NguyenUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.
Morgan G StykelDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.
Brodie Buchner-DubyDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.
Amanda BruceUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.
Haley M GeertsmaUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.
Eric LianDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
Nathalie A LengacherUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.ORCID 0000-0002-2536-1895
Steve M CallaghanUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.ORCID 0000-0001-6692-4060
Alvin JoselinHotchkiss Brain Institute, Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-9010-0421
Julianna J TomlinsonUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.
Michael G SchlossmacherUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada.
William L StanfordDepartment of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.ORCID 0000-0002-5813-8016
Jiyan MaParkinson's Disease Center, Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.ORCID 0000-0001-7150-1898
Patrik BrundinParkinson's Disease Center, Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA.ORCID 0000-0003-2924-5186
Scott D RyanDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, ON, Canada.ORCID 0000-0001-9829-4649
Maxime W C RousseauxUniversity of Ottawa Brain and Mind Research Institute, Ottawa, ON, Canada. max.rousseaux@uottawa.ca.ORCID 0000-0002-2737-6193
University of Ottawa · CAUniversity of Guelph · CAVan Andel Institute · USUniversity of Calgary · CA

Funding

Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) CIHR CGS-DGouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) FRN-153188Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) FRN-159443Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) PJT-169097Michael J. Fox Foundation for Parkinson's Research (Michael J. Fox Foundation) ASAP-020625Parkinson Canada 2018-00016Parkinson Canada BRF-2021-0000000048
6 · The paper itself

Abstract

Parkinson's disease (PD) is a debilitating neurodegenerative disease characterized by the loss of midbrain dopaminergic neurons (DaNs) and the abnormal accumulation of α-Synuclein (α-Syn) protein. Currently, no treatment can slow nor halt the progression of PD. Multiplications and mutations of the α-Syn gene (SNCA) cause PD-associated syndromes and animal models that overexpress α-Syn replicate several features of PD. Decreasing total α-Syn levels, therefore, is an attractive approach to slow down neurodegeneration in patients with synucleinopathy. We previously performed a genetic screen for modifiers of α-Syn levels and identified CDK14, a kinase of largely unknown function as a regulator of α-Syn. To test the potential therapeutic effects of CDK14 reduction in PD, we ablated Cdk14 in the α-Syn preformed fibrils (PFF)-induced PD mouse model. We found that loss of Cdk14 mitigates the grip strength deficit of PFF-treated mice and ameliorates PFF-induced cortical α-Syn pathology, indicated by reduced numbers of pS129 α-Syn-containing cells. In primary neurons, we found that Cdk14 depletion protects against the propagation of toxic α-Syn species. We further validated these findings on pS129 α-Syn levels in PD patient neurons. Finally, we leveraged the recent discovery of a covalent inhibitor of CDK14 to determine whether this target is pharmacologically tractable in vitro and in vivo. We found that CDK14 inhibition decreases total and pathologically aggregated α-Syn in human neurons, in PFF-challenged rat neurons and in the brains of α-Syn-humanized mice. In summary, we suggest that CDK14 represents a novel therapeutic target for PD-associated synucleinopathy.

Indexed as

Neurodegenerative DiseasesParkinson DiseaseSynucleinopathiesalpha-SynucleinAnimalsCyclin-Dependent KinasesDopaminergic NeuronsHumansMesencephalonMiceRatsalpha-SynucleinCDK14 protein, humanCdk14 protein, ratCyclin-Dependent Kinases

Identifiers

PMID38575601
PMCPMC10994937
OpenAlexW4393941511

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.