Evidence map›Paper›PMID 33924599›Full record

ArticleInternational journal of molecular sciences2021

DYRK1A Negatively Regulates CDK5-SOX2 Pathway and Self-Renewal of Glioblastoma Stem Cells.

Brianna Chen, Dylan McCuaig-Walton, Sean Tan, Andrew P Montgomery, Bryan W Day, Michael Kassiou, Lenka Munoz, Ariadna Recasens

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Cancer stem cell fate determination: mito-nuclear communication.Cell communication and signaling : CCS · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. The role of Cdk5 in neurological disorders.Frontiers in cellular neuroscience · 2022
    Review
  13. 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

8 authors at 2 institutions in 1 country.

Brianna ChenCharles Perkins Centre and School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.
Dylan McCuaig-WaltonCharles Perkins Centre and School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.
Sean TanCharles Perkins Centre and School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.
Andrew P MontgomerySchool of Chemistry, Faculty of Science, The University of Sydney, Sydney, NSW 2006, Australia.ORCID 0000-0002-1819-3619
Bryan W DayQIMR Berghofer Medical Research Institute, 300 Herston Road, Herston, QLD 4006, Australia.
Michael KassiouSchool of Chemistry, Faculty of Science, The University of Sydney, Sydney, NSW 2006, Australia.
Lenka MunozCharles Perkins Centre and School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.
Ariadna RecasensCharles Perkins Centre and School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW 2006, Australia.ORCID 0000-0002-0564-4150
The University of Sydney · AUQIMR Berghofer Medical Research Institute · AU

Funding

Cancer Institute NSW 15/CDF/1-07National Health and Medical Research Council APP1106145
6 · The paper itself

Abstract

Glioblastoma display vast cellular heterogeneity, with glioblastoma stem cells (GSCs) at the apex. The critical role of GSCs in tumour growth and resistance to therapy highlights the need to delineate mechanisms that control stemness and differentiation potential of GSC. Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) regulates neural progenitor cell differentiation, but its role in cancer stem cell differentiation is largely unknown. Herein, we demonstrate that DYRK1A kinase is crucial for the differentiation commitment of glioblastoma stem cells. DYRK1A inhibition insulates the self-renewing population of GSCs from potent differentiation-inducing signals. Mechanistically, we show that DYRK1A promotes differentiation and limits stemness acquisition via deactivation of CDK5, an unconventional kinase recently described as an oncogene. DYRK1A-dependent inactivation of CDK5 results in decreased expression of the stemness gene SOX2 and promotes the commitment of GSC to differentiate. Our investigations of the novel DYRK1A-CDK5-SOX2 pathway provide further insights into the mechanisms underlying glioblastoma stem cell maintenance.

Indexed as

Cell Self RenewalBone Morphogenetic Protein 4Cell DifferentiationCyclin-Dependent Kinase 5Dyrk KinasesGene Expression Regulation, NeoplasticGlioblastomaHumansNeoplastic Stem CellsProtein Serine-Threonine KinasesProtein-Tyrosine KinasesSignal TransductionSOXB1 Transcription FactorsBone Morphogenetic Protein 4CDK5 protein, humanCyclin-Dependent Kinase 5Dyrk KinasesProtein Serine-Threonine KinasesProtein-Tyrosine KinasesSOX2 protein, humanSOXB1 Transcription Factorsbone morphogenetic protein 4 (BMP4)cancer stem cellsCDK5DYRK1AglioblastomaSOX2

Identifiers

PMID33924599
PMCPMC8069695
OpenAlexW3156519105

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.