Evidence map›Paper›PMID 29555900›Full record

ArticleNature communications2018

Glycogen synthase kinase 3 controls migration of the neural crest lineage in mouse and Xenopus.

Sandra G Gonzalez Malagon, Anna M Lopez Muñoz, Daniel Doro, Triòna G Bolger, Evon Poon, Elizabeth R Tucker, Hadeel Adel Al-Lami, Matthias Krause, Christopher J Phiel, Louis Chesler and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.3field-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

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  7. The Tumor SuppressorJournal of developmental biology · 2023
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  15. Article
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  17. A genome-scale CRISPR screen reveals factors regulating Wnt-dependent renewal of mouse gastric epithelial cells.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Article
  19. Review
  20. LIN28B regulates transcription and potentiates MYCN-induced neuroblastoma through binding to ZNF143 at target gene promotors.Proceedings of the National Academy of Sciences of the United States of America · 2020
    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

11 authors at 3 institutions in 2 countries.

Sandra G Gonzalez MalagonCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Anna M Lopez MuñozCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Daniel DoroCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Triòna G BolgerCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Evon PoonPaediatric Solid Tumour Biology, Institute of Cancer Research/Royal Marsden NHS Trust, Surrey, SM2 5NG, UK.
Elizabeth R TuckerPaediatric Solid Tumour Biology, Institute of Cancer Research/Royal Marsden NHS Trust, Surrey, SM2 5NG, UK.
Hadeel Adel Al-LamiCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK.
Matthias KrauseRandall Division of Cell & Molecular Biophysics, King's College London, London, SE1 1UL, UK.
Christopher J PhielDepartment of Integrative Biology, University of Colorado Denver, Denver, CO, 80204, USA.
Louis CheslerPaediatric Solid Tumour Biology, Institute of Cancer Research/Royal Marsden NHS Trust, Surrey, SM2 5NG, UK.ORCID http://orcid.org/0000-0001-7842-2068
Karen J LiuCentre for Craniofacial and Regenerative Biology, King's College London, London, SE1 9RT, UK. karen.liu@kcl.ac.uk.ORCID http://orcid.org/0000-0002-2483-2165
King's College London · GBInstitute of Cancer Research · GBUniversity of Colorado Denver · US

Funding

Biotechnology and Biological Sciences Research Council BB/E013872/1Biotechnology and Biological Sciences Research Council BB/N000226/1Biotechnology and Biological Sciences Research Council BB/R015953/1Wellcome Trust
6 · The paper itself

Abstract

Neural crest migration is critical to its physiological function. Mechanisms controlling mammalian neural crest migration are comparatively unknown, due to difficulties accessing this cell population in vivo. Here we report requirements of glycogen synthase kinase 3 (GSK3) in regulating the neural crest in Xenopus and mouse models. We demonstrate that GSK3 is tyrosine phosphorylated (pY) in mouse neural crest cells and that loss of GSK3 leads to increased pFAK and misregulation of Rac1 and lamellipodin, key regulators of cell migration. Genetic reduction of GSK3 results in failure of migration. We find that pY-GSK3 phosphorylation depends on anaplastic lymphoma kinase (ALK), a protein associated with neuroblastoma. Consistent with this, neuroblastoma cells with increased ALK activity express high levels of pY-GSK3, and blockade of GSK3 or ALK can affect migration of these cells. Altogether, this work identifies a role for GSK3 in cell migration during neural crest development and cancer.

Indexed as

Anaplastic Lymphoma KinaseAnimalsCell LineageCell Line, TumorCell MovementFemaleGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaHumansMiceMice, KnockoutNeural CrestNeuroblastomaPhosphorylationPregnancyXenopus laevisAnaplastic Lymphoma KinaseGlycogen Synthase Kinase 3glycogen synthase kinase 3 alphaGlycogen Synthase Kinase 3 betaGsk3b protein, mouseGSK3B protein, XenopusXenopus Proteins

Identifiers

PMID29555900
PMCPMC5859133
OpenAlexW2791386712

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.