Evidence map›Paper›PMID 38591541›Full record

ArticleeLife2024

N-cadherin directs the collective Schwann cell migration required for nerve regeneration through Slit2/3-mediated contact inhibition of locomotion.

Julian J A Hoving, Elizabeth Harford-Wright, Patrick Wingfield-Digby, Anne-Laure Cattin, Mariana Campana, Alex Power, Toby Morgan, Erica Torchiaro, Victor Quereda, Alison C Lloyd

Open access · goldAbstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

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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

10 authors at 1 institution in 2 countries.

Julian J A Hoving *UCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Elizabeth Harford-Wright *UCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-7231-2108
Patrick Wingfield-DigbyUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Anne-Laure CattinUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Mariana CampanaUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Alex PowerUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Toby MorganUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Erica TorchiaroUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Victor QueredaUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.
Alison C LloydUCL Laboratory for Molecular Cell Biology and the UCL Cancer Institute, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-7712-1773
Cancer Institute (WIA) · IN

Funding

Cancer Research UK C378/A4308Medical Research Council Studentship
6 · The paper itself

Abstract

Collective cell migration is fundamental for the development of organisms and in the adult for tissue regeneration and in pathological conditions such as cancer. Migration as a coherent group requires the maintenance of cell-cell interactions, while contact inhibition of locomotion (CIL), a local repulsive force, can propel the group forward. Here we show that the cell-cell interaction molecule, N-cadherin, regulates both adhesion and repulsion processes during Schwann cell (SC) collective migration, which is required for peripheral nerve regeneration. However, distinct from its role in cell-cell adhesion, the repulsion process is independent of N-cadherin

Indexed as

CadherinsCell MovementContact InhibitionIntercellular Signaling Peptides and ProteinsMembrane ProteinsNerve RegenerationNerve Tissue ProteinsSchwann CellsAnimalsCell AdhesionLocomotionMiceSignal TransductionSlit Homolog 2 ProteinCadherinsIntercellular Signaling Peptides and ProteinsMembrane ProteinsNerve Tissue ProteinsSlit3 protein, mouseSlit Homolog 2 Proteincancercancer biologycell biologycell–cell interactionscollective cell migrationcontact inhibition of locomotionmouseN-cadherinnerve regnerationratSchwann cellsSlit-Robo signalling

Identifiers

PMID38591541
PMCPMC11052573
OpenAlexW4394610273

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.