Evidence map›Paper›PMID 26726037›Full record

ReviewNature reviews. Molecular cell biology2016

The front and rear of collective cell migration.

Roberto Mayor, Sandrine Etienne-Manneville

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Molecular cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 427 papers.

0numbers the graph read from it
0cells of the map it votes in
427citing papers in PubMed
–field-weighted citation impact
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

427 citing papers in PubMed.

  1. Trial
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  3. Cell jamming transition is regulated by mitochondrial pyruvate transport and endocytosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
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367 more citing papers are in PubMed but not listed here.

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

2 authors.

Roberto MayorDepartment of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, UK.
Sandrine Etienne-MannevilleInstitut Pasteur, CNRS UMR 3691, Cell Polarity, Migration and Cancer Unit, 25 Rue du Dr Roux, 75724 Paris Cedex 15, France.

Funding

Biotechnology and Biological Sciences Research Council M008517Medical Research Council J000655Medical Research Council M010465Medical Research Council MR/M010465/1
6 · The paper itself

Abstract

Collective cell migration has a key role during morphogenesis and during wound healing and tissue renewal in the adult, and it is involved in cancer spreading. In addition to displaying a coordinated migratory behaviour, collectively migrating cells move more efficiently than if they migrated separately, which indicates that a cellular interplay occurs during collective cell migration. In recent years, evidence has accumulated confirming the importance of such intercellular communication and exploring the molecular mechanisms involved. These mechanisms are based both on direct physical interactions, which coordinate the cellular responses, and on the collective cell behaviour that generates an optimal environment for efficient directed migration. The recent studies have described how leader cells at the front of cell groups drive migration and have highlighted the importance of follower cells and cell-cell communication, both between followers and between follower and leader cells, to improve the efficiency of collective movement.

Indexed as

Cell CommunicationCell MovementActin CytoskeletonAdherens JunctionsAnimalsCell PolarityExtracellular Matrix ProteinsGene Expression RegulationHumansMorphogenesisNeoplasm Invasivenessrac1 GTP-Binding ProteinSignal TransductionWound HealingExtracellular Matrix Proteinsrac1 GTP-Binding Protein

Identifiers

PMID26726037

What OpenQuestion holds

Textmetadata
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.