Evidence map›Paper›PMID 21686264›Full record

ArticleSmall GTPases2010

Integrating chemotaxis and contact-inhibition during collective cell migration: Small GTPases at work.

Eric Theveneau, Roberto Mayor

Open access · hybridAbstract read
In one paragraph

Article in Small GTPases, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Microtubules: Evolving roles and critical cellular interactions.Experimental biology and medicine (Maywood, N.J.) · 2019
    Review
  7. Article
  8. Article
  9. Mechanisms of Cell Polarization.Current opinion in systems biology · 2017
    Article
  10. Article
  11. Molecular basis of contact inhibition of locomotion.Cellular and molecular life sciences : CMLS · 2016
    Review
  12. Signaling filopodia in vertebrate embryonic development.Cellular and molecular life sciences : CMLS · 2016
    Review
  13. The front and rear of collective cell migration.Nature reviews. Molecular cell biology · 2016
    Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Small Rho GTPases in the control of cell shape and mobility.Cellular and molecular life sciences : CMLS · 2014
    Review
  20. 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

2 authors at 1 institution in 1 country.

Eric TheveneauDepartment of Cell and Developmental Biology; University College London; London UK.
Roberto Mayor
University College London · GB

Funding

Medical Research Council G0801145
6 · The paper itself

Abstract

For directional cell migration to occur cells must interpret guiding cues present in their environment. Chemotaxis based on negative or positive signals has been long thought as the main driving force of guided cell migration. However during collective cell migration cells do receive information from external signals but also upon interactions with their direct neighbours. These multiple inputs must be translated into intracellular reorganisation in order to promote efficient directional migration. Small GTPases, being involved in establishing cell polarity and regulating protrusive activity, are likely to play a central role in signal integration. Indeed, recent findings from our laboratory indicate that Contact-Inhibition of Locomotion controlled by N-Cadherin and chemotaxis dependent on Sdf1/Cxcr4 signaling converge towards regulation of the localized activity of RhoA and Rac1. All together they establish cell polarity and select well-oriented cell protrusions to ensure directional cell migration.

Identifiers

PMID21686264
PMCPMC3116595
OpenAlexW2086571440

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.