Evidence map›Paper›PMID 36168065›Full record

ReviewNature reviews. Molecular cell biology2023

Organization, dynamics and mechanoregulation of integrin-mediated cell-ECM adhesions.

Pakorn Kanchanawong, David A Calderwood

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 331 papers.

0numbers the graph read from it
0cells of the map it votes in
331citing papers in PubMed
61.3field-weighted citation impact, top 1% 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

331 citing papers in PubMed, 489 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Mechanical forces stimulate Golgi export.The Journal of cell biology · 2026
    Article
  8. Review
  9. Mechanical regulation of cell memory.Nature structural & molecular biology · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

271 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 at 2 institutions in 2 countries.

Pakorn KanchanawongMechanobiology Institute, National University of Singapore, Singapore, Singapore. biekp@nus.edu.sg.
David A CalderwoodDepartment of Pharmacology, Yale University School of Medicine, New Haven, CT, USA. david.calderwood@yale.edu.ORCID 0000-0002-0791-4142
National University of Singapore · SGYale University · US

Funding

Integrin Trafficking to Focal AdhesionsR01GM134148 · NIGMS · YALE UNIVERSITY · PI CALDERWOOD, DAVID A, TOOMRE, DEREK K. · 2020 to 2023
$1.8M
P21-activated kinases in cell-cell and cell-matrix adhesion signalingR01GM138411 · NIGMS · YALE UNIVERSITY · PI BOGGON, TITUS JONATHON, CALDERWOOD, DAVID A · 2020 to 2023
$1.7M
NIGMS NIH HHS R01 GM134148NIGMS NIH HHS R01 GM138411
6 · The paper itself

Abstract

The ability of animal cells to sense, adhere to and remodel their local extracellular matrix (ECM) is central to control of cell shape, mechanical responsiveness, motility and signalling, and hence to development, tissue formation, wound healing and the immune response. Cell-ECM interactions occur at various specialized, multi-protein adhesion complexes that serve to physically link the ECM to the cytoskeleton and the intracellular signalling apparatus. This occurs predominantly via clustered transmembrane receptors of the integrin family. Here we review how the interplay of mechanical forces, biochemical signalling and molecular self-organization determines the composition, organization, mechanosensitivity and dynamics of these adhesions. Progress in the identification of core multi-protein modules within the adhesions and characterization of rearrangements of their components in response to force, together with advanced imaging approaches, has improved understanding of adhesion maturation and turnover and the relationships between adhesion structures and functions. Perturbations of adhesion contribute to a broad range of diseases and to age-related dysfunction, thus an improved understanding of their molecular nature may facilitate therapeutic intervention in these conditions.

Indexed as

Cell AdhesionCytoskeletonExtracellular MatrixIntegrinsAnimalsFocal AdhesionsSignal TransductionTissue AdhesionsIntegrins

Identifiers

PMID36168065
PMCPMC9892292
OpenAlexW4297383968

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.