Evidence map›Paper›PMID 40988584›Full record

ArticleJournal of cell science2025

The integrin odyssey - a journey full of fundamental discoveries.

Reinhard Fässler, Arnoud Sonnenberg

Abstract read
In one paragraph

Article in Journal of cell science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Reinhard FässlerMax Planck Institute of Biochemistry, 82152 Martinsried, Germany.ORCID 0000-0002-0145-6937
Arnoud SonnenbergThe Netherlands Cancer Institute, Division of Cell Biology, 1066CX Amsterdam, The Netherlands.ORCID 0000-0001-9585-468X

Funding

Alexander von Humboldt-StiftungEuropean Research Council 810104 - PointMax Planck SocietyNetherlands Cancer Institute 30058
6 · The paper itself

Abstract

Integrins are widely expressed cell adhesion receptors that link extracellular matrix proteins to the cytoskeleton. Most integrins connect to the actin cytoskeleton through different types of adhesion plaques, including nascent adhesions and focal adhesions. They regulate adhesion strength in response to the mechanical force exerted by actomyosin across the plasma membrane. Beyond serving as mechanical connectors, integrins also play a crucial role in regulating cellular behaviour through biochemical signalling pathways. Given their essential functions, integrins are vital for the survival of metazoans and are important therapeutic targets for treating various human diseases. This Perspective highlights the work that led to the discovery of integrins and the principles of how they function.

Indexed as

IntegrinsActin CytoskeletonAnimalsCell AdhesionCytoskeletonFocal AdhesionsHumansSignal TransductionIntegrinsAdhesomeConformational transitionsFocal adhesionIntegrinSignalling

Identifiers

PMID40988584
PMCPMC12516132

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.