Evidence map›Paper›PMID 38984538›Full record

ArticleCytoskeleton (Hoboken, N.J.)2025

A truncation mutant of adenomatous polyposis coli impairs apical cell extrusion through elevated epithelial tissue tension.

Wan J Gan, Rabina Giri, Jakob Begun, Helen E Abud, Edna C Hardeman, Peter W Gunning, Alpha S Yap, Ivar Noordstra

Abstract read
In one paragraph

Article in Cytoskeleton (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

8 authors.

Wan J GanCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland, Australia.
Rabina GiriMater Research Institute, The University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
Jakob BegunMater Research Institute, The University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
Helen E AbudDepartment of Anatomy and Developmental Biology, Development and Stem Cells Program, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Edna C HardemanFaculty of Medicine and Health, School of Biomedical Sciences, University of New South Wales, Sydney, New South Wales, Australia.
Peter W GunningFaculty of Medicine and Health, School of Biomedical Sciences, University of New South Wales, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0003-0833-3128
Alpha S YapCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland, Australia.
Ivar NoordstraCentre for Cell Biology of Chronic Disease, Institute for Molecular Bioscience, The University of Queensland, St Lucia, Queensland, Australia.ORCID https://orcid.org/0000-0001-5381-8795

Funding

Australian Research Council (ARC) DP220103951Australian Research Council (ARC) FL2023000092Department of Industry, Science and Resources CRC-P-355European Molecular Biology Organization (EMBO) ALTF 251-2018National Health and Medical Research Council (NHMRC) 1079866National Health and Medical Research Council (NHMRC) 1100202National Health and Medical Research Council (NHMRC) 2021181National Health and Medical Research Council (NHMRC) GNT2010704
6 · The paper itself

Abstract

Tissue tension encompasses the mechanical forces exerted on solid tissues within animal bodies, originating from various sources such as cellular contractility, interactions with neighboring cells and the extracellular matrix. Emerging evidence indicates that an imbalance in such forces can influence structural organization, homeostasis, and potentially contribute to disease. For instance, heightened tissue tension can impede apical cell extrusion, leading to the retention of apoptotic or transformed cells. In this study, we investigate the potential role of adenomatous polyposis coli (APC) in modulating tissue tension. Our findings reveal that expression of an APC truncation mutant elevates epithelial tension via the RhoA/ROCK pathway. This elevation induces morphological alterations and hampers apoptotic cell extrusion in cultured epithelial cells and organoids, both of which could be mitigated by pharmacologically restoring the tissue tension. This raises the possibility that APC mutations may exert pathogenetic effects by altering tissue mechanics.

Indexed as

Adenomatous Polyposis ColiAdenomatous Polyposis Coli ProteinEpithelial CellsMutationAnimalsApoptosisHumansAdenomatous Polyposis Coli Proteinactin cytoskeletonadherens junctionAPCapoptotic extrusiontissue tension

Identifiers

PMID38984538
PMCPMC12247696

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Registered trials

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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.