Evidence map›Paper›PMID 30554899›Full record

ArticleCurrent biology : CB2019

Competition for Space Induces Cell Elimination through Compaction-Driven ERK Downregulation.

Eduardo Moreno, Léo Valon, Florence Levillayer, Romain Levayer

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 143 citations in OpenAlex.

  1. Mechanics of compression-driven morphogenesis.Development (Cambridge, England) · 2026
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  9. Tissue turnover and rejuvenation through mechanics.Frontiers in cell and developmental biology · 2026
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  19. bioRxiv : the preprint server for biology · 2025
    Article
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21 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

4 authors at 3 institutions in 2 countries.

Eduardo MorenoChampalimaud Centre for the Unknown, Av. Brasília, 1400-038 Lisbon, Portugal. Electronic address: eduardo.moreno@research.fchampalimaud.org.
Léo ValonDepartment of Developmental and Stem Cell Biology, Institut Pasteur, 25 rue du Dr. Roux, 75015 Paris, France.
Florence LevillayerDepartment of Developmental and Stem Cell Biology, Institut Pasteur, 25 rue du Dr. Roux, 75015 Paris, France.
Romain LevayerDepartment of Developmental and Stem Cell Biology, Institut Pasteur, 25 rue du Dr. Roux, 75015 Paris, France. Electronic address: romain.levayer@pasteur.fr.
Biologie du Développement et Cellules SouchesChampalimaud Foundation · PTLaboratoire de Biologie du Développement · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The plasticity of developing tissues relies on the adjustment of cell survival and growth rate to environmental cues. This includes the effect of mechanical cues on cell survival. Accordingly, compaction of an epithelium can lead to cell extrusion and cell death. This process was proposed to contribute to tissue homeostasis but also to facilitate the expansion of pretumoral cells through the compaction and elimination of the neighboring healthy cells. However, we know very little about the pathways that can trigger apoptosis upon tissue deformation, and the contribution of compaction-driven death to clone expansion has never been assessed in vivo. Using the Drosophila pupal notum and a new live sensor of ERK, we show first that tissue compaction induces cell elimination through the downregulation of epidermal growth factor receptor/extracellular signal regulated kinase (EGFR/ERK) pathway and the upregulation of the pro-apoptotic protein Hid. Those results suggest that the sensitivity of EGFR/ERK pathway to mechanics could play a more general role in the fine tuning of cell elimination during morphogenesis and tissue homeostasis. Second, we assessed in vivo the contribution of compaction-driven death to pretumoral cell expansion. We found that the activation of the oncogene Ras in clones can downregulate ERK and activate apoptosis in the neighboring cells through their compaction, which eventually contributes to Ras clone expansion. The mechanical modulation of EGFR/ERK during growth-mediated competition for space may contribute to tumor progression.

Indexed as

Down-RegulationSignal TransductionAnimalsCell SizeCell SurvivalDrosophila melanogasterDrosophila ProteinsErbB ReceptorsExtracellular Signal-Regulated MAP KinasesPupaDrosophila ProteinsErbB ReceptorsExtracellular Signal-Regulated MAP Kinasesapoptosiscell competitionDrosophilaEGFRepitheliumERKHidmechanotransduction

Identifiers

PMID30554899
PMCPMC6331351
OpenAlexW2949896630

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.