Evidence map›Paper›PMID 25418163›Full record

ArticleBiophysical journal2014

Compressive stress inhibits proliferation in tumor spheroids through a volume limitation.

Morgan Delarue, Fabien Montel, Danijela Vignjevic, Jacques Prost, Jean-François Joanny, Giovanni Cappello

Abstract read
In one paragraph

Article in Biophysical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 139 papers.

0numbers the graph read from it
0cells of the map it votes in
139citing 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

139 citing papers in PubMed.

  1. Article
  2. Mechanics of compression-driven morphogenesis.Development (Cambridge, England) · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Amoeboid-mesenchymal transition and the proteolytic control of cancer invasion plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Article
  10. Metabolic starvation-induced cell swelling drives solid stress in tumors.bioRxiv : the preprint server for biology · 2026
    Article
  11. Article
  12. Review
  13. The importance of mechanical forces in chronic respiratory diseases.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

79 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Morgan DelaruePhysicochimie Curie (Institut Curie/Centre National de la Recherche Scientifique-UMR168/Université Pierre et Marie Curie), Institut Curie, Centre de Recherche, Paris, France. Electronic address: morgan.delarue@berkeley.edu.
Fabien MontelMatière et Système Complexes (Université Paris-Diderot/Centre National de la Recherche Scientifique-UMR 7057), Paris, France.
Danijela VignjevicInstitut Curie/Centre National de la Recherche Scientifique-UMR144 /Université Pierre et Marie Curie, Institut Curie, Centre de Recherche, Paris, France.
Jacques ProstPhysicochimie Curie (Institut Curie/Centre National de la Recherche Scientifique-UMR168/Université Pierre et Marie Curie), Institut Curie, Centre de Recherche, Paris, France.
Jean-François JoannyPhysicochimie Curie (Institut Curie/Centre National de la Recherche Scientifique-UMR168/Université Pierre et Marie Curie), Institut Curie, Centre de Recherche, Paris, France.
Giovanni CappelloPhysicochimie Curie (Institut Curie/Centre National de la Recherche Scientifique-UMR168/Université Pierre et Marie Curie), Institut Curie, Centre de Recherche, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In most instances, the growth of solid tumors occurs in constrained environments and requires a competition for space. A mechanical crosstalk can arise from this competition. In this article, we dissect the biomechanical sequence caused by a controlled compressive stress on multicellular spheroids (MCSs) used as a tumor model system. On timescales of minutes, we show that a compressive stress causes a reduction of the MCS volume, linked to a reduction of the cell volume in the core of the MCS. On timescales of hours, we observe a reversible induction of the proliferation inhibitor, p27Kip1, from the center to the periphery of the spheroid. On timescales of days, we observe that cells are blocked in the cell cycle at the late G1 checkpoint, the restriction point. We show that the effect of pressure on the proliferation can be antagonized by silencing p27Kip1. Finally, we quantify a clear correlation between the pressure-induced volume change and the growth rate of the spheroid. The compression-induced proliferation arrest that we studied is conserved for five cell lines, and is completely reversible. It demonstrates a generic crosstalk between mechanical stresses and the key players of cell cycle regulation. Our results suggest a role of volume change in the sensitivity to pressure, and that p27Kip1 is strongly influenced by this change.

Indexed as

Cell ProliferationCell SizeCompressive StrengthAnimalsG1 Phase Cell Cycle CheckpointsHT29 CellsHumansMiceSpheroids, Cellular

Identifiers

PMID25418163
PMCPMC4213738

What OpenQuestion holds

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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.