Evidence map›Paper›PMID 34188099›Full record

ArticleScientific reports2021

Osmotic pressure modulates single cell cycle dynamics inducing reversible growth arrest and reactivation of human metastatic cells.

Hubert M Taïeb, Daniela S Garske, Jörg Contzen, Manfred Gossen, Luca Bertinetti, Tom Robinson, Amaia Cipitria

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
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  3. BPGM shapes NFAT5-driven cellular responses.Cellular and molecular life sciences : CMLS · 2026
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  4. Extracellular Matrix Viscoelasticity Regulates Mammary Branching Morphogenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  6. The Role of the Swollen State in Cell Proliferation.The Journal of membrane biology · 2025
    Review
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  11. Article
  12. Review
  13. Article
  14. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Hubert M TaïebDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14476, Potsdam, Germany.
Daniela S GarskeDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14476, Potsdam, Germany.
Jörg ContzenDepartment of Experimental Neurology, Charité-Universitätsmedizin Berlin, 10117, Berlin, Germany.
Manfred GossenInstitute of Active Polymers, Helmholtz-Zentrum Hereon, 14513, Teltow, Germany.
Luca BertinettiDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14476, Potsdam, Germany.
Tom RobinsonDepartment of Theory and Bio-Systems, Max Planck Institute of Colloids and Interfaces, 14476, Potsdam, Germany.
Amaia CipitriaDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14476, Potsdam, Germany. amaia.cipitria@mpikg.mpg.de.
Max Planck Institute of Colloids and Interfaces · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DEHelmholtz-Zentrum Hereon · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biophysical cues such as osmotic pressure modulate proliferation and growth arrest of bacteria, yeast cells and seeds. In tissues, osmotic regulation takes place through blood and lymphatic capillaries and, at a single cell level, water and osmoregulation play a critical role. However, the effect of osmotic pressure on single cell cycle dynamics remains poorly understood. Here, we investigate the effect of osmotic pressure on single cell cycle dynamics, nuclear growth, proliferation, migration and protein expression, by quantitative time-lapse imaging of single cells genetically modified with fluorescent ubiquitination-based cell cycle indicator 2 (FUCCI2). Single cell data reveals that under hyperosmotic stress, distinct cell subpopulations emerge with impaired nuclear growth, delayed or growth arrested cell cycle and reduced migration. This state is reversible for mild hyperosmotic stress, where cells return to regular cell cycle dynamics, proliferation and migration. Thus, osmotic pressure can modulate the reversible growth arrest and reactivation of human metastatic cells.

Indexed as

Cell DivisionOsmotic PressureUbiquitinationBreast NeoplasmsFemaleHumansMCF-7 CellsNeoplasm Metastasis

Identifiers

PMID34188099
PMCPMC8242012
OpenAlexW3174620687

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.