Evidence map›Paper›PMID 35482006›Full record

ArticleThe Journal of cell biology2022

Interphase microtubule disassembly is a signaling cue that drives cell rounding at mitotic entry.

Kévin Leguay, Barbara Decelle, Islam E Elkholi, Michel Bouvier, Jean-François Côté, Sébastien Carréno

Open access · greenAbstract read
In one paragraph

Article in The Journal of cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Osmotic Pressure and Its Biological Implications.International journal of molecular sciences · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Hypoxia enhances interactions between NaFrontiers in physiology · 2023
    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

6 authors at 2 institutions in 1 country.

Kévin LeguayInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.ORCID 0000-0002-5691-4157
Barbara DecelleInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.
Islam E ElkholiMontréal Clinical Research Institute, Montréal, Quebec, Canada.ORCID 0000-0002-8019-2481
Michel BouvierInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.ORCID 0000-0003-1128-0100
Jean-François CôtéMontréal Clinical Research Institute, Montréal, Quebec, Canada.ORCID 0000-0001-7055-2642
Sébastien CarrénoInstitute for Research in Immunology and Cancer, Université de Montréal, Montréal, Quebec, Canada.ORCID 0000-0002-5839-2102
Institute for Research in Immunology and Cancer · CAMontreal Clinical Research Institute · CA

Funding

Canada Research ChairCanadian Cancer Society Research Institute 705892CIHR 175193Fonds de Recherche du Québec - SantéInstitute for Research in Immunology and CancerMontréal UniversityNational Science and Engineering Research Council of Canada RGPIN-201604808Transat Chair in Breast Cancer Research
6 · The paper itself

Abstract

At mitotic entry, reorganization of the actomyosin cortex prompts cells to round-up. Proteins of the ezrin, radixin, and moesin family (ERM) play essential roles in this process by linking actomyosin forces to the plasma membrane. Yet, the cell-cycle signal that activates ERMs at mitotic entry is unknown. By screening a compound library using newly developed biosensors, we discovered that drugs that disassemble microtubules promote ERM activation. We further demonstrated that disassembly of interphase microtubules at mitotic entry directs ERM activation and metaphase cell rounding through GEF-H1, a Rho-GEF inhibited by microtubule binding, RhoA, and its kinase effector SLK. We finally demonstrated that GEF-H1 and Ect2, another Rho-GEF previously identified to control actomyosin forces, act together to drive activation of ERMs and cell rounding in metaphase. In summary, we report microtubule disassembly as a cell-cycle signal that controls a signaling network ensuring that actomyosin forces are efficiently integrated at the plasma membrane to promote cell rounding at mitotic entry.

Indexed as

ActomyosinInterphaseMicrotubulesRho Guanine Nucleotide Exchange FactorsCell ShapeHEK293 CellsHumansMitosisProto-Oncogene ProteinsActomyosinARHGEF2 protein, humanECT2 protein, humanProto-Oncogene ProteinsRho Guanine Nucleotide Exchange Factors

Identifiers

PMID35482006
PMCPMC9059391
OpenAlexW4225311788

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.