Evidence map›Paper›PMID 37838732›Full record

ArticleCommunications biology2023

Aberrant MET activation impairs perinuclear actin cap organization with YAP1 cytosolic relocation.

Michela Sgarzi, Martina Mazzeschi, Spartaco Santi, Elisa Montacci, Tito Panciera, Enea Ferlizza, Cinzia Girone, Alessandra Morselli, Valerio Gelfo, Rikke Sofie Kuhre and 7 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Metastatic organotropism in small cell lung cancer.bioRxiv : the preprint server for biology · 2025
    Article
  5. Review
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

17 authors at 6 institutions in 2 countries.

Michela Sgarzi *IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0003-0949-7810
Martina Mazzeschi *IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Spartaco SantiInstitute of Molecular Genetics, National Research Council of Italy, Bologna, Italy.ORCID http://orcid.org/0000-0001-9856-7053
Elisa MontacciDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Tito PancieraDepartment of Molecular Medicine, University of Padua, Padua, Italy.
Enea FerlizzaDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0003-3391-0679
Cinzia GironeDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Alessandra MorselliDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Valerio GelfoDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Rikke Sofie KuhreDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID http://orcid.org/0009-0000-3419-1085
Carola CavalloLaboratory of Preclinical Studies for Regenerative Medicine of the Musculoskeletal System (RAMSES), (IRCCS) Istituto Ortopedico Rizzoli, Bologna, Italy.ORCID http://orcid.org/0000-0002-2913-856X
Sabrina ValenteDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Gianandrea PasquinelliDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Balazs GyőrffySemmelweis University Dept. of Bioinformatics and 2nd Dept. Of Pediatrics, Budapest, Hungary.
Gabriele D'UvaDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
Donatella RomanielloDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy. donatella.romaniello@unibo.it.ORCID http://orcid.org/0000-0001-8278-1637
Mattia LauriolaDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy. mattia.lauriola2@unibo.it.ORCID http://orcid.org/0000-0002-7966-0065
University of Bologna · ITAzienda USL di Bologna · ITIstituto Ortopedico Rizzoli · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITSemmelweis University · HUUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little is known about the signaling network responsible for the organization of the perinuclear actin cap, a recently identified structure holding unique roles in the regulation of nuclear shape and cell directionality. In cancer cells expressing a constitutively active MET, we show a rearrangement of the actin cap filaments, which crash into perinuclear patches associated with spherical nuclei, meandering cell motility and inactivation of the mechano-transducer YAP1. MET ablation is sufficient to reactivate YAP1 and restore the cap, leading to enhanced directionality and flattened nuclei. Consistently, the introduction of a hyperactive MET in normal epithelial cells, enhances nuclear height and alters the cap organization, as also confirmed by TEM analysis. Finally, the constitutively active YAP1 mutant YAP5SA is able to overcome the effects of oncogenic MET. Overall, our work describes a signaling axis empowering MET-mediated YAP1 dampening and actin cap misalignment, with implications for nuclear shape and cell motility.

Indexed as

Actin CytoskeletonActinsCell MovementCell NucleusCytosolActins

Identifiers

PMID37838732
PMCPMC10576810
OpenAlexW4387640013

What Socratic 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 Socratic graph.