Evidence map›Paper›PMID 37342880›Full record

ArticleMolecular biology of the cell2023

Cell contractility drives mechanical memory of oral squamous cell carcinoma.

So Youn Moon, Paloma Santos de Campos, Bibiana Franzen Matte, Jesse K Placone, Virgı Lio G Zanella, Manoela D Martins, Marcelo Lazzaron Lamers, Adam J Engler

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.8field-weighted citation impact, top 5% 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, 23 citations in OpenAlex.

  1. Mechanical regulation of cell memory.Nature structural & molecular biology · 2026
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  12. Genetic variation drives cancer cell adaptation to ECM stiffness.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  17. Implications of Cellular Mechanical Memory in Bioengineering.ACS biomaterials science & engineering · 2023
    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

8 authors at 4 institutions in 2 countries.

So Youn MoonDepartment of Bioengineering, University of California San Diego, La Jolla, CA 92093.
Paloma Santos de CamposDepartment of Oral Pathology, Federal University of Rio Grande do Sul.
Bibiana Franzen MatteDepartment of Oral Pathology, Federal University of Rio Grande do Sul.
Jesse K PlaconeDepartment of Bioengineering, University of California San Diego, La Jolla, CA 92093.
Virgı Lio G ZanellaDepartment of Oral Pathology, Federal University of Rio Grande do Sul.
Manoela D MartinsDepartment of Oral Pathology, Federal University of Rio Grande do Sul.
Marcelo Lazzaron LamersDepartment of Oral Pathology, Federal University of Rio Grande do Sul.
Adam J EnglerDepartment of Bioengineering, University of California San Diego, La Jolla, CA 92093.
Universidade Federal do Rio Grande do Sul · BRSanford Consortium for Regenerative Medicine · USUniversity of California, San Diego · USUniversity of Rio Grande and Rio Grande Community College · US

Funding

Biomaterial Mimicry of Dynamic Matrix Stiffening During Tumor ProgressionR01CA206880 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ENGLER, ADAM J, YANG, JING · 2016 to 2020
$1.8M
Illumina NovaSeq 6000 Sequencing SystemS10OD026929 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEPSEN, KRISTEN LYNN · 2019 to 2019
$600k
NCI NIH HHS R01 CA206880NIH HHS S10 OD026929
6 · The paper itself

Abstract

Matrix stiffening is ubiquitous in solid tumors and can direct epithelial-mesenchymal transition (EMT) and cancer cell migration. Stiffened niche can even cause poorly invasive oral squamous cell carcinoma (OSCC) cell lines to acquire a less adherent, more migratory phenotype, but mechanisms and durability of this acquired "mechanical memory" are unclear. Here, we observed that contractility and its downstream signals could underlie memory acquisition; invasive SSC25 cells overexpress myosin II (vs. noninvasive Cal27 cells) consistent with OSCC. However, prolonged exposure of Cal27 cells to a stiff niche or contractile agonists up-regulated myosin and EMT markers and enabled them to migrate as fast as SCC25 cells, which persisted even when the niche softened and indicated "memory" of their prior niche. Stiffness-mediated mesenchymal phenotype acquisition required AKT signaling and was also observed in patient samples, whereas phenotype recall on soft substrates required focal adhesion kinase (FAK) activity. Phenotype durability was further observed in transcriptomic differences between preconditioned Cal27 cells cultured without or with FAK or AKT antagonists, and such transcriptional differences corresponded to discrepant patient outcomes. These data suggest that mechanical memory, mediated by contractility via distinct kinase signaling, may be necessary for OSCC to disseminate.

Indexed as

Carcinoma, Squamous CellHead and Neck NeoplasmsMouth NeoplasmsCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionHumansProto-Oncogene Proteins c-aktSquamous Cell Carcinoma of Head and NeckProto-Oncogene Proteins c-akt

Identifiers

PMID37342880
PMCPMC10398896
OpenAlexW4381490520

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.