Evidence map›Paper›PMID 34999131›Full record

ArticleBiophysical journal2022

Cell monolayer deformation microscopy reveals mechanical fragility of cell monolayers following EMT.

Amy A Sutton, Clayton W Molter, Ali Amini, Johanan Idicula, Max Furman, Pouria Tirgar, Yuanyuan Tao, Ajinkya Ghagre, Newsha Koushki, Adele Khavari and 1 more

Open access · greenAbstract read
In one paragraph

Article in Biophysical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

11 authors at 1 institution in 1 country.

Amy A SuttonDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Clayton W MolterDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Ali AminiDepartment of Mechanical Engineering, McGill University, Montreal, Quebec, Canada.
Johanan IdiculaDepartment of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.
Max FurmanDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Pouria TirgarDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Yuanyuan TaoDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Ajinkya GhagreDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Newsha KoushkiDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Adele KhavariDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada.
Allen J EhrlicherDepartment of Bioengineering, McGill University, Montreal, Quebec, Canada; Department of Mechanical Engineering, McGill University, Montreal, Quebec, Canada; Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada; Department of Biomedical Engineering, McGill University, Montreal, Quebec, Canada; Centre for Structural Biology, McGill University, Montreal, Quebec, Canada; Goodman Cancer Research Centre, McGill University, Montreal, Quebec, Canada. Electronic address: allen.ehrlicher@mcgill.ca.
McGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissue and cell mechanics are crucial factors in maintaining homeostasis and in development, with aberrant mechanics contributing to many diseases. During the epithelial-to-mesenchymal transition (EMT), a highly conserved cellular program in organismal development and cancer metastasis, cells gain the ability to detach from their original location and autonomously migrate. While a great deal of biochemical and biophysical changes at the single-cell level have been revealed, how the physical properties of multicellular assemblies change during EMT, and how this may affect disease progression, is unknown. Here we introduce cell monolayer deformation microscopy (CMDM), a new methodology to measure the planar mechanical properties of cell monolayers by locally applying strain and measuring their resistance to deformation. We employ this new method to characterize epithelial multicellular mechanics at early and late stages of EMT, finding the epithelial monolayers to be relatively compliant, ductile, and mechanically homogeneous. By comparison, the transformed mesenchymal monolayers, while much stiffer, were also more brittle, mechanically heterogeneous, displayed more viscoelastic creep, and showed sharp yield points at significantly lower strains. Here, CMDM measurements identify specific biophysical functional states of EMT and offer insight into how cell aggregates fragment under mechanical stress. This mechanical fingerprinting of multicellular assemblies using new quantitative metrics may also offer new diagnostic applications in healthcare to characterize multicellular mechanical changes in disease.

Indexed as

Epithelial-Mesenchymal TransitionMicroscopyStress, Mechanical

Identifiers

PMID34999131
PMCPMC8873957
OpenAlexW4205439674

What OpenQuestion holds

Textmetadata
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.