Evidence map›Paper›PMID 30104699›Full record

ArticleScientific reports2018

Quantitative phase imaging unravels new insight into dynamics of mesenchymal and amoeboid cancer cell invasion.

Ondřej Tolde, Aneta Gandalovičová, Aneta Křížová, Pavel Veselý, Radim Chmelík, Daniel Rosel, Jan Brábek

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

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  11. Biomass measurements of single neuritesBiomedical optics express · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Cancer cell metabolic plasticity in migration and metastasis.Clinical & experimental metastasis · 2021
    Review
  17. Article
  18. Article
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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

7 authors.

Ondřej ToldeDepartment of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic.
Aneta GandalovičováDepartment of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic.
Aneta KřížováCentral European Institute of Technology, Brno University of Technology, Purkyňova 656/123, 612 00, Brno, Czech Republic.
Pavel VeselýCentral European Institute of Technology, Brno University of Technology, Purkyňova 656/123, 612 00, Brno, Czech Republic.
Radim ChmelíkCentral European Institute of Technology, Brno University of Technology, Purkyňova 656/123, 612 00, Brno, Czech Republic.ORCID 0000-0001-5410-4794
Daniel RoselDepartment of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic.
Jan BrábekDepartment of Cell Biology, Charles University, Viničná 7, Prague, Czech Republic. jan.brabek@natur.cuni.cz.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Observation and analysis of cancer cell behaviour in 3D environment is essential for full understanding of the mechanisms of cancer cell invasion. However, label-free imaging of live cells in 3D conditions is optically more challenging than in 2D. Quantitative phase imaging provided by coherence controlled holographic microscopy produces images with enhanced information compared to ordinary light microscopy and, due to inherent coherence gate effect, enables observation of live cancer cells' activity even in scattering milieu such as the 3D collagen matrix. Exploiting the dynamic phase differences method, we for the first time describe dynamics of differences in cell mass distribution in 3D migrating mesenchymal and amoeboid cancer cells, and also demonstrate that certain features are shared by both invasion modes. We found that amoeboid fibrosarcoma cells' membrane blebbing is enhanced upon constriction and is also occasionally present in mesenchymally invading cells around constricted nuclei. Further, we demonstrate that both leading protrusions and leading pseudopods of invading fibrosarcoma cells are defined by higher cell mass density. In addition, we directly document bundling of collagen fibres by protrusions of mesenchymal fibrosarcoma cells. Thus, such a non-invasive microscopy offers a novel insight into cellular events during 3D invasion.

Indexed as

Cell MovementCell Culture TechniquesCell Line, TumorCell MembraneCollagenFibrosarcomaHolographyHumansImaging, Three-DimensionalIntravital MicroscopyNeoplasm InvasivenessPseudopodiaCollagen

Identifiers

PMID30104699
PMCPMC6089916

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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.