Evidence map›Paper›PMID 24806521›Full record

ArticlePloS one2014

Cell invasion in the spheroid sprouting assay: a spatial organisation analysis adaptable to cell behaviour.

Silvia Blacher, Charlotte Erpicum, Bénédicte Lenoir, Jenny Paupert, Gustavo Moraes, Sandra Ormenese, Eric Bullinger, Agnès Noel

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Article
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  5. AXL promotes lymphangiogenesis by amplifying VEGF-C-mediated AKT pathway.Cellular and molecular life sciences : CMLS · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Modeling lymphangiogenesis: Pairing in vitro and in vivo metrics.Microcirculation (New York, N.Y. : 1994) · 2023
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Dynamics of 3D carcinoma cell invasion into aligned collagen.Integrative biology : quantitative biosciences from nano to macro · 2018
    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

8 authors.

Silvia BlacherLaboratory of tumor and developmental biology, GIGA-Cancer, University of Liège, Liège, Belgium.
Charlotte ErpicumLaboratory of tumor and developmental biology, GIGA-Cancer, University of Liège, Liège, Belgium.
Bénédicte LenoirLaboratory of tumor and developmental biology, GIGA-Cancer, University of Liège, Liège, Belgium; Laboratory of cardiovascular research, CRP santé, Luxembourg, Luxembourg.
Jenny PaupertLaboratory of tumor and developmental biology, GIGA-Cancer, University of Liège, Liège, Belgium.
Gustavo MoraesGIGA-Imaging and Flow Cytometry Platform, University of Liege, Liege, Belgium.
Sandra OrmeneseGIGA-Imaging and Flow Cytometry Platform, University of Liege, Liege, Belgium.
Eric BullingerGIGA Systems Biology and Chemical Biology, University of Liege, Liege, Belgium.
Agnès NoelLaboratory of tumor and developmental biology, GIGA-Cancer, University of Liège, Liège, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endothelial cell spheroid assay provides a suitable in vitro model to study (lymph) angiogenesis and test pro- and anti-(lymph) angiogenic factors or drugs. Usually, the extent of cell invasion, observed through optical microscopy, is measured. The present study proposes the spatial distribution of migrated cells as a new descriptor of the (lymph) angiogenic response. The utility of this novel method rests with its capacity to locally characterise spheroid structure, allowing not only the investigation of single and collective cell invasion but also the evolution of the spheroid core itself. Moreover, the proposed method can be applied to 2D-projected spheroid images obtained by optical microscopy, as well as to 3D images acquired by confocal microscopy. To validate the proposed methodology, endothelial cell invasion was evaluated under different experimental conditions. The results were compared with widely used global parameters. The comparison shows that our method prevents local spheroid modifications from being overlooked and leading to the possible misinterpretation of results.

Indexed as

Angiogenesis InhibitorsCell MovementCell TrackingEndothelial CellsHumansImaging, Three-DimensionalMicroscopy, ConfocalNeovascularization, PathologicSpheroids, CellularTelomeraseVascular Endothelial Growth Factor AAngiogenesis InhibitorsTelomeraseTERT protein, humanVascular Endothelial Growth Factor A

Identifiers

PMID24806521
PMCPMC4013117

What OpenQuestion holds

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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.