Evidence map›Paper›PMID 30417891›Full record

ArticleJournal of visualized experiments : JoVE2018

Morphology-Based Distinction Between Healthy and Pathological Cells Utilizing Fourier Transforms and Self-Organizing Maps.

Fabian L Kriegel, Ralf Köhler, Jannike Bayat-Sarmadi, Simon Bayerl, Anja E Hauser, Raluca Niesner, Andreas Luch, Zoltan Cseresnyes

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Self-Organizing Maps for CellularFrontiers in immunology · 2021
    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.

Fabian L KriegelDepartment of Chemical and Product Safety, German Federal Institute for Risk Assessment (BfR); Deutsches Rheuma-Forschungszentrum (DRFZ) Berlin, a Leibniz Institute.
Ralf KöhlerDeutsches Rheuma-Forschungszentrum (DRFZ) Berlin, a Leibniz Institute.
Jannike Bayat-SarmadiDeutsches Rheuma-Forschungszentrum (DRFZ) Berlin, a Leibniz Institute.
Simon BayerlCharité Universitätsmedizin Berlin.
Anja E HauserDeutsches Rheuma-Forschungszentrum (DRFZ) Berlin, a Leibniz Institute; Charité Universitätsmedizin Berlin.
Raluca NiesnerDeutsches Rheuma-Forschungszentrum (DRFZ) Berlin, a Leibniz Institute.
Andreas LuchDepartment of Chemical and Product Safety, German Federal Institute for Risk Assessment (BfR).
Zoltan CseresnyesApplied Systems Biology, Leibniz Institute for Natural Product Research and Infection Biology Hans Knöll Institute; Zoltan.Cseresnyes@hki-jena.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The appearance and the movements of immune cells are driven by their environment. As a reaction to a pathogen invasion, the immune cells are recruited to the site of inflammation and are activated to prevent a further spreading of the invasion. This is also reflected by changes in the behavior and the morphological appearance of the immune cells. In cancerous tissue, similar morphokinetic changes have been observed in the behavior of microglial cells: intra-tumoral microglia have less complex 3-dimensional shapes, having less-branched cellular processes, and move more rapidly than those in healthy tissue. The examination of such morphokinetic properties requires complex 3D microscopy techniques, which can be extremely challenging when executed longitudinally. Therefore, the recording of a static 3D shape of a cell is much simpler, because this does not require intravital measurements and can be performed on excised tissue as well. However, it is essential to possess analysis tools that allow the fast and precise description of the 3D shapes and allows the diagnostic classification of healthy and pathogenic tissue samples based solely on static, shape-related information. Here, we present a toolkit that analyzes the discrete Fourier components of the outline of a set of 2D projections of the 3D cell surfaces via Self-Organizing Maps. The application of artificial intelligence methods allows our framework to learn about various cell shapes as it is applied to more and more tissue samples, whilst the workflow remains simple.

Indexed as

Cell ShapeFourier AnalysisArtificial IntelligenceHumansMicroglia

Identifiers

PMID30417891
PMCPMC6235618

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.