Evidence map›Paper›PMID 29309407›Full record

ArticlePLoS computational biology2018

Bowhead: Bayesian modelling of cell velocity during concerted cell migration.

Mathias Engel, James Longden, Jesper Ferkinghoff-Borg, Xavier Robin, Gaye Saginc, Rune Linding

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 22% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 1 country.

Mathias EngelBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-0728-2605
James LongdenBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Jesper Ferkinghoff-BorgBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Xavier RobinBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-6813-3200
Gaye SagincBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.
Rune LindingBiotech Research and Innovation Centre, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-0420-4839
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell migration is a central biological process that requires fine coordination of molecular events in time and space. A deregulation of the migratory phenotype is also associated with pathological conditions including cancer where cell motility has a causal role in tumor spreading and metastasis formation. Thus cell migration is of critical and strategic importance across the complex disease spectrum as well as for the basic understanding of cell phenotype. Experimental studies of the migration of cells in monolayers are often conducted with 'wound healing' assays. Analysis of these assays has traditionally relied on how the wound area changes over time. However this method does not take into account the shape of the wound. Given the many options for creating a wound healing assay and the fact that wound shape invariably changes as cells migrate this is a significant flaw. Here we present a novel software package for analyzing concerted cell velocity in wound healing assays. Our method encompasses a wound detection algorithm based on cell confluency thresholding and employs a Bayesian approach in order to estimate concerted cell velocity with an associated likelihood. We have applied this method to study the effect of siRNA knockdown on the migration of a breast cancer cell line and demonstrate that cell velocity can track wound healing independently of wound shape and provides a more robust quantification with significantly higher signal to noise ratios than conventional analyses of wound area. The software presented here will enable other researchers in any field of cell biology to quantitatively analyze and track live cell migratory processes and is therefore expected to have a significant impact on the study of cell migration, including cancer relevant processes. Installation instructions, documentation and source code can be found at http://bowhead.lindinglab.science licensed under GPLv3.

Indexed as

Cell MovementGene Expression Regulation, NeoplasticAlgorithmsBayes TheoremBreast NeoplasmsCell Cycle ProteinsCell Line, TumorComputational BiologyFemaleHumansMolecular Motor ProteinsMyosin Heavy ChainsNormal DistributionOctamer Transcription Factor-3PhenotypePolo-Like Kinase 1Cell Cycle ProteinsMolecular Motor ProteinsMYH9 protein, humanMyosin Heavy ChainsOctamer Transcription Factor-3Polo-Like Kinase 1POU5F1 protein, humanProtein Serine-Threonine KinasesProto-Oncogene ProteinsRNA, Small Interfering

Identifiers

PMID29309407
PMCPMC5774831
OpenAlexW2782613412

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.