Evidence map›Paper›PMID 32352613›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2020

Fascin regulates protrusions and delamination to mediate invasive, collective cell migration in vivo.

Maureen C Lamb, Kelsey K Anliker, Tina L Tootle

Open access · greenAbstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Maureen C LambAnatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.ORCID 0000-0002-4522-1910
Kelsey K AnlikerAnatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.
Tina L TootleAnatomy and Cell Biology, University of Iowa Carver College of Medicine, Iowa City, Iowa, USA.ORCID 0000-0002-1515-9538
University of Iowa · US

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Prostaglandins control development by coordinating actin cytoskeletal remodelingR01GM116885 · NIGMS · UNIVERSITY OF IOWA · PI TOOTLE, TINA L · 2016 to 2020
$1.6M
NIGMS NIH HHS R01 GM116885NIH HHS P40 OD018537University of Iowa
6 · The paper itself

Abstract

backgroundThe actin bundling protein Fascin is essential for developmental cell migrations and promotes cancer metastasis. In addition to bundling actin, Fascin has several actin-independent roles; how these other functions contribute to cell migration remains unclear. Border cell migration during Drosophila oogenesis provides an excellent model to study Fascin's various roles during invasive, collective cell migration.

resultsOn-time border cell migration during Stage 9 requires Fascin (Drosophila Singed). Fascin functions not only within the migrating border cells, but also within the nurse cells, the substrate for this migration. Fascin genetically interacts with the actin elongation factor Enabled to promote on-time Stage 9 migration and overexpression of Enabled suppresses the defects seen with loss of Fascin. Loss of Fascin results in increased, shorter and mislocalized protrusions during migration. Additionally, loss of Fascin inhibits border cell delamination and increases E-Cadherin (Drosophila Shotgun) adhesions on both the border cells and nurse cells.

conclusionsOverall, Fascin promotes on-time border cell migration during Stage 9 and contributes to multiple aspects of this invasive, collective cell migration, including both protrusion dynamics and delamination. These findings have implications beyond Drosophila, as border cell migration has emerged as a model to study mechanisms mediating cancer metastasis.

Indexed as

Cell MovementActinsAnimalsAnimals, Genetically ModifiedCadherinsCarrier ProteinsCell AdhesionDrosophila melanogasterDrosophila ProteinsFemaleGreen Fluorescent ProteinsMaleMicrofilament ProteinsMicroscopy, ConfocalOocytesOogenesisActinsCadherinsCarrier ProteinsDrosophila ProteinsfascinGreen Fluorescent ProteinsMicrofilament Proteinsborder cellDrosophilaE-CadherinEnabledFascinmigration

Identifiers

PMID32352613
PMCPMC8900984
OpenAlexW3021963171

What OpenQuestion holds

Textmetadata
LicenceTDM
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.