Evidence map›Paper›PMID 21780113›Full record

ArticleJournal of cellular physiology2012

PED/PEA-15 controls fibroblast motility and wound closure by ERK1/2-dependent mechanisms.

Roberta Buonomo, Ferdinando Giacco, Angela Vasaturo, Sergio Caserta, Stefano Guido, Valentina Pagliara, Corrado Garbi, Gelsomina Mansueto, Angela Cassese, Giuseppe Perruolo and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cellular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. A Clue on the Skin: A Systematic Review on Immunohistochemical Analyses of the Ligature Mark.International journal of environmental research and public health · 2022
    Pooled it
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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

14 authors at 3 institutions in 1 country.

Roberta BuonomoDepartment of Cellular and Molecular Biology and Pathology, Federico II University of Naples, Naples, Italy.
Ferdinando Giacco
Angela Vasaturo
Sergio Caserta
Stefano Guido
Valentina Pagliara
Corrado Garbi
Gelsomina Mansueto
Angela Cassese
Giuseppe Perruolo
Francesco Oriente
Claudia Miele
Francesco Beguinot
Pietro Formisano
Institute for Experimental Endocrinology and Oncology · ITUniversity of Naples Federico II · ITCeinge Biotecnologie Avanzate (Italy) · IT

Funding

Telethon GGP09012
6 · The paper itself

Abstract

Cell migration is dependent on the control of signaling events that play significant roles in creating contractile force and in contributing to wound closure. We evaluated wound closure in fibroblasts from mice overexpressing (TgPED) or lacking ped/pea-15 (KO), a gene overexpressed in patients with type 2 diabetes. Cultured skin fibroblasts isolated from TgPED mice showed a significant reduction in the ability to recolonize wounded area during scratch assay, compared to control fibroblasts. This difference was observed both in the absence and in the presence of mytomicin C, an inhibitor of mitosis. In time-lapse experiments, TgPED fibroblasts displayed about twofold lower velocity and diffusion coefficient, as compared to controls. These changes were accompanied by reduced spreading and decreased formation of stress fibers and focal adhesion plaques. At the molecular level, TgPED fibroblasts displayed decreased RhoA activation and increased abundance of phosphorylated extracellular signal-regulated kinase 1/2 (ERK1/2). Inhibition of ERK1/2 activity by PD98059 restored RhoA activation, cytoskeleton organization and cell motility, and almost completely rescued wound closure of TgPED fibroblasts. Interestingly, skin fibroblasts isolated from KO mice displayed an increased wound closure ability. In vivo, healing of dorsal wounds was delayed in TgPED and accelerated in KO mice. Thus, PED/PEA-15 may affect fibroblast motility by a mechanism, at least in part, mediated by ERK1/2.

Indexed as

AnimalsApoptosis Regulatory ProteinsCell AdhesionCell MovementCells, CulturedDiabetes Mellitus, Type 2FibroblastsFlavonoidsHistocompatibility Antigens Class IHumansMAP Kinase Signaling SystemMiceMice, KnockoutMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Phosphoproteins2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-oneApoptosis Regulatory ProteinsFlavonoidsHistocompatibility Antigens Class IMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Pea15 protein, mousePhosphoproteinsQ surface antigensrhoA GTP-Binding Protein

Identifiers

PMID21780113
PMCPMC3306794
OpenAlexW2011317119

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.