Evidence map›Paper›PMID 26114549›Full record

ArticlePloS one2015

Transcriptome-based identification of new anti-inflammatory and vasodilating properties of the n-3 fatty acid docosahexaenoic acid in vascular endothelial cell under proinflammatory conditions [corrected].

Marika Massaro, Rosanna Martinelli, Valentina Gatta, Egeria Scoditti, Mariangela Pellegrino, Maria Annunziata Carluccio, Nadia Calabriso, Tonia Buonomo, Liborio Stuppia, Carlo Storelli and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Marika MassaroNational Research Council (CNR), Institute of Clinical Physiology, Lecce, Italy.
Rosanna MartinelliCEINGE Biotecnologie Avanzate, Naples, Italy; Department of Medicine and Surgery of Salerno University, Salerno, Italy.
Valentina Gatta"Gabriele d'Annunzio" University and Center of Excellence on Aging, Chieti, Italy.
Egeria ScodittiNational Research Council (CNR), Institute of Clinical Physiology, Lecce, Italy.
Mariangela PellegrinoNational Research Council (CNR), Institute of Clinical Physiology, Lecce, Italy; Department of Biological and Environmental Science and Technology (Disteba), University of Salento, Lecce, Italy.
Maria Annunziata CarluccioNational Research Council (CNR), Institute of Clinical Physiology, Lecce, Italy.
Nadia CalabrisoNational Research Council (CNR), Institute of Clinical Physiology, Lecce, Italy.
Tonia BuonomoCEINGE Biotecnologie Avanzate, Naples, Italy.
Liborio Stuppia"Gabriele d'Annunzio" University and Center of Excellence on Aging, Chieti, Italy.
Carlo StorelliDepartment of Biological and Environmental Science and Technology (Disteba), University of Salento, Lecce, Italy.
Raffaele De Caterina"Gabriele d'Annunzio" University and Center of Excellence on Aging, Chieti, Italy; Fondazione Toscana "Gabriele Monasterio", Pisa, Italy.
Istituto di Fisiologia Clinica · ITUniversity of Chieti-Pescara · ITCeinge Biotecnologie Avanzate (Italy) · ITNational Research Council · ITUniversity of Salento · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

scopeHigh intakes of n-3 fatty acids exert anti-inflammatory effects and cardiovascular protection, but the underlying molecular basis is incompletely defined. By genome-wide analysis we searched for novel effects of docosahexaenoic acid (DHA) on gene expression and pathways in human vascular endothelium under pro-inflammatory conditions. METHODS AND

resultsHuman umbilical vein endothelial cells were treated with DHA and then stimulated with interleukin(IL)-1β. Total RNA was extracted, and gene expression examined by DNA microarray. DHA alone altered the expression of 188 genes, decreasing 92 and increasing 96. IL-1β changed the expression of 2031 genes, decreasing 997 and increasing 1034. Treatment with DHA before stimulation significantly affected the expression of 116 IL-1β-deregulated genes, counter-regulating the expression of 55 genes among those decreased and of 61 among those increased. Functional and network analyses identified immunological, inflammatory and metabolic pathways as the most affected. Newly identified DHA-regulated genes are involved in stemness, cellular growth, cardiovascular system function and cancer, and included cytochrome p450 4F2(CYP4F2), transforming growth factor(TGF)-β2, Cluster of Differentiation (CD)47, caspase recruitment domain(CARD)11 and phosphodiesterase(PDE)5α.

conclusionsEndothelial exposure to DHA regulates novel genes and related pathways. Such unbiased identification should increase our understanding of mechanisms by which n-3 fatty acids affect human diseases.

Indexed as

TranscriptomeCARD Signaling Adaptor ProteinsCD47 AntigenDocosahexaenoic AcidsEndothelial CellsGene Expression ProfilingGene Expression RegulationGene Knockdown TechniquesGene Regulatory NetworksGuanylate CyclaseHumansHuman Umbilical Vein Endothelial CellsInflammation MediatorsInterleukin-1betaSignal TransductionVasodilator AgentsCARD11 protein, humanCARD Signaling Adaptor ProteinsCD47 AntigenDocosahexaenoic AcidsGuanylate CyclaseInflammation MediatorsInterleukin-1betaVasodilator Agents

Identifiers

PMID26114549
PMCPMC4482638
OpenAlexW2197683093

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.