Evidence map›Paper›PMID 26011631›Full record

ArticlePloS one2015

Zearalenone mycotoxin affects immune mediators, MAPK signalling molecules, nuclear receptors and genome-wide gene expression in pig spleen.

Gina Cecilia Pistol, Cornelia Braicu, Monica Motiu, Mihail Alexandru Gras, Daniela Eliza Marin, Mariana Stancu, Loredana Calin, Florentina Israel-Roming, Ioana Berindan-Neagoe, Ionelia Taranu

Open 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. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
15.5field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 99 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

10 authors at 4 institutions in 2 countries.

Gina Cecilia PistolLaboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, 077015, Balotesti, Ilfov, Romania.
Cornelia BraicuOncologic Institute Prof. Dr. I. Chiricuta, 400015, Cluj-Napoca, Romania; Research Center for Functional Genomics, Biomedicine and Translational Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400565, Cluj-Napoca, Romania.
Monica MotiuLaboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, 077015, Balotesti, Ilfov, Romania.
Mihail Alexandru GrasLaboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, 077015, Balotesti, Ilfov, Romania.
Daniela Eliza MarinLaboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, 077015, Balotesti, Ilfov, Romania.
Mariana StancuLaboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, 077015, Balotesti, Ilfov, Romania.
Loredana CalinLaboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, 077015, Balotesti, Ilfov, Romania.
Florentina Israel-RomingBiotechnology Department, University of Agriculture and Veterinary Medicine, 011464, Bucharest, Romania.
Ioana Berindan-NeagoeOncologic Institute Prof. Dr. I. Chiricuta, 400015, Cluj-Napoca, Romania; Research Center for Functional Genomics, Biomedicine and Translational Medicine, "Iuliu Hatieganu" University of Medicine and Pharmacy, 400565, Cluj-Napoca, Romania; Department of Experimental Therapeutics M.D. Anderson Cancer Center, Houston, TX, United States of America.
Ionelia TaranuLaboratory of Animal Biology, National Institute for Research and Development for Biology and Animal Nutrition, 077015, Balotesti, Ilfov, Romania.
National Research Development Institute for Animal Biology and Nutrition · ROInstitute of Oncology Prof. Dr. Ion Chiricuta · ROTherapeuticsMD (United States) · USUniversity of Agronomic Sciences and Veterinary Medicine of Bucharest · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The toxicity of zearalenone (ZEA) was evaluated in swine spleen, a key organ for the innate and adaptative immune response. Weaned pigs were fed for 18 days with a control or a ZEA contaminated diet. The effect of ZEA was assessed on wide genome expression, pro- (TNF-α, IL-8, IL-6, IL-1β, IFN-γ) and anti-inflammatory (IL-10, IL-4) cytokines, other molecules involved in inflammatory processes (MMPs/TIMPs), as well as signaling molecules, (p38/JNK1/JNK2-MAPKs) and nuclear receptors (PPARγ/NFkB/AP-1/STAT3/c-JUN). Microarray analysis showed that 46% of total number of differentially expressed genes was involved in cellular signaling pathway, 13% in cytokine network and 10% in the inflammatory response. ZEA increased expression and synthesis of pro- inflammatory (TNF-α, IL-8, IL-6, IL-1β) and had no effect on IFN-γ, IL-4 and IL-10 cytokines in spleen. The inflammatory stimulation might be a consequence of JNK pathway activation rather than of p-38MAPK and NF-kB involvement whose gene and protein expression were suppressed by ZEA action. In summary, our findings indicated the role of ZEA as an immune disruptor at spleen level.

Indexed as

AnimalsGene ExpressionImmunologic FactorsInflammationInterferon-gammaInterleukinsMAP Kinase Signaling SystemMitogen-Activated Protein KinasesMycotoxinsNF-kappa BReceptors, Cytoplasmic and NuclearSignal TransductionSpleenSwineZearalenoneImmunologic FactorsInterferon-gammaInterleukinsMitogen-Activated Protein KinasesMycotoxinsNF-kappa BReceptors, Cytoplasmic and NuclearZearalenone

Identifiers

PMID26011631
PMCPMC4444191
OpenAlexW1829463977

What OpenQuestion holds

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LicenceCC BY
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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.