Evidence map›Paper›PMID 25352548›Full record

ArticleNucleic acids research2014

Resveratrol post-transcriptionally regulates pro-inflammatory gene expression via regulation of KSRP RNA binding activity.

Franziska Bollmann, Julia Art, Jenny Henke, Katharina Schrick, Verena Besche, Matthias Bros, Huige Li, Daniel Siuda, Norbert Handler, Florian Bauer and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

36 citing papers in PubMed, 63 citations in OpenAlex.

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  14. Drug Candidates for Autoimmune Diseases.Pharmaceuticals (Basel, Switzerland) · 2022
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  20. E3 Ligase FBXW2 Is a New Therapeutic Target in Obesity and Atherosclerosis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    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

21 authors at 7 institutions in 3 countries.

Franziska BollmannDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Julia ArtDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Jenny HenkeDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Katharina SchrickDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Verena BescheDepartment of Dermatology, Johannes Gutenberg-University Medical Center, Mainz, Germany Core Facility Lentiviral Transduction Service, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Matthias BrosDepartment of Dermatology, Johannes Gutenberg-University Medical Center, Mainz, Germany Core Facility Lentiviral Transduction Service, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Huige LiDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Daniel SiudaDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Norbert HandlerDepartment of Pharmaceutical/Medicinal Chemistry, University of Vienna, Vienna, Austria.
Florian BauerDepartment of Pharmaceutical/Medicinal Chemistry, University of Vienna, Vienna, Austria.
Thomas ErkerDepartment of Pharmaceutical/Medicinal Chemistry, University of Vienna, Vienna, Austria.
Felix BehnkeChair of Pharmaceutical/Medicinal Chemistry, Institute of Pharmacy, Friedrich-Schiller-University, Jena, Germany.
Bettina Mönchpharmazentrum frankfurt/ZAFES, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.
Lorena HärdleInstitute of Immunology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Markus HoffmannDepartment of Biochemistry & Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.
Ching-Yi ChenDepartment of Pharmacognosy, University of Vienna, Vienna, Austria.
Ulrich FörstermannDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany.
Verena M DirschPharmaceutical Institute, University Tuebingen, Tuebingen, Germany.
Oliver Werzpharmazentrum frankfurt/ZAFES, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.
Hartmut KleinertDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany kleinert@uni-mainz.de.
Andrea PautzDepartment of Pharmacology, Johannes Gutenberg-University Medical Center, Mainz, Germany pautz@uni-mainz.de.
University Medical Center of the Johannes Gutenberg University Mainz · DEUniversity of Vienna · ATGoethe University Frankfurt · DEJohannes Gutenberg University Mainz · DEFriedrich Schiller University Jena · DEUniversity of Alabama at Birmingham · USUniversity of Tübingen · DE

Funding

Austrian Science Fund FWF P 18982Howard Hughes Medical Institute
6 · The paper itself

Abstract

Resveratrol shows beneficial effects in inflammation-based diseases like cancer, cardiovascular and chronic inflammatory diseases. Therefore, the molecular mechanisms of the anti-inflammatory resveratrol effects deserve more attention. In human epithelial DLD-1 and monocytic Mono Mac 6 cells resveratrol decreased the expression of iNOS, IL-8 and TNF-α by reducing mRNA stability without inhibition of the promoter activity. Shown by pharmacological and siRNA-mediated inhibition, the observed effects are SIRT1-independent. Target-fishing and drug responsive target stability experiments showed selective binding of resveratrol to the RNA-binding protein KSRP, a central post-transcriptional regulator of pro-inflammatory gene expression. Knockdown of KSRP expression prevented resveratrol-induced mRNA destabilization in human and murine cells. Resveratrol did not change KSRP expression, but immunoprecipitation experiments indicated that resveratrol reduces the p38 MAPK-related inhibitory KSRP threonine phosphorylation, without blocking p38 MAPK activation or activity. Mutation of the p38 MAPK target site in KSRP blocked the resveratrol effect on pro-inflammatory gene expression. In addition, resveratrol incubation enhanced KSRP-exosome interaction, which is important for mRNA degradation. Finally, resveratrol incubation enhanced its intra-cellular binding to the IL-8, iNOS and TNF-α mRNA. Therefore, modulation of KSRP mRNA binding activity and, thereby, enhancement of mRNA degradation seems to be the common denominator of many anti-inflammatory effects of resveratrol.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalCell Line, TumorExosome Multienzyme Ribonuclease ComplexGene ExpressionHumansInflammation MediatorsMiceMice, KnockoutMutationp38 Mitogen-Activated Protein KinasesResveratrolRNA-Binding ProteinsRNA, MessengerRNA StabilityStilbenesAnti-Inflammatory Agents, Non-SteroidalExosome Multienzyme Ribonuclease ComplexInflammation MediatorsKHSRP protein, humanKhsrp protein, mousep38 Mitogen-Activated Protein KinasesResveratrolRNA-Binding ProteinsRNA, MessengerStilbenesTrans-Activators

Identifiers

PMID25352548
PMCPMC4227754
OpenAlexW2167188821

What OpenQuestion holds

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Registered trials

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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.