Evidence map›Paper›PMID 19917608›Full record

ArticleThe Journal of biological chemistry2010

Role of HuR and p38MAPK in ultraviolet B-induced post-transcriptional regulation of COX-2 expression in the human keratinocyte cell line HaCaT.

Niklas S Fernau, Dominik Fugmann, Martin Leyendecker, Kerstin Reimann, Susanne Grether-Beck, Stefanie Galban, Niloofar Ale-Agha, Jean Krutmann, Lars-Oliver Klotz

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.2field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 58 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

9 authors at 1 institution in 1 country.

Niklas S FernauFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Dominik FugmannFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Martin LeyendeckerFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Kerstin ReimannFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Susanne Grether-BeckFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Stefanie GalbanFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Niloofar Ale-AghaFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Jean KrutmannFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany.
Lars-Oliver KlotzFrom the Leibniz-Institut für Umweltmedizinische Forschung, D-40225 Düsseldorf, Germany. Electronic address: LarsOliver.Klotz@uni-duesseldorf.de.
Leibniz Institute for Neurobiology · DE

Funding

Control of Apoptosis and Signaling by XIAPR01GM067827 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DUCKETT, COLIN S. · 2005 to 2009
$1.3M
NIGMS NIH HHS R01 GM067827
6 · The paper itself

Abstract

COX-2 (cyclooxygenase-2) is a pivotal player in inflammatory processes, and ultraviolet radiation is a known stimulus for COX-2 expression in skin cells. Here, an induction of COX-2 expression in HaCaT human keratinocytes was observed only upon exposure of cells to UVB (280-320 nm) but not to UVA radiation (320-400 nm), as demonstrated by reverse transcription-PCR and Western blotting. Prostaglandin E(2) levels were elevated in cell culture supernatants of HaCaT cells exposed to UVB. COX-2 mRNA stability was dramatically increased by UVB irradiation. Both the stabilization of COX-2 mRNA and the enhancement of COX-2 steady-state mRNA and protein levels caused by UVB were prevented both by inhibition and small interfering RNA-induced depletion of p38(MAPK), a kinase strongly activated upon exposure to UVB, suggesting p38(MAPK)-dependent mRNA stabilization as a mechanism of UVB-induced COX-2 expression. A dramatic decrease in COX-2 expression induced by UVB was elicited by small interfering RNA-based depletion of a stress-responsive mRNA stabilizing protein regulated by p38(MAPK), i.e. HuR; UVB-induced elevation of COX-2 mRNA and protein levels coincided with an accumulation of HuR in the cytoplasm and was attenuated in cells depleted of HuR. Moreover, UVB-induced generation of prostaglandin E(2) by HaCaT cells was blunted by HuR depletion, suggesting that stress kinases (such as p38(MAPK)) as well as HuR are excellent targets for approaches aiming at interfering with induction of COX-2 expression by UVB.

Indexed as

Ultraviolet RaysAntigens, SurfaceBlotting, WesternCell LineCell SurvivalCyclooxygenase 2CytoplasmDinoprostoneDose-Response Relationship, RadiationELAV-Like Protein 1ELAV ProteinsGene Expression RegulationGene Expression Regulation, EnzymologicHumansIndolesKeratinocytesAntigens, SurfacebisindolylmaleimideCyclooxygenase 2DinoprostoneELAVL1 protein, humanELAV-Like Protein 1ELAV ProteinsIndolesMaleimidesp38 Mitogen-Activated Protein KinasesProtein Kinase CPTGS2 protein, humanRNA-Binding Proteins

Identifiers

PMID19917608
PMCPMC2823532
OpenAlexW2052323063

What OpenQuestion holds

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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.