Evidence map›Paper›PMID 12069687›Full record

ArticleThe Biochemical journal2002

Inhibition of peroxisome proliferator-activated receptor (PPAR)-mediated keratinocyte differentiation by lipoxygenase inhibitors.

Philippe Thuillier, Alan R Brash, James P Kehrer, Julie B Stimmel, Lisa M Leesnitzer, Peiying Yang, Robert A Newman, Susan M Fischer

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 65 citations in OpenAlex.

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  9. Lipid mediators in acne.Mediators of inflammation · 2010
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  10. The role of herbs and spices in cancer prevention.The Journal of nutritional biochemistry · 2008
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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

8 authors at 3 institutions in 1 country.

Philippe ThuillierDepartment of Carcinogenesis, University of Texas M.D. Anderson Cancer Center, Smithville 78957, USA.
Alan R Brash
James P Kehrer
Julie B Stimmel
Lisa M Leesnitzer
Peiying Yang
Robert A Newman
Susan M Fischer
GlaxoSmithKline (United States) · USResearch Triangle Park Foundation · USThe University of Texas at Austin · US

Funding

Pilot Project ProgramP30ES007784 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1996 to 2011
$16.4M
RESEARCH TRAINING IN CARCINOGENESIS &MUTAGENESIST32CA009480 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RICHIE, ELLEN R · 1985 to 2012
$3.0M
8 LOX AND SKIN CANCER SUSCEPTIBILITYR01CA083794 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI FISCHER, SUSAN M · 2000 to 2004
$1.6M
APOPTOSIS,5 LIPOXYGENASE ACTIVATING PROTEIN AND BCL XR01CA083701 · NCI · UNIVERSITY OF TEXAS AUSTIN · PI KEHRER, JAMES P · 2000 to 2004
$1.3M
Skin Cancer Prevention by Dietary Fatty AcidsR01CA112083 · NCI · OREGON HEALTH & SCIENCE UNIVERSITY · PI THUILLIER, PHILIPPE · 2005 to 2008
$929k
NCI NIH HHS CA09480-16NCI NIH HHS CA83701NCI NIH HHS CA83794NCI NIH HHS R01 CA112083NIEHS NIH HHS ES07784NIGMS NIH HHS GM-53638
6 · The paper itself

Abstract

Lipoxygenase (LOX) metabolites from arachidonic acid and linoleic acid have been implicated in atherosclerosis, inflammation, keratinocyte differentiation and tumour progression. We previously showed that peroxisome proliferator-activated receptors (PPARs) play a role in keratinocyte differentiation and that the PPARalpha ligand 8S-hydroxyeicosatetraenoic acid is important in this process. We hypothesized that blocking LOX activity would block PPAR-mediated keratinocyte differentiation. Three LOX inhibitors, nordihydroguaiaretic acid, quercetin and morin, were studied for their effects on primary keratinocyte differentiation and PPAR activity. All three LOX inhibitors blocked calcium-induced expression of the differentiation marker keratin 1. In addition, activity of a PPAR-responsive element was inhibited in the presence of all three inhibitors, and this effect was mediated primarily through PPARalpha and PPARgamma. LOX inhibitors decreased the activity of a chimaeric PPAR-Gal4-ligand-binding domain reporter system and this effect was reversed by addition of PPAR ligands. Ligand-binding studies revealed that the LOX inhibitors bind directly to PPARs and demonstrate a novel mechanism for these inhibitors in altering PPAR-mediated gene expression.

Indexed as

AnimalsArachidonic AcidBlotting, NorthernBlotting, WesternCell DifferentiationCells, CulturedCell SurvivalDose-Response Relationship, DrugEnzyme InhibitorsGenes, ReporterInhibitory Concentration 50KeratinocytesKeratinsLigandsLinoleic AcidLipoxygenaseArachidonic AcidEnzyme InhibitorsKeratinsLigandsLinoleic AcidLipoxygenaseReceptors, Cytoplasmic and NuclearTranscription Factors

Identifiers

PMID12069687
PMCPMC1222830
OpenAlexW1488758018

What OpenQuestion holds

Textmetadata
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.