Evidence map›Paper›PMID 18444964›Full record

ArticlePigment cell & melanoma research2008

PPAR gamma regulates MITF and beta-catenin expression and promotes a differentiated phenotype in mouse melanoma S91.

Maja Grabacka, Wojciech Placha, Krystyna Urbanska, Piotr Laidler, Przemysław M Płonka, Krzysztof Reiss

Open access · greenAbstract read
In one paragraph

Article in Pigment cell & melanoma research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 42 citations in OpenAlex.

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  7. Fenofibrate subcellular distribution as a rationale for the intracranial delivery through biodegradable carrier.Journal of physiology and pharmacology : an official journal of the Polish Physiological Society · 2015
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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

6 authors at 3 institutions in 2 countries.

Maja GrabackaDepartment of Food Biotechnology, Faculty of Food Technology, Agricultural University of Krakow, Krakow, Poland. mgrabacka@ar.krakow.pl
Wojciech Placha
Krystyna Urbanska
Piotr Laidler
Przemysław M Płonka
Krzysztof Reiss
Jagiellonian University · PLTemple University · USUniversity of Agriculture in Krakow · PL

Funding

Nuclear IRS-1-DNA repair and mutagenesis in medulloblastomaR01CA095518 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI REISS, KRZYSZTOF · 2002 to 2012
$2.6M
NCI NIH HHS R01 CA095518
6 · The paper itself

Abstract

Melanoma represents one of the most rapidly metastasizing, hence deadly tumors due to its high proliferation rate and invasiveness, characteristics of undifferentiated embryonic tissues. Given the absence of effective therapy for metastatic melanoma, understanding more fully the molecular mechanisms underlying melanocyte differentiation may provide opportunities for novel therapeutic intervention. Here we show that in mouse melanoma S91 cells activation of the peroxisome proliferator activated receptor (PPAR) gamma induces events resembling differentiation, such as growth arrest accompanied by apoptosis, spindle morphology and enhanced tyrosinase expression. These events are preceded by an initial transient increase in expression from the Microphthalmia-associated transcription factor gene, (MITF) promoter, whereas exposure to a PPAR gamma ligand- ciglitazone that exceeds 8 h, causes a gradual decrease of MITF, until by 48 h MITF expression is substantially reduced. Beta-catenin, an MITF transcriptional activator, shows a similar pattern of decline during ciglitazone treatment, consistent with previous reports that activated PPAR gamma inhibits the Wnt/beta-catenin pathway through induction of beta-catenin proteasomal degradation. We suggest that the PPAR gamma-mediated beta-catenin down-regulation is likely to be responsible for changes in MITF levels. The data suggest that PPAR gamma, besides its well-established role in mesenchymal cell differentiation towards adipocytes, might regulate differentiation in the melanocytic lineage.

Indexed as

Cell DifferentiationGene Expression Regulation, NeoplasticAlitretinoinAnimalsAntigens, DifferentiationAntineoplastic Agentsbeta CateninBlotting, WesternCell CycleCell Line, TumorCell ShapeFluorescent Antibody TechniqueMelanocytesMelanomaMiceMicrophthalmia-Associated Transcription FactorAlitretinoinAntigens, DifferentiationAntineoplastic Agentsbeta CateninciglitazoneMicrophthalmia-Associated Transcription FactorMonophenol MonooxygenasePPAR gammaThiazolidinedionesTretinoin

Identifiers

PMID18444964
PMCPMC3951148
OpenAlexW2005957228

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.