Evidence map›Paper›PMID 30241392›Full record

ArticleInternational journal of molecular sciences2018

The Role of PPARβ/δ in Melanoma Metastasis.

Jonathan Chee Woei Lim, Yuet Ping Kwan, Michelle Siying Tan, Melissa Hui Yen Teo, Shunsuke Chiba, Walter Wahli, Xiaomeng Wang

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

20 citing papers in PubMed, 27 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

7 authors at 3 institutions in 4 countries.

Jonathan Chee Woei LimLee Kong Chian School of Medicine, Nanyang Technological University Singapore, 59 Nanyang Drive, Singapore 636921, Singapore. cheewoei@upm.edu.my.
Yuet Ping KwanLee Kong Chian School of Medicine, Nanyang Technological University Singapore, 59 Nanyang Drive, Singapore 636921, Singapore. kwanyuetping@ntu.edu.sg.
Michelle Siying TanLee Kong Chian School of Medicine, Nanyang Technological University Singapore, 59 Nanyang Drive, Singapore 636921, Singapore. michelle.siying@ntu.edu.sg.
Melissa Hui Yen TeoLee Kong Chian School of Medicine, Nanyang Technological University Singapore, 59 Nanyang Drive, Singapore 636921, Singapore. teohy@imcb.a-star.edu.sg.
Shunsuke ChibaDivision of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore 637371, Singapore. Shunsuke@ntu.edu.sg.ORCID 0000-0003-2039-023X
Walter WahliLee Kong Chian School of Medicine, Nanyang Technological University Singapore, 59 Nanyang Drive, Singapore 636921, Singapore. walter.wahli@ntu.edu.sg.ORCID 0000-0002-5966-9089
Xiaomeng WangLee Kong Chian School of Medicine, Nanyang Technological University Singapore, 59 Nanyang Drive, Singapore 636921, Singapore. wangxiaomeng@ntu.edu.sg.
Nanyang Technological University · SGAgency for Science, Technology and Research · SGUniversiti Putra Malaysia · MY

Funding

Lee Kong Chian School of Medicine, Nanyang Technological University Singapore Start-upMinistry of Education - Singapore MOE2014-T2-1-036
6 · The paper itself

Abstract

backgroundPeroxisome proliferator⁻activated receptor (PPAR) β/δ, a ligand-activated transcription factor, is involved in diverse biological processes including cell proliferation, cell differentiation, inflammation and energy homeostasis. Besides its well-established roles in metabolic disorders, PPARβ/δ has been linked to carcinogenesis and was reported to inhibit melanoma cell proliferation, anchorage-dependent clonogenicity and ectopic xenograft tumorigenicity. However, PPARβ/δ's role in tumour progression and metastasis remains controversial.

methodsIn the present studies, the consequence of PPARβ/δ inhibition either by global genetic deletion or by a specific PPARβ/δ antagonist, 10h, on malignant transformation of melanoma cells and melanoma metastasis was examined using both in vitro and in vivo models.

resultsOur study showed that 10h promotes epithelial-mesenchymal transition (EMT), migration, adhesion, invasion and trans-endothelial migration of mouse melanoma B16/F10 cells. We further demonstrated an increased tumour cell extravasation in the lungs of wild-type mice subjected to 10h treatment and in

conclusionThese results indicated a protective role of PPARβ/δ in melanoma progression and metastasis.

Indexed as

AnimalsCell Line, TumorEpithelial-Mesenchymal TransitionMelanomaMiceNeoplasm InvasivenessNeoplasm MetastasisPPAR-betaPPAR deltaPPAR-betaPPAR deltaEMTinvasionmelanomametastasismigrationperoxisome proliferator–activated receptor β/δ

Identifiers

PMID30241392
PMCPMC6213649
OpenAlexW2891838265

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.