Evidence map›Paper›PMID 27041564›Full record

ArticleOncogene2016

The PLA2R1-JAK2 pathway upregulates ERRα and its mitochondrial program to exert tumor-suppressive action.

A Griveau, G Devailly, L Eberst, N Navaratnam, B Le Calvé, M Ferrand, P Faull, A Augert, R Dante, J M Vanacker and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2016. 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
0.6field-weighted citation impact, top 28% 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, 28 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

12 authors at 3 institutions in 2 countries.

A GriveauInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
G DevaillyInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
L EberstInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
N NavaratnamCellular Stress Group, MRC Clinical Sciences Centre, Faculty of Medicine, Imperial College, Hammersmith Campus, London, UK.
B Le CalvéInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
M FerrandInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
P FaullBiological Mass Spectrometry and Proteomics Laboratory, MRC Clinical Sciences Centre, Imperial College London, London, UK.
A AugertInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
R DanteInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
J M VanackerInstitut de Génomique Fonctionnelle de Lyon, Université de Lyon, Université Lyon I, CNRS UMR5242, Ecole Normale Supérieure de Lyon, Lyon, France.
D VindrieuxInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
D BernardInserm U1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France.ORCID 0000-0002-1557-2074
Université Claude Bernard Lyon 1 · FRHammersmith Hospital · GBImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Little is known about the biological role of the phospholipase A2 receptor (PLA2R1) transmembrane protein. In recent years, PLA2R1 has been shown to have an important role in regulating tumor-suppressive responses via JAK2 activation, but the underlying mechanisms are largely undeciphered. In this study, we observed that PLA2R1 increases the mitochondrial content, judged by increased levels of numerous mitochondrial proteins, of the mitochondrial structural component cardiolipin, of the mitochondrial DNA content, and of the mitochondrial DNA replication and transcription factor TFAM. This effect of PLA2R1 relies on a transcriptional program controlled by the estrogen-related receptor alpha1 (ERRα) mitochondrial master regulator. Expression of ERRα and of its nucleus-encoded mitochondrial targets is upregulated upon PLA2R1 ectopic expression, and this effect is mediated by JAK2. Conversely, downregulation of PLA2R1 decreases the level of ERRα and of its nucleus-encoded mitochondrial targets. Finally, blocking the ERRα-controlled mitochondrial program largely inhibits the PLA2R1-induced tumor-suppressive response. Together, our data document ERRα and its mitochondrial program as downstream effectors of the PLA2R1-JAK2 pathway leading to oncosuppression.

Indexed as

Cell Line, TumorDNA-Binding ProteinsERRalpha Estrogen-Related ReceptorGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansJanus Kinase 2MitochondriaMitochondrial ProteinsNeoplasmsReceptors, EstrogenReceptors, Phospholipase A2Transcriptional ActivationTranscription FactorsDNA-Binding ProteinsERRalpha Estrogen-Related ReceptorJAK2 protein, humanJanus Kinase 2Mitochondrial ProteinsPLA2R1 protein, humanReceptors, EstrogenReceptors, Phospholipase A2TFAM protein, humanTranscription Factors

Identifiers

PMID27041564
OpenAlexW2337177550

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.