Evidence map›Paper›PMID 30500808›Full record

ArticlePLoS genetics2018

Downregulation of ERG and FLI1 expression in endothelial cells triggers endothelial-to-mesenchymal transition.

Nao Nagai, Hiroto Ohguchi, Ryo Nakaki, Yoshihiro Matsumura, Yasuharu Kanki, Juro Sakai, Hiroyuki Aburatani, Takashi Minami

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 8% 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

48 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

  1. Pooled it
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  16. Single cell 'omic profiles of human aortic endothelial cellsbioRxiv : the preprint server for biology · 2024
    Article
  17. Article
  18. Article
  19. Transcription factors regulating vasculogenesis and angiogenesis.Developmental dynamics : an official publication of the American Association of Anatomists · 2024
    Review
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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 2 institutions in 1 country.

Nao NagaiDivision of Molecular and Vascular Biology, IRDA, Kumamoto University, Kumamoto, Japan.
Hiroto OhguchiDivision of Disease Epigenetics, IRDA, Kumamoto University, Kumamoto, Japan.
Ryo NakakiDivision of Genome Sciences, RCAST, The University of Tokyo, Tokyo, Japan.
Yoshihiro MatsumuraDivision of Metabolic Medicine, RCAST, The University of Tokyo, Tokyo, Japan.
Yasuharu KankiIsotope Science Center, The University of Tokyo, Tokyo, Japan.
Juro SakaiDivision of Metabolic Medicine, RCAST, The University of Tokyo, Tokyo, Japan.
Hiroyuki AburataniDivision of Genome Sciences, RCAST, The University of Tokyo, Tokyo, Japan.ORCID 0000-0003-0438-1544
Takashi MinamiDivision of Molecular and Vascular Biology, IRDA, Kumamoto University, Kumamoto, Japan.
The University of Tokyo · JPKumamoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endothelial cell (EC) plasticity in pathological settings has recently been recognized as a driver of disease progression. Endothelial-to-mesenchymal transition (EndMT), in which ECs acquire mesenchymal properties, has been described for a wide range of pathologies, including cancer. However, the mechanism regulating EndMT in the tumor microenvironment and the contribution of EndMT in tumor progression are not fully understood. Here, we found that combined knockdown of two ETS family transcription factors, ERG and FLI1, induces EndMT coupled with dynamic epigenetic changes in ECs. Genome-wide analyses revealed that ERG and FLI1 are critical transcriptional activators for EC-specific genes, among which microRNA-126 partially contributes to blocking the induction of EndMT. Moreover, we demonstrated that ERG and FLI1 expression is downregulated in ECs within tumors by soluble factors enriched in the tumor microenvironment. These data provide new insight into the mechanism of EndMT, functions of ERG and FLI1 in ECs, and EC behavior in pathological conditions.

Indexed as

AnimalsDown-RegulationEndothelial CellsEpigenesis, GeneticEpithelial-Mesenchymal TransitionFemaleGene Knockdown TechniquesGenome-Wide Association StudyHumansHuman Umbilical Vein Endothelial CellsMiceMice, Inbred C57BLMicroRNAsNeoplasmsPrognosisProto-Oncogene Protein c-fli-1ERG protein, humanFLI1 protein, humanMicroRNAsMIRN126 microRNA, humanProto-Oncogene Protein c-fli-1Transcriptional Regulator ERG

Identifiers

PMID30500808
PMCPMC6291168
OpenAlexW2902875247

What OpenQuestion holds

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LicenceCC BY
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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.