Evidence map›Paper›PMID 34765560›Full record

ArticleFrontiers in oncology2021

Involvement of the TGF-β Signaling Pathway in the Development of YAP-Driven Osteosarcoma Lung Metastasis.

Sarah Morice, Geoffroy Danieau, Robel Tesfaye, Mathilde Mullard, Régis Brion, Maryne Dupuy, Benjamin Ory, Bénédicte Brounais-Le Royer, Isabelle Corre, Françoise Redini and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-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

10 citing papers in PubMed, 16 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

11 authors at 3 institutions in 1 country.

Sarah MoriceUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Geoffroy DanieauUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Robel TesfayeUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Mathilde MullardUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Régis BrionUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Maryne DupuyUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Benjamin OryUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Bénédicte Brounais-Le RoyerUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Isabelle CorreUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Françoise RediniUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Franck VerrecchiaUniversité de Nantes, Institut National de la Santé et de la Recherche Médicale Unité Mixte de Recherche (INSERM UMR) 1238, Nantes, France.
Nantes Université · FRInserm · FRCentre Hospitalier Universitaire de Nantes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe poor survival rate of patients with osteosarcoma (OS), specifically with metastases at diagnosis, undergoes the urgency to develop new therapeutic strategies. Although we recently demonstrated the key role of YAP/TEAD signaling in the growth of OS primary tumor, the molecular mechanisms by which YAP regulates metastases development remain poorly understood.

methodsThe molecular mechanisms by which YAP regulates metastases development were studied using an overexpression of mutated forms of YAP able or not able to interact with TEAD. Molecular signatures were identified using RNA-sequencing analysis and gene set enrichment. Interactions between YAP and Smad3 were studied using proximity ligation assay (PLA), immunoprecipitation, and promoter/specific gene assays. The involvement of the TGF-β pathway in the ability of YAP to stimulate metastatic development

resultsOur work shows that a high YAP expression is associated with the presence of lung metastases which predicts a poor prognosis. Molecular analysis indicates that TGF-β signaling is involved in YAP-driven osteosarcoma cell pro-migratory phenotype, epithelial mesenchymal transition, cell migration, and

conclusionsWe demonstrated the crucial involvement of the TGF-β/Smad3 signaling pathway in YAP-driven lung metastasis development in OS.

Indexed as

Hippolung metastasesosteosarcomaTEADTGF-β/Smad3YAP

Identifiers

PMID34765560
PMCPMC8576330
OpenAlexW3208051718

What OpenQuestion holds

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Registered trials

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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.