Evidence map›Paper›PMID 24638100›Full record

ArticlePloS one2014

Snail family members unequally trigger EMT and thereby differ in their ability to promote the neoplastic transformation of mammary epithelial cells.

Baptiste Gras, Laurent Jacqueroud, Anne Wierinckx, Christelle Lamblot, Frédérique Fauvet, Joël Lachuer, Alain Puisieux, Stéphane Ansieau

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

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  15. Correlations of mRNA Levels among Efflux Transporters, Transcriptional Regulators, and Scaffold Proteins in Non-Small-Cell Lung Cancer.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2021
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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.

Baptiste GrasInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France.
Laurent JacqueroudInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France.
Anne WierinckxInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France; ProfileXpert, Bron, France.
Christelle LamblotInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France.
Frédérique FauvetInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France.
Joël LachuerInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France; ProfileXpert, Bron, France.
Alain PuisieuxInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France; Institut Universitaire de France, Paris, France.
Stéphane AnsieauInserm UMR-S1052, Centre de Recherche en Cancérologie de Lyon, Lyon, France; CNRS UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France; LabEx DEVweCAN, Lyon, France; UNIV UMR1052, Lyon, France; Université de Lyon, Lyon, France; Centre Léon Bérard, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

By fostering cell commitment to the epithelial-to-mesenchymal transition (EMT), SNAIL proteins endow cells with motility, thereby favoring the metastatic spread of tumor cells. Whether the phenotypic change additionally facilitates tumor initiation has never been addressed. Here we demonstrate that when a SNAIL protein is ectopically produced in non-transformed mammary epithelial cells, the cells are protected from anoikis and proliferate under low-adherence conditions: a hallmark of cancer cells. The three SNAIL proteins show unequal oncogenic potential, strictly correlating with their ability to promote EMT. SNAIL3 especially behaves as a poor EMT-inducer comforting the concept that the transcription factor functionally diverges from its two related proteins.

Indexed as

Epithelial-Mesenchymal TransitionBreast NeoplasmsCell AdhesionCell SurvivalCell Transformation, NeoplasticEpithelial CellsFemaleGene Expression Regulation, NeoplasticHumansMammary Glands, HumanRNA, MessengerSnail Family Transcription FactorsTelomeraseTranscription FactorsRNA, MessengerSnail Family Transcription FactorsTelomeraseTranscription Factors

Identifiers

PMID24638100
PMCPMC3956896

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.