Evidence map›Paper›PMID 25924802›Full record

ArticleClinical & experimental metastasis2015

Nidogen 1 and Nuclear Protein 1: novel targets of ETV5 transcription factor involved in endometrial cancer invasion.

Núria Pedrola, Laura Devis, Marta Llauradó, Irene Campoy, Elena Martinez-Garcia, Marta Garcia, Laura Muinelo-Romay, Lorena Alonso-Alconada, Miguel Abal, Francesc Alameda and 10 more

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In one paragraph

Article in Clinical & experimental metastasis, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 17% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Biomarkers of tumor invasiveness in proteomics (Review).International journal of oncology · 2020
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  10. Prognostic value ofWorld journal of gastrointestinal oncology · 2024
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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

20 authors at 10 institutions in 2 countries.

Núria PedrolaBiomedical Research Group in Ginaecology, Hospital Universitari Vall d'Hebron, Institut de Recerca (VHIR), Universitat Autònoma de Barcelona, Passeig Vall d'Hebron, 119-129, 08035, Barcelona, Spain.
Laura Devis
Marta Llauradó
Irene Campoy
Elena Martinez-Garcia
Marta Garcia
Laura Muinelo-Romay
Lorena Alonso-Alconada
Miguel Abal
Francesc Alameda
Gemma Mancebo
Ramon Carreras
Josep Castellví
Sílvia Cabrera
Antonio Gil-Moreno
Xavier Matias-Guiu
Juan L Iovanna
Eva Colas
Jaume Reventós
Anna Ruiz
Vall d'Hebron Institut de Recerca · ESHospital Del Mar · ESVall d'Hebron Hospital Universitari · ESUniversitat Autònoma de Barcelona · ESComplejo Hospitalario Universitario de Santiago · ESComplexo Hospitalario Universitario A Coruña · ESHospital Arnau de Vilanova · ESInserm · FRServicio Gallego de Salud · ESUniversitat Internacional de Catalunya · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial cancer is the most frequent malignancy of the female genital tract in western countries. Our group has previously characterized the upregulation of the transcription factor ETV5 in endometrial cancer with a specific and significant increase in those tumor stages associated with myometrial invasion. We have shown that ETV5 overexpression in Hec1A endometrial cancer cells induces epithelial to mesenchymal transition resulting in the acquisition of migratory and invasive capabilities. In the present work, we have identified Nidogen 1 (NID1) and Nuclear Protein 1 (NUPR1) as direct transcriptional targets of ETV5 in endometrial cancer cells. Inhibition of NID1 and NUPR1 in ETV5 overexpressing cells reduced cell migration and invasion in vitro and reduced tumor growth and dissemination in an orthotopic endometrial cancer model. Importantly, we confirmed a significant increase of NUPR1 and NID1 protein expression in the invasion front of the tumor compared to their paired superficial zone, concomitant to ETV5 overexpression. Altogether, we conclude that NID1 and NUPR1 are novel targets of ETV5 and are actively cooperating with ETV5 at the invasion front of the tumor in the acquisition of an invasive phenotype to jointly drive endometrial cancer invasion.

Indexed as

Cell MovementCell ProliferationGene Expression Regulation, NeoplasticAnimalsApoptosisBase SequenceBasic Helix-Loop-Helix ProteinsBlotting, WesternChromatin ImmunoprecipitationDNA-Binding ProteinsEndometrial NeoplasmsFemaleHumansImmunoenzyme TechniquesLuciferasesMembrane GlycoproteinsBasic Helix-Loop-Helix ProteinsDNA-Binding ProteinsETV5 protein, humanLuciferasesMembrane GlycoproteinsNeoplasm ProteinsnidogenNUPR1 protein, humanRNA, MessengerTranscription Factors

Identifiers

PMID25924802
OpenAlexW1975001408

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.