Evidence map›Paper›PMID 26729869›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Autoregulatory loop of nuclear corepressor 1 expression controls invasion, tumor growth, and metastasis.

Olaia A Martínez-Iglesias, Elvira Alonso-Merino, Sara Gómez-Rey, Juan Pedro Velasco-Martín, Rosa Martín Orozco, Enrique Luengo, Rosa García Martín, Inmaculada Ibáñez de Cáceres, Agustín F Fernández, Mario F Fraga and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
8.4field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
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  7. Transcriptional Repression of Aerobic Glycolysis by OVOL2 in Breast Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2022
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  12. Thyroid Hormone Receptor β Inhibits Self-Renewal Capacity of Breast Cancer Stem Cells.Thyroid : official journal of the American Thyroid Association · 2020
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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

15 authors at 7 institutions in 1 country.

Olaia A Martínez-IglesiasInstituto de Investigaciones Biomédicas "Alberto Sols," Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
Elvira Alonso-MerinoInstituto de Investigaciones Biomédicas "Alberto Sols," Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
Sara Gómez-ReyInstituto de Investigaciones Biomédicas "Alberto Sols," Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
Juan Pedro Velasco-MartínDepartamento de Anatomía, Histología y Neurociencia, Facultad de Medicina, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
Rosa Martín OrozcoInstituto de Investigaciones Biomédicas "Alberto Sols," Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
Enrique LuengoInstituto de Investigaciones Biomédicas "Alberto Sols," Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
Rosa García MartínDepartamento de Anatomía Patológica, Hospital Universitario 12 de Octubre, 28041 Madrid, Spain;
Inmaculada Ibáñez de CáceresEpigenetics Laboratory, Instituto de Genética Médica y Molecular, Biomarkers and Experimental Therapeutics in Cancer, Instituto de Investigación, Hospital Universitario La Paz, 28046 Madrid, Spain;
Agustín F FernándezInstituto Universitario de Oncología del Principado de Asturias, Universidad de Oviedo, 33006 Principado de Asturias, Spain;
Mario F FragaNanomaterials and Nanotechnology Research Center (Centro de Investigación en Nanomateriales y Nanotecnología-Consejo Superior de Investigaciones Científicas), Universidad de Oviedo, 33940 Principado de Asturias, Spain;
Pilar González-PeramatoDepartamento de Anatomía Patológica, Hospital Universitario La Paz, 28046 Madrid, Spain;
Constantino VaronaDepartamento de Anatomía Patológica, Hospital Universitario Ramón y Cajal, Instituto de Investigación Sanitaria Ramón y Cajal (Instituto Ramón y Cajal de Investigación Sanitaria), Universidad de Alcalá, 28034 Madrid, Spain.
José PalaciosDepartamento de Anatomía Patológica, Hospital Universitario Ramón y Cajal, Instituto de Investigación Sanitaria Ramón y Cajal (Instituto Ramón y Cajal de Investigación Sanitaria), Universidad de Alcalá, 28034 Madrid, Spain.
Javier RegaderaDepartamento de Anatomía, Histología y Neurociencia, Facultad de Medicina, Universidad Autónoma de Madrid, 28029 Madrid, Spain;
Ana ArandaInstituto de Investigaciones Biomédicas "Alberto Sols," Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28029 Madrid, Spain; aaranda@iib.uam.es.
Universidad Autónoma de Madrid · ESInstituto de Investigaciones Biomédicas Sols-Morreale · ESHospital Universitario La Paz · ESInstituto Ramón y Cajal de Investigación Sanitaria · ESHospital Universitario 12 De Octubre · ESNanomaterials and Nanotechnology Research Center · ESUniversidad de Oviedo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nuclear corepressor 1 (NCoR) associates with nuclear receptors and other transcription factors leading to transcriptional repression. We show here that NCoR depletion enhances cancer cell invasion and increases tumor growth and metastatic potential in nude mice. These changes are related to repressed transcription of genes associated with increased metastasis and poor prognosis in patients. Strikingly, transient NCoR silencing leads to heterochromatinization and stable silencing of the NCoR gene, suggesting that NCoR loss can be propagated, contributing to tumor progression even in the absence of NCoR gene mutations. Down-regulation of the thyroid hormone receptor β1 (TRβ) appears to be associated with cancer onset and progression. We found that expression of TRβ increases NCoR levels and that this induction is essential in mediating inhibition of tumor growth and metastasis by this receptor. Moreover, NCoR is down-regulated in human hepatocarcinomas and in the more aggressive breast cancer tumors, and its expression correlates positively with that of TRβ. These data provide a molecular basis for the anticancer actions of this corepressor and identify NCoR as a potential molecular target for development of novel cancer therapies.

Indexed as

HomeostasisAgedAnimalsBreast NeoplasmsCell Line, TumorCell ProliferationDNA MethylationEpigenesis, GeneticFemaleGene Expression Regulation, NeoplasticGene SilencingHeterochromatinHumansLiver NeoplasmsMaleMice, NudeHeterochromatinNCOR1 protein, humanNCOR2 protein, humanNuclear Receptor Co-Repressor 1Nuclear Receptor Co-Repressor 2RNA, Small InterferingThyroid Hormone Receptors betametastasisnuclear corepressor 1thyroid hormone receptortranscriptiontumor growth

Identifiers

PMID26729869
PMCPMC4725484
OpenAlexW2230458223

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.