Evidence map›Paper›PMID 32525929›Full record

ArticlePloS one2020

Bayesian networks established functional differences between breast cancer subtypes.

Lucía Trilla-Fuertes, Angelo Gámez-Pozo, Jorge M Arevalillo, Rocío López-Vacas, Elena López-Camacho, Guillermo Prado-Vázquez, Andrea Zapater-Moros, Mariana Díaz-Almirón, María Ferrer-Gómez, Hilario Navarro and 5 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Methylation ofMedComm · 2023
    Article
  4. Review
  5. Review
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 4 institutions in 2 countries.

Lucía Trilla-FuertesBiomedica Molecular Medicine SL, Madrid, Spain.
Angelo Gámez-PozoBiomedica Molecular Medicine SL, Madrid, Spain.
Jorge M ArevalilloOperational Research and Numerical Analysis, National Distance Education University (UNED), Madrid, Spain.ORCID 0000-0003-1944-3699
Rocío López-VacasMolecular Oncology & Pathology Lab, Institute of Medical and Molecular Genetics-INGEMM, La Paz University Hospital-IdiPAZ, Madrid, Spain.
Elena López-CamachoBiomedica Molecular Medicine SL, Madrid, Spain.
Guillermo Prado-VázquezBiomedica Molecular Medicine SL, Madrid, Spain.
Andrea Zapater-MorosBiomedica Molecular Medicine SL, Madrid, Spain.
Mariana Díaz-AlmirónBiostatistics Unit, La Paz University Hospital-IdiPAZ, Madrid, Spain.
María Ferrer-GómezMolecular Oncology & Pathology Lab, Institute of Medical and Molecular Genetics-INGEMM, La Paz University Hospital-IdiPAZ, Madrid, Spain.
Hilario NavarroOperational Research and Numerical Analysis, National Distance Education University (UNED), Madrid, Spain.
Paolo NanniFunctional Genomics Centre Zurich, University of Zurich/ETH Zurich, Zurich, Switzerland.
Pilar ZamoraMedical Oncology Service, La Paz University Hospital-IdiPAZ, Madrid, Spain.
Enrique EspinosaMedical Oncology Service, La Paz University Hospital-IdiPAZ, Madrid, Spain.
Paloma MaínDepartment of Statistics and Operations Research, Faculty of Mathematics, Complutense University of Madrid, Madrid, Spain.ORCID 0000-0002-7418-5381
Juan Ángel Fresno VaraBiomedica Molecular Medicine SL, Madrid, Spain.ORCID 0000-0003-1527-1252
Hospital Universitario La Paz · ESUniversidad Nacional de Educación a Distancia · ESUniversidad Complutense de Madrid · ESUniversity of Zurich · CH

Funding

A Health IT based Psychoeducational Intervention for African American Prostate CancerR01MD007783 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI RIVERS, BRIAN M. · 2014 to 2019
$1.8M
NIMHD NIH HHS R01 MD007783
6 · The paper itself

Abstract

Breast cancer is a heterogeneous disease. In clinical practice, tumors are classified as hormonal receptor positive, Her2 positive and triple negative tumors. In previous works, our group defined a new hormonal receptor positive subgroup, the TN-like subtype, which had a prognosis and a molecular profile more similar to triple negative tumors. In this study, proteomics and Bayesian networks were used to characterize protein relationships in 96 breast tumor samples. Components obtained by these methods had a clear functional structure. The analysis of these components suggested differences in processes such as mitochondrial function or extracellular matrix between breast cancer subtypes, including our new defined subtype TN-like. In addition, one of the components, mainly related with extracellular matrix processes, had prognostic value in this cohort. Functional approaches allow to build hypotheses about regulatory mechanisms and to establish new relationships among proteins in the breast cancer context.

Indexed as

ProteomicsBayes TheoremBreast NeoplasmsExtracellular MatrixGene OntologyHumansPrognosis

Identifiers

PMID32525929
PMCPMC7289386
OpenAlexW3034229506

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.