Evidence map›Paper›PMID 26933805›Full record

ArticleOncotarget2016

MicroRNA deregulation in triple negative breast cancer reveals a role of miR-498 in regulating BRCA1 expression.

Nerea Matamala, Maria Teresa Vargas, Ricardo González-Cámpora, Jose Ignacio Arias, Primitiva Menéndez, Eduardo Andrés-León, Kira Yanowsky, Ana Llaneza-Folgueras, Rebeca Miñambres, Beatriz Martínez-Delgado and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 9% 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

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

  1. Pooled it
  2. Review
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  7. Review
  8. Unveiling the vulnerabilities of synthetic lethality in triple-negative breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  9. Article
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  14. Review
  15. Article
  16. Review
  17. Cancers · 2020
    Article
  18. Role and mechanism of miR-187 in human cancer.American journal of translational research · 2020
    Review
  19. Review
  20. Article
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 8 institutions in 1 country.

Nerea MatamalaHuman Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Maria Teresa VargasPathology Service, Hospital Virgen de la Macarena, Sevilla, Spain.
Ricardo González-CámporaPathology Service, Hospital Virgen de la Macarena, Sevilla, Spain.
Jose Ignacio AriasSurgery Service, Hospital Monte Naranco, Oviedo, Spain.
Primitiva MenéndezPathology Service, Hospital Monte Naranco, Oviedo, Spain.
Eduardo Andrés-LeónBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Kira YanowskyHuman Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Ana Llaneza-FolguerasGeneral Surgery Service, Hospital Universitario Central de Asturias, Oviedo, España.
Rebeca MiñambresProjects Unit, Sistemas Genómicos, Valencia, Spain.
Beatriz Martínez-DelgadoMolecular Genetics Unit, Research Institute of Rare Diseases (IIER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Javier BenítezHuman Cancer Genetics Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Hospital Monte Naranco · ESHospital Universitario Virgen Macarena · ESInstituto de Salud Carlos III · ESCentre for Biomedical Network Research on Rare Diseases · ESHospital Universitario Central de Asturias · ESInstituto de Parasitología y Biomedicina "López - Neyra" · ESSistemas Genómicos · ESSpanish National Cancer Research Centre · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence suggests that BRCA1 pathway contributes to the behavior of sporadic triple negative breast cancer (TNBC), but little is known about the mechanisms underlying this association. Considering the central role that microRNAs (miRNAs) play in gene expression regulation, the aim of this study was to identify miRNAs specifically deregulated in TNBC and investigate their involvement in BRCA1 regulation. Using locked nucleic acid (LNA)-based microarrays, expression levels of 1919 miRNAs were measured in paraffin-embedded tissues from 122 breast tumors and 11 healthy breast tissue samples. Differential miRNA expression was explored among the main subtypes of breast cancer, and 105 miRNAs were identified as specific for triple negative tumors. In silico prediction revealed that miR-498 and miR-187-5p target BRCA1, and these results were confirmed by luciferase reporter assay. While miR-187-5p was found overexpressed in a luminal B cell line, miR-498 was highly expressed in a triple negative cell line, Hs578T, and its expression was negatively correlated with the levels of BRCA1. We functionally demonstrated that miR-498 inhibits BRCA1 in breast cancer cell lines, and showed that inhibition of miR-498 led to reduced proliferation in the triple negative cell line Hs578T. Our results indicate that miR-498 regulates BRCA1 expression in breast cancer and its overexpression could contribute to the pathogenesis of sporadic TNBC via BRCA1 downregulation.

Indexed as

Gene Expression Regulation, NeoplasticApoptosisBiomarkers, TumorBRCA1 ProteinCase-Control StudiesCell ProliferationCells, CulturedFemaleHumansMicroRNAsTriple Negative Breast NeoplasmsBiomarkers, TumorBRCA1 ProteinBRCA1 protein, humanMicroRNAsMIRN498 microRNA, humanBRCA1microRNAtriple negative breast cancer

Identifiers

PMID26933805
PMCPMC4991439
OpenAlexW2289532611

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.