Evidence map›Paper›PMID 26284587›Full record

ArticleOncotarget2015

Differential involvement of RASSF2 hypermethylation in breast cancer subtypes and their prognosis.

Noemi Perez-Janices, Idoia Blanco-Luquin, Natalia Torrea, Therese Liechtenstein, David Escors, Alicia Cordoba, Francisco Vicente-Garcia, Isabel Jauregui, Susana De La Cruz, José Juan Illarramendi and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

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

  1. Pooled it
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  14. DNA methylation in endometriosis (Review).Molecular medicine reports · 2016
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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

16 authors at 6 institutions in 2 countries.

Noemi Perez-JanicesCancer Epigenetics Group, Navarrabiomed-Fundación Miguel Servet (FMS), Instituto de Investigaciones Sanitarias de Navarra-IdiSNA, Navarra, Spain.
Idoia Blanco-LuquinCancer Epigenetics Group, Navarrabiomed-Fundación Miguel Servet (FMS), Instituto de Investigaciones Sanitarias de Navarra-IdiSNA, Navarra, Spain.
Natalia TorreaWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
Therese LiechtensteinDivision of Infection and Immunity, Rayne Institute, University College London (UCL), London, United Kingdom.
David EscorsDivision of Infection and Immunity, Rayne Institute, University College London (UCL), London, United Kingdom.
Alicia CordobaDepartment of Pathology, Complejo Hospitalario de Navarra, Navarra Health Service, Pamplona, Navarra, Spain.
Francisco Vicente-GarciaDepartment of Surgery, Complejo Hospitalario de Navarra, Navarra Health Service, Navarra, Spain.
Isabel JaureguiDepartment of Pathology, Complejo Hospitalario de Navarra, Navarra Health Service, Pamplona, Navarra, Spain.
Susana De La CruzDepartment of Medical Oncology, Complejo Hospitalario de Navarra, Navarra Health Service, Navarra, Spain.
José Juan IllarramendiDepartment of Medical Oncology, Complejo Hospitalario de Navarra, Navarra Health Service, Navarra, Spain.
Valle CocaBiobank Unit, Navarrabiomed-Fundacion Miguel Servet, IdiSNA, Navarra, Spain.
Maria BerdascoCancer Epigenetics Group, Cancer Epigenetics and Biology Programme (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), Barcelona, Spain.
Grazyna KochanWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
Berta IbañezRed de Evaluación en Servicios Sanitarios y Enfermedades Cronicas (REDISSEC), Navarrabiomed-Fundación Miguel Servet, IdiSNA, Navarra, Spain.
José Miguel LeraDepartment of Surgery, Complejo Hospitalario de Navarra, Navarra Health Service, Navarra, Spain.
David Guerrero-SetasCancer Epigenetics Group, Navarrabiomed-Fundación Miguel Servet (FMS), Instituto de Investigaciones Sanitarias de Navarra-IdiSNA, Navarra, Spain.
Complejo Hospitalario de Navarra · ESNavarrabiomed · ESUniversity College London · GBUniversity of Edinburgh · GBInstitut d'Investigació Biomédica de Bellvitge · ESWellcome Centre for Cell Biology · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is a heterogeneous disease that can be subdivided into clinical, histopathological and molecular subtypes (luminal A-like, luminal B-like/HER2-negative, luminal B-like/HER2-positive, HER2-positive, and triple-negative). The study of new molecular factors is essential to obtain further insights into the mechanisms involved in the tumorigenesis of each tumor subtype. RASSF2 is a gene that is hypermethylated in breast cancer and whose clinical value has not been previously studied. The hypermethylation of RASSF1 and RASSF2 genes was analyzed in 198 breast tumors of different subtypes. The effect of the demethylating agent 5-aza-2'-deoxycytidine in the re-expression of these genes was examined in triple-negative (BT-549), HER2 (SK-BR-3), and luminal cells (T-47D). Different patterns of RASSF2 expression for distinct tumor subtypes were detected by immunohistochemistry. RASSF2 hypermethylation was much more frequent in luminal subtypes than in non-luminal tumors (p = 0.001). The re-expression of this gene by lentiviral transduction contributed to the differential cell proliferation and response to antineoplastic drugs observed in luminal compared with triple-negative cell lines. RASSF2 hypermethylation is associated with better prognosis in multivariate statistical analysis (P = 0.039). In conclusion, RASSF2 gene is differently methylated in luminal and non-luminal tumors and is a promising suppressor gene with clinical involvement in breast cancer.

Indexed as

DNA MethylationGene Expression Regulation, NeoplasticAdultAgedAged, 80 and overAntineoplastic AgentsAzacitidineBreast NeoplasmsCell Line, TumorCell ProliferationFemaleGene Expression ProfilingHEK293 CellsHumansHydroxamic AcidsImmunohistochemistryAntineoplastic AgentsAzacitidineHydroxamic AcidsRASSF1 protein, humanRASSF2 protein, humantrichostatin ATumor Suppressor Proteinsbreast cancerDNA methylationprognosisRASSF1RASSF2

Identifiers

PMID26284587
PMCPMC4695163
OpenAlexW1857779813

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.