Evidence map›Paper›PMID 32042016›Full record

ArticleScientific reports2020

SETD3 acts as a prognostic marker in breast cancer patients and modulates the viability and invasion of breast cancer cells.

Nourhan Hassan, Niklas Rutsch, Balázs Győrffy, Nancy Adriana Espinoza-Sánchez, Martin Götte

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 32 citations in OpenAlex.

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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

5 authors at 3 institutions in 3 countries.

Nourhan Hassan *Department of Gynecology and Obstetrics, Münster University Hospital, Albert-Schweitzer-Campus 1, D11, Münster, 48149, Germany.
Niklas Rutsch *Department of Gynecology and Obstetrics, Münster University Hospital, Albert-Schweitzer-Campus 1, D11, Münster, 48149, Germany.
Balázs GyőrffyDepartment of Bioinformatics and 2nd Department of Pediatrics, Semmelweis University, and TTK Momentum Cancer Biomarker Research Group, Budapest, Hungary.
Nancy Adriana Espinoza-SánchezDepartment of Gynecology and Obstetrics, Münster University Hospital, Albert-Schweitzer-Campus 1, D11, Münster, 48149, Germany.ORCID http://orcid.org/0000-0002-4118-6521
Martin GötteDepartment of Gynecology and Obstetrics, Münster University Hospital, Albert-Schweitzer-Campus 1, D11, Münster, 48149, Germany. mgotte@uni-muenster.de.ORCID http://orcid.org/0000-0003-2360-2496
University Hospital Münster · DEHospital Infantil de México Federico Gómez · MXSemmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In several carcinomas, the SET Domain Containing 3, Actin Histidine Methyltransferase (SETD3) is associated with oncogenesis. However, there is little knowledge about the role of SETD3 in the progression and prognosis of breast cancer. In this study, we first analyzed the prognostic value of SETD3 in breast cancer patients using the database of the public Kaplan-Meier plotter. Moreover, in vitro assays were performed to assess the role of SETD3 in the viability and capacity of invasion of human breast cancer cell lines. We observed that the high expression of SETD3 was associated with better relapse-free survival (RFS) of the whole collective of 3,951 patients, of Estrogen Receptor-positive, and of Luminal A-type breast cancer patients. However, in patients lacking expression of estrogen-, progesterone- and HER2-receptor, and those affected by a p53-mutation, SETD3 was associated with poor RFS. In vitro analysis showed that SETD3 siRNA depletion affects the viability of triple-negative cells as well as the cytoskeletal function and capacity of invasion of highly invasive MDA-MB-231 cells. Interestingly, SETD3 regulates the expression of other genes associated with cancer such as β-actin, FOXM1, FBXW7, Fascin, eNOS, and MMP-2. Our study suggests that SETD3 expression can act as a subtype-specific biomarker for breast cancer progression and prognosis.

Indexed as

Biomarkers, TumorBreastBreast NeoplasmsCell Line, TumorCell SurvivalDisease-Free SurvivalDisease ProgressionDNA MethylationEpigenesis, GeneticErb-b2 Receptor Tyrosine KinasesFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesHistone MethyltransferasesHumansKaplan-Meier EstimateBiomarkers, TumorERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesHistone MethyltransferasesReceptors, EstrogenReceptors, ProgesteroneRNA, Small InterferingSETD3 protein, humanTP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID32042016
PMCPMC7010743
OpenAlexW3005522568

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.