Evidence map›Paper›PMID 28076331›Full record

Trial reportOncotarget2017

A short-term intervention with selenium affects expression of genes implicated in the epithelial-to-mesenchymal transition in the prostate.

Dieuwertje E G Kok, Lambertus A L M Kiemeney, Gerald W Verhaegh, Jack A Schalken, Emile N J T van Lin, J P Michiel Sedelaar, J Alfred Witjes, Christina A Hulsbergen-van de Kaa, Pieter van 't Veer, Ellen Kampman and 1 more

Open access · diamondAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Vimentin as a target for the treatment of COVID-19.BMJ open respiratory research · 2020
    Article
  9. Review
  10. Article
  11. Review
  12. 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

11 authors at 4 institutions in 2 countries.

Dieuwertje E G KokDivision of Human Nutrition, Wageningen University, Wageningen, The Netherlands.
Lambertus A L M KiemeneyDepartment for Health Evidence, Radboud University Medical Center, Nijmegen, The Netherlands.
Gerald W VerhaeghDepartment of Urology, Radboud university Medical Center, Nijmegen, The Netherlands.
Jack A SchalkenDepartment of Urology, Radboud university Medical Center, Nijmegen, The Netherlands.
Emile N J T van LinStrahlentherapie Bonn Rhein Sieg, Wesel, Germany.
J P Michiel SedelaarDepartment of Urology, Radboud university Medical Center, Nijmegen, The Netherlands.
J Alfred WitjesDepartment of Urology, Radboud university Medical Center, Nijmegen, The Netherlands.
Christina A Hulsbergen-van de KaaDepartment of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.
Pieter van 't VeerDivision of Human Nutrition, Wageningen University, Wageningen, The Netherlands.
Ellen KampmanDivision of Human Nutrition, Wageningen University, Wageningen, The Netherlands.
Lydia A AfmanDivision of Human Nutrition, Wageningen University, Wageningen, The Netherlands.
Radboud University Nijmegen · NLRadboud University Medical Center · NLWageningen University & Research · NLHochschule Bonn-Rhein-Sieg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In parallel with the inconsistency in observational studies and chemoprevention trials, the mechanisms by which selenium affects prostate cancer risk have not been elucidated. We conducted a randomized, placebo-controlled trial to examine the effects of a short-term intervention with selenium on gene expression in non-malignant prostate tissue. Twenty-three men received 300 µg selenium per day in the form of selenized yeast (n=12) or a placebo (n=11) during 5 weeks. Prostate biopsies collected from the transition zone before and after intervention were analysed for 15 participants (n=8 selenium, n=7 placebo). Pathway analyses revealed that the intervention with selenium was associated with down-regulated expression of genes involved in cellular migration, invasion, remodeling and immune responses. Specifically, expression of well-established epithelial markers, such as E-cadherin and epithelial cell adhesion molecule EPCAM, was up-regulated, while the mesenchymal markers vimentin and fibronectin were down-regulated after intervention with selenium. This implies an inhibitory effect of selenium on the epithelial-to-mesenchymal transition (EMT). Moreover, selenium was associated with down-regulated expression of genes involved in wound healing and inflammation; processes which are both related to EMT. In conclusion, our explorative data showed that selenium affected expression of genes implicated in EMT in the transition zone of the prostate.

Indexed as

Dietary SupplementsAgedEpithelial-Mesenchymal TransitionGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksHumansMaleMiddle AgedNetherlandsOligonucleotide Array Sequence AnalysisProstateSeleniumSignal TransductionTime FactorsTranscriptomeSeleniumEMTgene expressionmicroarrayprostatic neoplasmsselenium

Identifiers

PMID28076331
PMCPMC5354681
OpenAlexW2570466966

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.