Evidence map›Paper›PMID 31612022›Full record

ArticleOncology letters2019

Upregulation of SPDEF is associated with poor prognosis in prostate cancer.

Jan Meiners, Katharina Schulz, Katharina Möller, Doris Höflmayer, Christoph Burdelski, Claudia Hube-Magg, Ronald Simon, Cosima Göbel, Andrea Hinsch, Viktor Reiswich and 18 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 14% 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, 16 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

28 authors at 3 institutions in 1 country.

Jan MeinersDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Katharina SchulzDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Katharina MöllerDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Doris HöflmayerDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Christoph BurdelskiDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Claudia Hube-MaggDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Ronald SimonDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Cosima GöbelDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Andrea HinschDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Viktor ReiswichDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Sören WeidemannDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Jacob R IzbickiGeneral, Visceral and Thoracic Surgery Department and Clinic, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Guido SauterDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Frank JacobsenDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Christina Möller-KoopDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Tim MandelkowDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Niclas C BlessinDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Florian LutzDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Florian ViehwegerDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Maximillian LennartzDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Christoph FrauneDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Hans HeinzerProstate Cancer Center, Martini-Clinic, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Sarah MinnerDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Sarah BonkGeneral, Visceral and Thoracic Surgery Department and Clinic, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Hartwig HulandProstate Cancer Center, Martini-Clinic, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Markus GraefenProstate Cancer Center, Martini-Clinic, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Thorsten SchlommDepartment of Urology, Section for Translational Prostate Cancer Research, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Franziska BüscheckDepartment of Pathology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
University Medical Center Hamburg-Eppendorf · DEUniversität Hamburg · DEMartini-Klinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SAM pointed domain-containing Ets transcription factor (SPDEF), a member of the ETS transcription factor family, has been associated with prostate cancer development; however, its role in tumour development and progression is controversial. In the present study, SPDEF expression was analysed on a tissue microarray with >12,000 prostate cancer samples. SPDEF expression levels were higher in most prostate cancer samples than in normal prostate epithelium, suggesting SPDEF was upregulated in cancer. Nuclear SPDEF expression was identified in 80% of prostate cancer samples, and considered weak in 26.4%, moderate in 40.1% and strong in 13.5% of cases. SPDEF positivity was significantly associated with tumour stage, Gleason grade, lymph node metastasis and PSA recurrence (all P<0.0001). SPDEF overexpression was more common in ERG positive (94%) than in ERG negative cancer (69%; P<0.0001). Elevated SPDEF expression predicted poor prognosis independent from established prognostic parameters, including Gleason grade, pT, pN, serum PSA level and nodal status (P<0.01). In summary, SPDEF overexpression was associated with aggressive behaviour, particularly in ERG negative prostate cancer, and may have potential for clinical application.

Indexed as

deletionETS-related geneprostate cancerSAM pointed domain-containing Ets transcription factortissue microarray

Identifiers

PMID31612022
PMCPMC6781494
OpenAlexW2974355375

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.