Evidence map›Paper›PMID 28233816›Full record

ArticleScientific reports2017

High expression of PDGFR-β in prostate cancer stroma is independently associated with clinical and biochemical prostate cancer recurrence.

Yngve Nordby, Elin Richardsen, Mehrdad Rakaee, Nora Ness, Tom Donnem, Hiten R H Patel, Lill-Tove Busund, Roy M Bremnes, Sigve Andersen

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 2 pooled it
6.1field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 2 syntheses or guidelines pooled it, 75 citations in OpenAlex.

  1. PDGFR-βAging · 2021
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  15. Tumor biomarkers for diagnosis, prognosis and targeted therapy.Signal transduction and targeted therapy · 2024
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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

9 authors at 2 institutions in 1 country.

Yngve NordbyDept Clinical Medicine, The Arctic University of Norway, Tromso, Norway.
Elin RichardsenDept Clinical Pathology, University Hospital of North Norway, Tromso, Norway.
Mehrdad RakaeeDept Medical Biology, The Arctic University of Norway, Tromso, Norway.
Nora NessDept Medical Biology, The Arctic University of Norway, Tromso, Norway.
Tom DonnemDept Clinical Medicine, The Arctic University of Norway, Tromso, Norway.
Hiten R H PatelDept Clinical Medicine, The Arctic University of Norway, Tromso, Norway.
Lill-Tove BusundDept Clinical Pathology, University Hospital of North Norway, Tromso, Norway.
Roy M BremnesDept Clinical Medicine, The Arctic University of Norway, Tromso, Norway.
Sigve AndersenDept Clinical Medicine, The Arctic University of Norway, Tromso, Norway.
UiT The Arctic University of Norway · NOUniversity Hospital of North Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to a lack of sufficient diagnostic tools to predict aggressive disease, there is a significant overtreatment of patients with prostate cancer. Platelet derived growth factors (PDGFs) and their receptors (PDGFRs) are key regulators of mesenchymal cells in the tumor microenvironment, and has been associated with unfavorable outcome in several other cancers. Herein, we aimed to investigate the prognostic impact of PDGFR-β and its ligands (PDGF-B and PDGF-D) in a multicenter prostatectomy cohort of 535 Norwegian patients. Using tissue microarrays and immunohistochemistry, the expression of ligands PDGF-B and PDGF-D and their corresponding receptor, PDGFR-β, was assessed in neoplastic tissue and tumor-associated stroma. PDGFR-β was expressed in benign and tumor associated stroma, but not in epithelium. High stromal expression of PDGFR-β was independently associated with clinical relapse (HR = 2.17, p = 0.010) and biochemical failure (HR = 1.58, p = 0.002). This large study highlights the prognostic importance of PDGFR-β expression, implicating its involvement in prostate cancer progression even in early stage disease. Hence, analyses of PDGFR-β may help distinguish which patients will benefit from radical treatment, and since PDGFR-β is associated with relapse and shorter survival, it mandates a focus as a therapeutic target.

Indexed as

Gene Expression Regulation, NeoplasticAgedAged, 80 and overBiomarkers, TumorEpithelial CellsHumansImmunohistochemistryLymphokinesMaleMiddle AgedNeoplasm Recurrence, LocalOrgan SpecificityPlatelet-Derived Growth FactorPrognosisProstateProstatectomyBiomarkers, TumorLymphokinesPDGFD protein, humanPlatelet-Derived Growth FactorProto-Oncogene Proteins c-sisReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID28233816
PMCPMC5324133
OpenAlexW2590280648

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.