Evidence map›Paper›PMID 36980776›Full record

ArticleCancers2023

Identification of F-Box/SPRY Domain-Containing Protein 1 (FBXO45) as a Prognostic Biomarker for TMPRSS2-ERG-Positive Primary Prostate Cancers.

Marthe von Danwitz, Niklas Klümper, Marit Bernhardt, Alexander Cox, Philipp Krausewitz, Abdullah Alajati, Glen Kristiansen, Manuel Ritter, Jörg Ellinger, Johannes Stein

Open access · goldFull text read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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

10 authors at 1 institution in 1 country.

Marthe von DanwitzDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.ORCID 0000-0003-0366-8068
Niklas KlümperDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.ORCID 0000-0002-3258-0586
Marit BernhardtCenter for Integrated Oncology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.
Alexander CoxDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.ORCID 0000-0001-7837-5740
Philipp KrausewitzDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.ORCID 0000-0002-8213-9975
Abdullah AlajatiDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.
Glen KristiansenCenter for Integrated Oncology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.ORCID 0000-0003-4149-5487
Manuel RitterDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.
Jörg EllingerDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.ORCID 0000-0002-7526-0857
Johannes SteinDepartment of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.ORCID 0000-0002-6316-1229
University of Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundF-box/SPRY domain-containing protein 1 (FBXO45) plays a crucial role in the regulation of apoptosis via the ubiquitylation and degradation of specific targets. Recent studies indicate the prognostic potential of FBXO45 in several cancers. However, its specific role in prostate carcinoma remains unclear.

methodsA systematic analysis of FBXO45 mRNA expression in PCA was performed using The Cancer Genome Atlas database and a publicly available Gene Expression Omnibus progression PCA cohort. Subsequently, FBXO45 protein expression was assessed via immunohistochemical analysis of a comprehensive tissue microarray cohort. The expression data were correlated with the clinicopathological parameters and biochemical-free survival. The immunohistochemical analyses were stratified according to the TMPRSS2-ERG rearrangement status. To assess the impact of FBXO45 knockdown on the tumour proliferation capacity of cells and metastatic potential, transfection with antisense-oligonucleotides was conducted within a cell culture model.

resultsFBXO45 mRNA expression was associated with adverse clinicopathological parameters in the TCGA cohort and was enhanced throughout progression to distant metastasis. FBXO45 was associated with shortened biochemical-free survival, which was pronounced for the TMPRSS2-ERG-positive tumours. In vitro, FBXO45 knockdown led to a significant reduction in migration capacity in the PC3, DU145 and LNCaP cell cultures.

conclusionsComprehensive expression analysis and functional data suggest FBXO45 as a prognostic biomarker in PCA.

Indexed as

apoptosisFBXO45prognostic biomarkerprostate cancer

Identifiers

PMID36980776
PMCPMC10046786
OpenAlexW4353072678

What Socratic holds

Textfull text, public
LicenceCC BY
measurements read23
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 Socratic graph.