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

Author:

von Danwitz Marthe12ORCID,Klümper Niklas123ORCID,Bernhardt Marit24,Cox Alexander12ORCID,Krausewitz Philipp12ORCID,Alajati Abdullah12,Kristiansen Glen24ORCID,Ritter Manuel12,Ellinger Jörg12ORCID,Stein Johannes12ORCID

Affiliation:

1. Department of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany

2. Center for Integrated Oncology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany

3. Institute of Experimental Oncology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany

4. Institute of Pathology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany

Abstract

Background: F-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. Methods: A 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. Results: FBXO45 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. Conclusions: Comprehensive expression analysis and functional data suggest FBXO45 as a prognostic biomarker in PCA.

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference38 articles.

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