von Danwitz Marthe, Klümper Niklas, Bernhardt Marit, Cox Alexander, Krausewitz Philipp, Alajati Abdullah, Kristiansen Glen, Ritter Manuel, Ellinger Jörg, Stein Johannes
Department of Urology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.
Center for Integrated Oncology, University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.
Cancers (Basel). 2023 Mar 21;15(6):1890. doi: 10.3390/cancers15061890.
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.
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.
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.
Comprehensive expression analysis and functional data suggest FBXO45 as a prognostic biomarker in PCA.
含F-box/SPRY结构域蛋白1(FBXO45)通过对特定靶点的泛素化和降解在细胞凋亡调控中发挥关键作用。近期研究表明FBXO45在多种癌症中具有预后潜力。然而,其在前列腺癌中的具体作用仍不清楚。
利用癌症基因组图谱数据库和公开可用的基因表达综合数据库进展期前列腺癌队列对前列腺癌中FBXO45 mRNA表达进行系统分析。随后,通过对一个综合组织芯片队列进行免疫组化分析来评估FBXO45蛋白表达。将表达数据与临床病理参数及无生化复发生存情况相关联。免疫组化分析根据TMPRSS2-ERG重排状态进行分层。为评估FBXO45敲低对细胞肿瘤增殖能力和转移潜能的影响,在细胞培养模型中进行反义寡核苷酸转染。
在TCGA队列中,FBXO45 mRNA表达与不良临床病理参数相关,且在进展至远处转移的整个过程中表达增强。FBXO45与无生化复发生存期缩短相关,这在TMPRSS2-ERG阳性肿瘤中尤为明显。在体外,FBXO45敲低导致PC3、DU145和LNCaP细胞培养物的迁移能力显著降低。
综合表达分析和功能数据表明FBXO45是前列腺癌的一种预后生物标志物。