Up-regulation of POM121 is linked to prostate cancer aggressiveness and serves as a prognostic biomarker

被引:3
|
作者
Becker, Finn [1 ]
Offermann, Anne [1 ,2 ]
Roesch, Marie C. [3 ]
Joerg, Vincent [1 ]
Roth, Doris [1 ]
Lubczyk, Verena [4 ]
Kuefer, Rainer [5 ]
Sailer, Verena [1 ]
Kirfel, Jutta [1 ]
Merseburger, Axel S. [3 ]
Perner, Sven [1 ,2 ]
机构
[1] Univ Hosp Schleswig Holstein, Pathol, Campus Luebeck, Lubeck, Germany
[2] Leibniz Lung Ctr, Res Ctr Borstel, Borstel, Germany
[3] Univ Hosp Schleswig Holstein, Dept Urol, Lubeck, Germany
[4] Alb Fils Kliniken, Dept Pathol, Klin Eichert, Goeppingen, Germany
[5] Alb Fils Kliniken, Klin Eichert, Dept Urol, Goeppingen, Germany
关键词
Prostate cancer; Biomarker; Nuclear pore complex; Nucleoporins; POM121; Androgen receptor; NUCLEAR-PORE COMPLEX; GENE; MECHANISMS;
D O I
10.1016/j.urolonc.2022.05.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Nucleoporins as components of the nuclear pore complex (NCP) are known for regulating nuclear-cytoplasmatic transport. Recently, the nucleoporin POM121 was found to have an important impact on intranuclear translocation of prostate cancer (PCa)-specific tumor drivers including the androgen receptor (AR). The aim of our study was to assess the potential of POM121 as a prognostic biomarker. Methods: Therefore, we performed immunohistochemistry (IHC) for POM121 on a large clinically, well characterized PCa tissue cohort comprising benign prostatic samples, radical prostatectomy (RPE) samples, lymph node metastases, local recurrent tumors and distant metastases of 289 patients. Using a semi automated tissue image analysis software we evaluated POM121 protein expression level based on IHC. Results: We could show that POM121 expression increases during tumor progression. Expression levels were significantly higher in pri-mary tumors compared to benign samples (P = 0.001), and substantially higher in advanced tumors (P < 0.001) and in distant metastases (P = 0.006) compared to primary tumors. Furthermore, POM121 expression predicts biochemical recurrence free survival (BFS) after sur-gery independent of the WHO group and other clinicopathological markers. 5-years BFS with primary tumors lacking POM121 and expressing POM121 was 88.8% and 68.9%, respectively. Conclusion: Our study reveals the potential of POM121 as a potential biomarker for PCa, predicting BFS independent of other common clinicopathological parameters. Furthermore, POM121 might be a new targetable structure for patients suffering from advanced PCa. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:380.e11 / 380.e18
页数:8
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