TRIM24 as an independent prognostic biomarker for prostate cancer.


Journal

Urologic oncology
ISSN: 1873-2496
Titre abrégé: Urol Oncol
Pays: United States
ID NLM: 9805460

Informations de publication

Date de publication:
09 2019
Historique:
received: 13 02 2019
revised: 08 05 2019
accepted: 13 05 2019
pubmed: 11 6 2019
medline: 12 9 2020
entrez: 11 6 2019
Statut: ppublish

Résumé

Simply applicable biomarkers for prostate cancer patients predicting the clinical course are urgently needed. Recently, TRIM24 has been identified to promote androgen receptor signaling and to correlate with an aggressive prostate cancer phenotype. Based on these data, we proofed TRIM24 as a prognostic biomarker for risk stratification. We performed TRIM24 immunohistochemistry on 2 independent cohorts including a total of 806 primary tumors, 26 locally advanced/recurrent tumors, 30 lymph node metastases, 30 distant metastases, and 129 benign prostatic samples from 497 patients as well as on 246 prostate needle biopsies. Expression data were correlated with clinic-pathological data including biochemical recurrence-free survival (bRFS) as endpoint. Benign samples show no or low TRIM24 expression in 94%, while tumor tissues demonstrate significant higher levels. Strongest expression is observed in advanced and metastatic tumors. In multivariate analyses, TRIM24 up-regulation on radical prostatectomy specimens correlates with shorter bRFS independent of other prognostic parameters. 5-(10-) year bRFS rates for TRIM24 negative, low, medium and high expressing tumors are 93.1(93.1)%, 75.4(68.5)%, 54.9(47.5)% and 43.1(32.3)%, respectively. Of interest, tumors diagnosed as indolent disease, TRIM24 expression stratifies patients into specific risk groups. Increased TRIM24 expression associates with higher grade group, positive nodal status and extraprostatic tumor growth. TRIM24 assessment on prostate needle biopsies taken prior to treatment decision at time of initial diagnosis significantly correlates with recurrence after surgery. Using 2 large independent radical prostatectomy specimen cohorts, we found that TRIM24 expression predicts patients' risk to develop disease recurrence with high accuracy and independent from other established biomarkers. Further, this is the first study exploring TRIM24 expression on prostate needle biopsies which represents the clinically relevant tissue type on which biomarkers guide treatment decisions. Thus, we strongly suggest introducing TRIM24 evaluation in prostate needle biopsies in clinical routine as an inexpensive and simple immunohistochemical test.

Identifiants

pubmed: 31178279
pii: S1078-1439(19)30192-9
doi: 10.1016/j.urolonc.2019.05.006
pii:
doi:

Substances chimiques

Biomarkers, Tumor 0
Carrier Proteins 0
TRIM24 protein, human 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

576.e1-576.e10

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Anne Offermann (A)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Doris Roth (D)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Marie Christine Hupe (MC)

Department of Urology, University Hospital Schleswig-Holstein, Germany.

Silke Hohensteiner (S)

Department of Pathology, Klinik am Eichert Alb Fils Kliniken, Goeppingen, Germany.

Finn Becker (F)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Vincent Joerg (V)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Jessica Carlsson (J)

Department of Urology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Christiane Kuempers (C)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Julika Ribbat-Idel (J)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Lars Tharun (L)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Verena Sailer (V)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Jutta Kirfel (J)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Maria Svensson (M)

Department of Research and Education, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Ove Andren (O)

Department of Urology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.

Verena Lubczyk (V)

Department of Pathology, Klinik am Eichert Alb Fils Kliniken, Goeppingen, Germany.

Rainer Kuefer (R)

Department of Urology, Klinik am Eichert Alb Fils Kliniken, Goeppingen, Germany.

Axel S Merseburger (AS)

Department of Urology, University Hospital Schleswig-Holstein, Germany.

Sven Perner (S)

Institute of Pathology, University Hospital Schleswig-Holstein, Luebeck, Germany; Pathology of the Research Center Borstel, Leibniz Lung Center, Borstel, Germany. Electronic address: sven.perner@uksh.de.

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Classifications MeSH