Naslov
Pan-cancer analysis of the Mediator complex transcriptome identifies CDK19 and CDK8 as therapeutic targets in advanced prostate cancer

Autori
Brägelmann, Johannes ; Klümper, Niklas ; Offermann, Anne ; von Mässenhausen, Anne ; Böhm, Diana ; Deng, Mario ; Queisser, Angela ; Sanders, Christine ; Syring, Isabella ; S Merseburger, Axel ; Vogel, Wenzel ; Sievers, Elisabeth ; Vlašić, Ignacija ; Carlsson, Jessica ; Andrén, Ove ; Brossart, Peter ; Duensing, Stefan ; A Svensson, Maria ; Shaikhibrahim, Zaki ; Kirfel, Jutta ; Perner, Sven

Izvornik
Clinical cancer research (1078-0432) 23 (2017), 7; 1829-1840

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Mediator complex ; prostate cancer ; TCGA ; CDK8 ; CDK19

Sažetak
PURPOSE: The Mediator complex is a multi-protein assembly, which serves as a hub for diverse signaling pathways to regulate gene expression. Since gene expression is frequently altered in cancer a systematic understanding of the Mediator complex in malignancies could foster the development of novel targeted therapeutic approaches. EXPERIMENTAL DESIGN: We performed a systematic deconvolution of the Mediator subunit expression profiles across 23 cancer entities (n=8568) using data from The Cancer Genome Atlas (TCGA). Prostate cancer (PCa) specific findings were validated in two publicly available gene expression cohorts and a large cohort of primary and advanced PCa (n=622) stained by immunohistochemistry. The role of CDK19 and CDK8 was evaluated by siRNA mediated gene knock-down and inhibitor treatment in PCa cell lines with functional assays and gene expression analysis by RNAseq. RESULTS: Cluster analysis of TCGA expression data segregated tumor entities, indicating tumor-type specific Mediator complex compositions. Only PCa was marked by high expression of CDK19. In primary PCa CDK19 was associated with increased aggressiveness and shorter disease free survival. During cancer progression highest levels of CDK19 and of its paralog CDK8 were present in metastases. In vitro, inhibition of CDK19 and CDK8 by knock-down or treatment with a selective CDK8/CDK19 inhibitor significantly decreased migration and invasion. CONCLUSIONS: Our analysis revealed distinct transcriptional expression profiles of the Mediator complex across cancer entities indicating differential modes of transcriptional regulation. Moreover it identified CDK19 and CDK8 to be specifically overexpressed during PCa progression, highlighting their potential as novel therapeutic targets in advanced PCa.

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Temeljne medicinske znanosti

POVEZANOST RADA