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PITX1 Is a Regulator of TERT Expression in Prostate Cancer with Prognostic Power

Authors :
Koenig, Alexandra M. Poos
Cornelia Schroeder
Neeraja Jaishankar
Daniela Röll
Marcus Oswald
Jan Meiners
Delia M. Braun
Caroline Knotz
Lukas Frank
Manuel Gunkel
Roman Spilger
Thomas Wollmann
Adam Polonski
Georgia Makrypidi-Fraune
Christoph Fraune
Markus Graefen
Inn Chung
Alexander Stenzel
Holger Erfle
Karl Rohr
Aria Baniahmad
Guido Sauter
Karsten Rippe
Ronald Simon
Rainer
Source :
Cancers; Volume 14; Issue 5; Pages: 1267
Publication Year :
2022
Publisher :
Multidisciplinary Digital Publishing Institute, 2022.

Abstract

The current risk stratification in prostate cancer (PCa) is frequently insufficient to adequately predict disease development and outcome. One hallmark of cancer is telomere maintenance. For telomere maintenance, PCa cells exclusively employ telomerase, making it essential for this cancer entity. However, TERT, the catalytic protein component of the reverse transcriptase telomerase, itself does not suit as a prognostic marker for prostate cancer as it is rather low expressed. We investigated if, instead of TERT, transcription factors regulating TERT may suit as prognostic markers. To identify transcription factors regulating TERT, we developed and applied a new gene regulatory modeling strategy to a comprehensive transcriptome dataset of 445 primary PCa. Six transcription factors were predicted as TERT regulators, and most prominently, the developmental morphogenic factor PITX1. PITX1 expression positively correlated with telomere staining intensity in PCa tumor samples. Functional assays and chromatin immune-precipitation showed that PITX1 activates TERT expression in PCa cells. Clinically, we observed that PITX1 is an excellent prognostic marker, as concluded from an analysis of more than 15,000 PCa samples. PITX1 expression in tumor samples associated with (i) increased Ki67 expression indicating increased tumor growth, (ii) a worse prognosis, and (iii) correlated with telomere length.

Details

Language :
English
ISSN :
20726694
Database :
OpenAIRE
Journal :
Cancers; Volume 14; Issue 5; Pages: 1267
Accession number :
edsair.multidiscipl..4e17f0a607da48ffcf306b0bd3d0b846
Full Text :
https://doi.org/10.3390/cancers14051267