| Literature DB >> 32314536 |
Christoph Fraune1, Serhiy Yehorov1, Andreas M Luebke1, Stefan Steurer1, Claudia Hube-Magg1, Franziska Büscheck1, Doris Höflmayer1, Maria Christina Tsourlakis1, Till S Clauditz1, Ronald Simon1, Guido Sauter1, Sören Weidemann1, David Dum1, Simon Kind1, Sarah Minner1, Thorsten Schlomm2, Hartwig Huland3, Hans Heinzer3, Markus Graefen3, Eike Burandt1.
Abstract
Pituitary tumor-transforming gene 1 (PTTG1) is a regulator of chromosome stability. PTTG1 overexpression had been associated with tumor aggressiveness in several cancer types. To examine its prognostic utility in prostate cancer, a tissue microarray including 12 427 tumors with clinical and molecular data was analyzed by immunohistochemistry. PTTG1 immunostaining was largely absent in normal prostate epithelial cells. In cancers, staining was considered weak in 5.4%, moderate in 5.6% and strong in 0.8%. Strong staining was linked to advanced pT stage, high classical and quantitative Gleason grade, high Ki67-labeling index (all P < 0.0001) and lymph node metastasis (P = 0.0083). The prognostic impact of PTTG1 expression was independent of established preoperative and postoperative prognostic features. Comparison with molecular features revealed that PTTG1 upregulation was associated with nine of 12 common genomic deletions (P < 0.05), p53 alterations and high androgen receptor levels (P < 0.001 each), but was unrelated to the TMPRSS2:ERG fusion status. In conclusion, these data identify PTTG1 as a strong and independent prognostic feature in prostate cancer. PTTG1 measurement, either alone or in combination with other biomarkers might be instrumental for determining prostate cancer aggressiveness.Entities:
Keywords: ERG; PTTG1; TMA; prostate cancer
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Year: 2020 PMID: 32314536 DOI: 10.1111/pin.12938
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534