Scientific Reports (May 2017)

Up regulation and nuclear translocation of Y-box binding protein 1 (YB-1) is linked to poor prognosis in ERG-negative prostate cancer

  • Asmus Heumann,
  • Özge Kaya,
  • Christoph Burdelski,
  • Claudia Hube-Magg,
  • Martina Kluth,
  • Dagmar S. Lang,
  • Ronald Simon,
  • Burkhard Beyer,
  • Imke Thederan,
  • Guido Sauter,
  • Jakob R. Izbicki,
  • Andreas M. Luebke,
  • Andrea Hinsch,
  • Frank Jacobsen,
  • Corinna Wittmer,
  • Franziska Büscheck,
  • Doris Höflmayer,
  • Sarah Minner,
  • Maria Christina Tsourlakis,
  • Thorsten Schlomm,
  • Waldemar Wilczak

DOI
https://doi.org/10.1038/s41598-017-02279-x
Journal volume & issue
Vol. 7, no. 1
pp. 1 – 10

Abstract

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Abstract Y-box binding protein 1 (YB-1) is an RNA and DNA binding factor with potential prognostic cancer. To evaluate the clinical impact of YB-1, a tissue microarray with 11,152 prostate cancers was analysed by immunohistochemistry. Cytoplasmic and nuclear staining was separately analysed. Cytoplasmic YB-1 was absent or weak in normal epithelium but seen in 86,3% of carcinomas. Cytoplasmic staining was weak, moderate, and strong in 29.6%, 43.7% and 13.0% of tumours and was accompanied by nuclear YB-1 staining in 32.1% of cases. Particularly nuclear staining was strongly linked to poor patient prognosis (p < 0.0001). YB-1 protein was more abundant in ERG positive (95.1%) than in ERG negative cancers (80.4%; p < 0.0001), but any prognostic impact of YB-1 staining was limited to the ERG-negative subset. Similarly, significant associations with pT stage and Gleason grade (p < 0.0001 each) were driven by the ERG negative subset. The significant association of YB-1 protein detection with deletions of PTEN, 5q21 and 6q15 fits well in the protein’s role as an inhibitor of DNA damage dependent cell cycle arrest, a role that is likely to induce genomic instability. In summary, the data show, that the prognostic impact of YB-1 expression is limited to ERG negative prostate cancers.