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Loss of cytoplasmic survivin expression is an independent predictor of poor prognosis in radically operated prostate cancer patients.
Büscheck, Franziska; Sulimankhil, Mariam; Melling, Nathaniel; Höflmayer, Doris; Hube-Magg, Claudia; Simon, Ronald; Göbel, Cosima; Hinsch, Andrea; Weidemann, Sören; Izbicki, Jacob R; Jacobsen, Frank; Mandelkow, Tim; Blessin, Niclas C; Möller-Koop, Christina; Lutz, Florian; Viehweger, Florian; Möller, Katharina; Sauter, Guido; Lennartz, Maximillian; Burandt, Eike; Lebok, Patrick; Minner, Sarah; Bonk, Sarah; Huland, Hartwig; Graefen, Markus; Schlomm, Thorsten; Fraune, Christoph.
Affiliation
  • Büscheck F; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Sulimankhil M; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Melling N; General, Visceral and Thoracic Surgery Department and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Höflmayer D; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Hube-Magg C; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Simon R; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Göbel C; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Hinsch A; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Weidemann S; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Izbicki JR; General, Visceral and Thoracic Surgery Department and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Jacobsen F; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Mandelkow T; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Blessin NC; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Möller-Koop C; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Lutz F; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Viehweger F; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Möller K; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Sauter G; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Lennartz M; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Burandt E; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Lebok P; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Minner S; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Bonk S; General, Visceral and Thoracic Surgery Department and Clinic, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Huland H; Martini-Clinic, Prostate Cancer Center, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Graefen M; Martini-Clinic, Prostate Cancer Center, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Schlomm T; Department of Urology, Charité-University Medical Center Berlin, Berlin, Germany.
  • Fraune C; Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Cancer Med ; 9(4): 1409-1418, 2020 02.
Article in En | MEDLINE | ID: mdl-31893572
ABSTRACT
Survivin is an inhibitor of apoptosis. Aberrant survivin expression occurs in malignant tumors and has often been linked to unfavorable patient outcome. Here we analyzed 12 432 prostate cancers by immunohistochemistry. Survivin immunostaining was regularly expressed at high levels in normal prostate epithelium but expression was often reduced in prostate cancers. Among 9492 evaluable prostate cancers, 9% expressed survivin strongly, 19% moderately, 28% weakly, and 44% lacked it. Loss of cytoplasmic survivin was seen in advanced tumor stage, higher Gleason score, preoperative PSA levels, and Ki-67 labeling index, and associated with earlier PSA recurrence (P < .0001). Survivin loss was significantly more common in cancers carrying TMPRSS2ERG fusions (61% survivin negative) than in ERG wild-type cancers (32% survivin negative; P < .0001). Multivariate analysis revealed that reduced cytoplasmic survivin expression predicted poor prognosis independent from Gleason score, pT, pN, and serum PSA level. This was valid for ERG-positive and ERG-negative cancers. Survivin expression loss even retained its prognostic impact in 1020 PTEN deleted cancers, a group that is already characterized by dismal patient prognosis. In conclusion, reduced survivin expression is associated with more aggressive tumors and inferior prognosis in prostate cancer.
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Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Prostate / Prostatectomy / Prostatic Neoplasms / Biomarkers, Tumor / Survivin Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: Cancer Med Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Prostate / Prostatectomy / Prostatic Neoplasms / Biomarkers, Tumor / Survivin Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Aged / Humans / Male / Middle aged Language: En Journal: Cancer Med Year: 2020 Document type: Article