4.1 Article

Nuclear ubiquitin C-terminal hydrolase L5 expression associates with increased patient survival in pancreatic ductal adenocarcinoma

Journal

TUMOR BIOLOGY
Volume 39, Issue 6, Pages -

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/1010428317710411

Keywords

Deubiquitination; pancreatic ductal adenocarcinoma; prognosis; proteasome; ubiquitin C-terminal hydrolase L5; UCHL5

Categories

Funding

  1. Academy of Finland [259797, 297776]
  2. Medicinska Understodsforeningen Liv och Halsa r.f.
  3. Ruth and Nils-Erik Stenback Foundation
  4. Sigrid Juselius Foundation
  5. Cancer Society of Finland
  6. Mary and Georg C Ehrnrooth Foundation
  7. Helsinki University Hospital Research Fund
  8. Doctoral Programme in Biomedicine, University of Helsinki
  9. Victoria Foundation
  10. K. Albin Johansson Foundation
  11. Ida Montin Foundation
  12. Academy of Finland (AKA) [297776, 259797, 297776, 259797] Funding Source: Academy of Finland (AKA)

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Pancreatic ductal adenocarcinoma is a lethal disease with an overall 5-year survival of less than 5%. Prognosis among surgically treated patients is difficult and identification of new biomarkers is essential for accurate prediction of patient outcome. As part of one of the major cellular protein degradation systems, the proteasome plays a fundamental role in both physiological and pathophysiological conditions including cancer. The proteasome-associated deubiquitinating enzyme ubiquitin C-terminal hydrolase L5 (UCHL5)/Uch37 is a modulator of proteasome activity with cancer prognostic marker potential. Cytoplasmic and nuclear immunoexpression of UCHL5 was evaluated in 154 surgical specimens from pancreatic ductal adenocarcinoma patients treated at Helsinki University Hospital, Finland, in 2000-2011. UCHL5 expression in relation to clinicopathological parameters and the association between UCHL5 In this study, positive expression and patient survival were assessed. Positive nuclear UCHL5 expression was associated with increased patient survival (p = 0.005). A survival benefit was also detectable in these subgroups of patients: over 65 years (p < 0.001), at tumor stages IIB to III (p = 0.007), or with lymph-node positivity (p = 0.006). In stages IIB to III disease, patients with positive nuclear UCHL5 expression showed a twofold increase in 5-year cancer-specific survival compared to those with negative expression. Multivariate analysis identified positive nuclear UCHL5 expression as an independent prognostic factor (p = 0.012). In conclusion, UCHL5 expression could function as a prognostic marker in pancreatic ductal adenocarcinoma, particularly at disease stages IIB to III. As UCHL5 is one of the few markers predicting increased survival, our results may be of clinical relevance.

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