dc.contributor.author | Andersen, Sigve | |
dc.contributor.author | Richardsen, Elin | |
dc.contributor.author | Rakaee, Mehrdad | |
dc.contributor.author | Bertilsson, Helena | |
dc.contributor.author | Bremnes, Roy | |
dc.contributor.author | Børset, Magne | |
dc.contributor.author | Busund, Lill-Tove | |
dc.contributor.author | Slørdahl, Tobias | |
dc.date.accessioned | 2018-01-09T08:19:02Z | |
dc.date.available | 2018-01-09T08:19:02Z | |
dc.date.issued | 2017-11-30 | |
dc.description.abstract | Background:
Prostate cancer (PC) stratification needs new prognostic tools to reduce overtreatment. Phosphatase of regenerating liver (PRL-3) is a phosphatase found at high levels in several cancer types, where its expression is associated with survival. A recent PC cell line study has shown it to be involved in PC growth and migration.
<br>Methods:
We used a monoclonal antibody to evaluate the expression of PRL-3 in PC tissue of patients in an unselected cohort of 535 prostatectomy patients. We analyzed associations between PRL-3 expression and biochemical failure-free survival (BFFS), clinical failure-free survival (CFFS) and PC death-free survival (PCDFS).
<br>Results:
Cytoplasmic PRL-3 staining in tumor cells was significantly correlated to expression of molecules in the VEGFR-axis, but not to the clinicopathological variables. High PRL-3 was not significantly associated with survival in the univariate analysis for BFFS (p = 0.131), but significantly associated with CFFS (p = 0.044) and PCDFS (p = 0.041). In multivariate analysis for the various end points, PRL-3 came out as an independent and significant indicator of poor survival for BFFS (HR = 1.53, CI95% 1.10–2.13, p = 0.012), CFFS (HR = 2.41, CI95% 1.17–4.98, p = 0.017) and PCDFS (HR = 3.99, CI95% 1.21–13.1, p = 0.023).
<br>Conclusions:
PRL-3 is independently associated with all PC endpoints in this study. Since high PRL-3 expression also correlates with poor prognosis in other cancers and functional studies in PC support these findings, PRL-3 emerges as a potential treatment target in PC. | en_US |
dc.description | Source at <a href=https://doi.org/10.1371/journal.pone.0189000> https://doi.org/10.1371/journal.pone.0189000 </a> | en_US |
dc.identifier.citation | Andersen S, Richardsen E, Rakaee M, Bertilsson H, Bremnes R, Børset M, Busund L-T, Slørdahl T. (2017) Expression of phosphatase of regenerating liver (PRL)-3, is independently associated with biochemical failure, clinical failure and death in prostate cancer. PLoS ONE 12(11): e0189000. | en_US |
dc.identifier.cristinID | FRIDAID 1519289 | |
dc.identifier.doi | 10.1371/journal.pone.0189000 | |
dc.identifier.issn | 1932-6203 | |
dc.identifier.uri | https://hdl.handle.net/10037/11936 | |
dc.language.iso | eng | en_US |
dc.publisher | Public Library of Science | en_US |
dc.relation.journal | PLoS ONE | |
dc.rights.accessRights | openAccess | en_US |
dc.subject | VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Onkologi: 762 | en_US |
dc.subject | VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Oncology: 762 | en_US |
dc.title | Expression of phosphatase of regenerating liver (PRL)-3, is independently associated with biochemical failure, clinical failure and death in prostate cancer | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |