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http://purl.uniprot.org/citations/28107606http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/28107606http://www.w3.org/2000/01/rdf-schema#comment"

Objective

To identify new biomarkers for biochemical recurrence (BCR) of prostate adenocarcinoma.

Patients and methods

Clinical information of 500 patients with prostate adenocarcinoma and their 152 RNA-sequencing and protein-array data from The Cancer Genome Atlas (TCGA) were separated into a discovery set and a validation set. Each dataset was analysed according to the Gleason grade groups reflecting BCR. The results obtained from the analysis using TCGA dataset were confirmed by immunohistochemistry analyses of a confirmation cohort composed of 395 patients with localised prostate adenocarcinoma.

Results

TCGA discovery set was subgrouped into lower- and higher-risk groups for recurrence-free survival (RFS) (P < 0.001). Cyclin B1 (CCNB1), dishevelled segment polarity protein 3 (DVL3), paxillin (PXN), RAF1, transferrin, X-ray repair cross complementing 5 (XRCC5) and BIM had lower expression in the lower-risk group than that in the higher-risk group (all, P < 0.05). In TCGA validation set, CCNB1, DVL3, transferrin, XRCC5 and BIM were also differently expressed between the two groups. Immunohistochemically, DVL3 positivity was associated with high prostate-specific antigen (PSA) levels, resection margin involvement, and BCR (all, P < 0.05). A high Gleason score indicated a marginal relationship (P = 0.055). BIM positivity was related to high PSA levels, lymphovascular invasion, and BCR (all, P < 0.05). Both DVL3 positivity (P = 0.010) and BIM positivity (P = 0.024) were associated with shorter RFS, but statistical significance was lost when the multivariate Cox regression model included all patients. In the lower-risk group, the multivariate Cox model confirmed that DVL3 was an independent predictor for poor RFS (hazard ratio 1.80, P = 0.040), and the concordance index (C-index) was 0.805.

Conclusions

DVL3 and BIM were expressed in patients with a higher risk of BCR. DVL3 may be a novel and easily applicable recurrence predictor of localised prostate adenocarcinoma."xsd:string
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http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/author"Kim H.G."xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/author"Park J.Y."xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/author"Kim P.J."xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/author"Go H."xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/author"Cho Y.M."xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/date"2017"xsd:gYear
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/name"BJU Int"xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/pages"343-350"xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/title"Dishevelled segment polarity protein 3 (DVL3): a novel and easily applicable recurrence predictor in localised prostate adenocarcinoma."xsd:string
http://purl.uniprot.org/citations/28107606http://purl.uniprot.org/core/volume"120"xsd:string
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