作者: Okyaz Eminaga , Wei Wei , Sarah J. Hawley , Heidi Auman , Lisa F. Newcomb
DOI: 10.1371/JOURNAL.PONE.0165236
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摘要: Author(s): Eminaga, Okyaz; Wei, Wei; Hawley, Sarah J; Auman, Heidi; Newcomb, Lisa F; Simko, Jeff; Hurtado-Coll, Antonio; Troyer, Dean A; Carroll, Peter R; Gleave, Martin E; Lin, Daniel W; Nelson, S; Thompson, Ian M; True, Lawrence D; McKenney, Jesse K; Feng, Ziding; Fazli, Ladan; Brooks, James D | Abstract: BackgroundThe uncertainties inherent in clinical measures of prostate cancer (CaP) aggressiveness endorse the investigation clinically validated tissue biomarkers. MUC1 expression has been previously reported to independently predict aggressive localized cancer. We used a large cohort validate whether protein levels measured by immunohistochemistry (IHC) cancer, recurrence and survival outcomes after radical prostatectomy independent pathological parameters.Material methodsMUC1 IHC was performed on multi-institutional microarray (TMA) resource including 1,326 men with median follow-up 5 years. Associations parameters were tested Chi-square test Wilcoxon rank sum test. Relationships outcome assessed univariable multivariable Cox proportional hazard models Log-rank test.ResultsThe presence significantly associated extracapsular extension higher Gleason score, but not seminal vesicle invasion, age, positive surgical margins or pre-operative serum PSA levels. In analyses, staining worse free (RFS) (HR: 1.24, CI 1.03-1.49, P = 0.02), although disease specific (DSS, Pg0.5). On margins, extension, as well increasing score RFS, while not. Positive (DSS), weakly overall (OS).ConclusionIn our large, rigorously designed validation cohort, adverse features, it an predictor prostatectomy.