An expression signature at diagnosis to estimate prostate cancer patients’ overall survival

Background: This study aimed to identify biomarkers for estimating the overall and prostate cancer (PCa)-specific survival in PCa patients at diagnosis. Methods: To explore the importance of embryonic stem cell (ESC) gene signatures, we identified 641 ESC gene predictors (ESCGPs) using published mic...

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Veröffentlicht in:Prostate cancer and prostatic diseases 2014-03, Vol.17 (1), p.81-90
Hauptverfasser: Peng, Z, Skoog, L, Hellborg, H, Jonstam, G, Wingmo, I-L, Hjälm-Eriksson, M, Harmenberg, U, Cedermark, G C, Andersson, K, Ährlund-Richter, L, Pramana, S, Pawitan, Y, Nistér, M, Nilsson, S, Li, C
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Sprache:eng
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Zusammenfassung:Background: This study aimed to identify biomarkers for estimating the overall and prostate cancer (PCa)-specific survival in PCa patients at diagnosis. Methods: To explore the importance of embryonic stem cell (ESC) gene signatures, we identified 641 ESC gene predictors (ESCGPs) using published microarray data sets. ESCGPs were selected in a stepwise manner, and were combined with reported genes. Selected genes were analyzed by multiplex quantitative polymerase chain reaction using prostate fine-needle aspiration samples taken at diagnosis from a Swedish cohort of 189 PCa patients diagnosed between 1986 and 2001. Of these patients, there was overall and PCa-specific survival data available for 97.9%, and 77.9% were primarily treated by hormone therapy only. Univariate and multivariate Cox proportional hazard ratios and Kaplan–Meier plots were used for the survival analysis, and a k -nearest neighbor (kNN) algorithm for estimating overall survival. Results: An expression signature of VGLL3, IGFBP3 and F3 was shown sufficient to categorize the patients into high-, intermediate- and low-risk subtypes. The median overall survival times of the subtypes were 3.23, 4.00 and 9.85 years, respectively. The difference corresponded to hazard ratios of 5.86 (95% confidence interval (CI): 2.91–11.78, P
ISSN:1365-7852
1476-5608
1476-5608
DOI:10.1038/pcan.2013.57