4.4 Article

Decreased stromal expression and increased epithelial expression of WFDCI/ps20 in prostate cancer is associated with reduced recurrence-free survival

期刊

PROSTATE
卷 61, 期 2, 页码 182-191

出版社

WILEY
DOI: 10.1002/pros.20085

关键词

WAP domain; reactive stroma; biomarkers; prostate cancer

资金

  1. NCI NIH HHS [CA58204, R01-CA58093, U01-CA84296] Funding Source: Medline
  2. NIDDK NIH HHS [R01-DK45909] Funding Source: Medline

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BACKGROUND. WAP-type four disulfide core (WFDC1)/ps20 is a member of the whey acidic protein family, which includes several serine protease inhibitors. Expression of WFDC1/ps20 was previously demonstrated in the normal human prostate stromal compartment. To further current understanding of the role of WFDC1 /ps20 in prostate cancer, altered expression of WFDC1/p20 protein in prostate cancer was evaluated. METHODS. Immunohistochemical staining for WFDC1/ps20 was performed using tissue microarrays. Quantitation was based on the percentage of positive-staining stromal or epithelial cells and staining intensity. Resulting data was analyzed relative to the recurrence-free survival data and additional information for this patient set. RESULTS. Decreased stromal expression of WFDC1/ps20 predicted shorter recurrence-free survival time by univariate analysis. Decreased stromal WFDC1/ps20 expression correlated with higher radical prostatectomy Gleason scores, positive surgical margins, extracapsular extension, higher clinical stage, and higher preoperative prostate specific antigen levels. Increased epithelial expression of WFDC1/ps20 also predicted shorter recurrence-free survival times by univariate analysis. Increased epithelial expression of WFDC1/ps20 correlated with higher biopsy and radical prostatectomy Gleason scores, and higher clinical stage. CONCLUSIONS. Decreased stromal WFDC1/ps20 expression reflects the evolution of a prostate cancer reactive stroma, while increased epithelial WFDC1/ps20 expression may indicate progression to a more aggressive epithelial phenotype and may indicate an epithelial mesenchymal transition (EMT) process. Further evaluation of WFDC1/ps20 biologic functions will aid in the understanding of this interesting expression profile. (C) 2004 Wiley-Liss, Inc.

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