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Phosphorylation Status of Fas-associated Death Domain Protein Is Associated With Biochemical Recurrence After Radical Prostatectomy

Authors :
Ikeda, Tomohiro
Tanaka, Nobumichi
Shimada, Keiji
Matsumura, Yoshiaki
Miyake, Makito
Anai, Satoshi
Tomioka, Atsushi
Okajima, Eijiro
Hirayama, Akihide
Fujimoto, Kiyohide
Konishi, Noboru
Hirao, Yoshihiko
Source :
Urology. Mar2013, Vol. 81 Issue 3, p607-610. 4p.
Publication Year :
2013

Abstract

Objective: To assess whether the phosphorylated Fas-associated death domain protein (FADD) at 194 serine (p-FADD) is valuable as a marker of biochemical recurrence in hormone-naive patients who had undergone radical prostatectomy. Materials and Methods: We used radical prostatectomy specimens from 106 patients. None of the patients had received neoadjuvant or adjuvant therapy. The percentage of positive p-FADD cells (nuclear staining) was immunohistochemically evaluated. The correlation between FADD phosphorylation and the clinicopathologic parameters was assessed. The correlation between the biochemical recurrence-free rate and the p-FADD expression level was analyzed using the Kaplan-Meier method. Results: Overall, 39 patients developed biochemical recurrence. We investigated the expression of p-FADD in 106 patients with prostate cancer using immunohistochemistry. We compared our findings with the clinicopathologic parameters, including the follow-up data. Patients with a greater positive p-FADD rate had a significantly lower biochemical recurrence rate than those with a lower positive p-FADD rate (P < .001). A significant inverse correlation was found between the positive p-FADD rate and the Gleason score. Conclusion: A low expression of p-FADD could be a predictor of biochemical recurrence in hormone-naive patients who have undergone radical prostatectomy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00904295
Volume :
81
Issue :
3
Database :
Academic Search Index
Journal :
Urology
Publication Type :
Academic Journal
Accession number :
85813842
Full Text :
https://doi.org/10.1016/j.urology.2012.11.032