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The prognostic significance of vasohibin-1 expression in patients with prostate cancer.

Authors :
Kosaka, T
Miyazaki, Y
Miyajima, A
Mikami, S
Hayashi, Y
Tanaka, N
Nagata, H
Kikuchi, E
Nakagawa, K
Okada, Y
Sato, Y
Oya, M
Source :
British Journal of Cancer. 5/21/2013, Vol. 108 Issue 10, p2123-2129. 7p. 1 Black and White Photograph, 3 Charts, 2 Graphs.
Publication Year :
2013

Abstract

Background:We recently isolated vasohibin-1 (VASH1), a novel angiogenic molecule that is specifically expressed in activated vascular endothelial cells (ECs), and the status of VASH1 expression has been documented in various cancer angiogenesis. The aim of this study was to assess the prognostic value of VASH1 expression in prostate cancer (PCa).Methods:In this study, we retrospectively analysed the clinical records and evaluated the VASH1 expression of tumour microvessels in 167 patients with PCa who underwent radical prostatectomy. We immunohistochemically examined the microvessels positive for anti-CD34 as microvessel density (MVD) and the microvessels with activated ECs positive for VASH1 density.Results:We found that the VASH1 expression was restricted to ECs in the tumour stroma. VASH1 density was significantly associated with pathological T stage, Gleason score and MVD. The 5-year PSA recurrence-free survival rate was 58.8% in patients with higher VASH1 density (≧12 per mm2) and 89.1% in patients with lower VASH1 density (<12 per mm2), respectively (P<0.001). Microvessel density was not an independent predictor of PSA recurrence. Multivariate analysis revealed that high VASH1 density was an independent prognostic indicator of PSA recurrence (P=0.007, HR=2.950).Conclusion:VASH1 density represents a clinically relevant predictor of patient prognosis and can be a new biomarker that would provide additional prognostic information in PCa. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
108
Issue :
10
Database :
Academic Search Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
87797468
Full Text :
https://doi.org/10.1038/bjc.2013.169