TY - JOUR
T1 - The prognostic significance of vasohibin-1 expression in patients with prostate cancer
AU - Kosaka, T.
AU - Miyazaki, Y.
AU - Miyajima, Akira
AU - Mikami, Shuji
AU - Hayashi, Yuichiro
AU - Tanaka, N.
AU - Nagata, H.
AU - Kikuchi, Eiji
AU - Nakagawa, K.
AU - Okada, Yasunori
AU - Sato, Y.
AU - Oya, M.
N1 - Funding Information:
We thank colleagues from the Department of Vascular Biology, Institute of Development, Aging and Cancer, Tohoku University for their excellent technical assistance in purifying anti-human VASH1 mAb. This work was supported in part by grants-in-aid for Scientific Research from the Ministry of Education, Culture, Sports, Science, and Technology of Japan, by the Prostate Research Fund in Japan, the Japan Urological Association (5th Young Research Grant 2011 to TK) and the Cooperative Research Project Program 2011, 2012 of Joint Usage/Research Center at the Institute of Development, Aging and Cancer, Tohoku University.
PY - 2013/5
Y1 - 2013/5
N2 - 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 mm 2) and 89.1% in patients with lower VASH1 density (<12 per mm 2), 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.
AB - 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 mm 2) and 89.1% in patients with lower VASH1 density (<12 per mm 2), 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.
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U2 - 10.1038/bjc.2013.169
DO - 10.1038/bjc.2013.169
M3 - Article
C2 - 23591203
AN - SCOPUS:84878533977
SN - 0007-0920
VL - 108
SP - 2123
EP - 2129
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 10
ER -