Increased levels of plasma haemoxygenase-1 in prostate cancer
Angiogenesis, a key component of cancer, may be driven by angiogenic growth factors, such as vascular endothelial growth factor (VEGF) and angiopoietin-2. Haemoxygenase-1 (HO-1), a haem-degrading enzyme, may have alternative roles in angiogenesis. Levels of plasma HO-1 have not been reported in pros...
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Published in | Prostate cancer and prostatic diseases Vol. 14; no. 2; pp. 114 - 117 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.06.2011
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1365-7852 1476-5608 1476-5608 |
DOI | 10.1038/pcan.2010.56 |
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Summary: | Angiogenesis, a key component of cancer, may be driven by angiogenic growth factors, such as vascular endothelial growth factor (VEGF) and angiopoietin-2. Haemoxygenase-1 (HO-1), a haem-degrading enzyme, may have alternative roles in angiogenesis. Levels of plasma HO-1 have not been reported in prostate cancer. We tested the hypothesis of abnormal HO-1 in 30 men with early prostate cancer, compared with 22 men with benign prostate disease (BPD) and 26 men free of prostate disease, and that HO-1 levels would correlate with VEGF, angiopoietin-2, von Willebrand factor (vWf, marking endothelial perturbation) and PSA. Plasma HO-1 was twofold higher in prostate cancer than in the two control groups, while vWf, VEGF and PSA were also raised (all
P
<0.02). In the subjects free of prostate disease and in the BPD groups, HO-1 correlated significantly with VEGF (
r
>0.5,
P
<0.02) but the correlation in prostate cancer was not significant (
r
=0.117,
P
=0.537). There were no correlations with PSA or the Gleason stage. We conclude that HO-1 is associated with VEGF in health and BPD, but in the presence of prostate cancer, raised levels of both HO-1 and VEGF fail to correlate. This observation may have implications for the pathogenesis of prostate cancer. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1365-7852 1476-5608 1476-5608 |
DOI: | 10.1038/pcan.2010.56 |