The Androgen Receptor Is Significantly Associated with Vascular Endothelial Growth Factor and Hypoxia Sensing via Hypoxia-Inducible Factors HIF-1a, HIF-2a, and the Prolyl Hydroxylases in Human Prostate Cancer

Purpose: Hypoxia regulates key biological processes including angiogenesis via the transcription factor, hypoxia-inducible factor (HIF). In prostate cancer, angiogenesis is also influenced by androgens, and recent cell line studies suggest that this effect is partly mediated by HIF. The study aimed...

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Published in:	Clinical cancer research Vol. 11; no. 21; pp. 7658 - 7663
Main Authors:	BEADY, Jane L, FOX, Stephen B, CHENG HAN, CAMPO, Leticia, TURLEY, Helen, KANGA, Suresh, MALONE, Peter R, HARRIS, Adrian L
Format:	Journal Article
Language:	English
Published:	Philadelphia, PA American Association for Cancer Research 01-11-2005
Subjects:	Aged Androgens Angiogenesis Antineoplastic agents Basic Helix-Loop-Helix Transcription Factors - biosynthesis Biological and medical sciences Disease Progression Disease-Free Survival Gene Expression Regulation, Neoplastic Gynecology. Andrology. Obstetrics Humans Hypoxia Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis Immunohistochemistry Male Male genital diseases Medical sciences Middle Aged Models, Statistical Neovascularization, Pathologic Nephrology. Urinary tract diseases Pharmacology. Drug treatments Procollagen-Proline Dioxygenase - biosynthesis Proportional Hazards Models Prostate-Specific Antigen - biosynthesis Prostatic Neoplasms - metabolism Prostatic Neoplasms - pathology Receptors, Androgen - biosynthesis Recurrence Tumors Tumors of the urinary system Urinary tract. Prostate gland Vascular Endothelial Growth Factor A - biosynthesis Vascular Endothelial Growth Factor A - metabolism Human Oxygen Urinary system disease Prostate disease Enzyme Hydroxylase Malignant tumor Vascular endothelium growth factor Androgen receptor Hypoxia Oxidoreductases Male genital diseases Prostate cancer Hormonal receptor
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Summary:	Purpose: Hypoxia regulates key biological processes including angiogenesis via the transcription factor, hypoxia-inducible factor (HIF). In prostate cancer, angiogenesis is also influenced by androgens, and recent cell line studies suggest that this effect is partly mediated by HIF. The study aimed to assess whether a relationship exists in human prostate cancer between expression of the androgen receptor, HIFs, and the key angiogenesis factor, vascular endothelial growth factor (VEGF). Experimental Design: A tissue microarray comprised of 149 radical prostatectomy specimens was constructed. Semiquantitative immunohistochemical analysis was used to assess the expression of the androgen receptor, VEGF and HIF-1a and 2a, and their regulatory prolyl hydroxylase enzymes (PHD1, PHD2, and PHD3). Statistical analysis compared these factors with each other and with prostate-specific antigen relapse. Results: There was a significant correlation between HIF-1a and HIF-2a expression ( P = 0.02), and with androgen receptor ( P = 0.04 and P < 0.001, respectively) and VEGF expression ( P = 0.05 and P < 0.001, respectively). VEGF was also significantly related to the androgen receptor ( P = 0.05), whereas PHD2 was inversely related to HIF-2a expression. No significant association was shown between HIF-1a or HIF-2a and time to prostate-specific antigen recurrence ( P = 0.20 and P = 0.94, respectively). Conclusions: These findings confirm the relationship between hypoxia and the androgen receptor in prostate cancer, and show for the first time, the role of HIF-2a in this disease process. They provide clinical evidence to support the recent cell line findings that androgens may regulate VEGF levels through the activation of HIF in androgen-sensitive tumors. Inhibition of both the HIF pathways may provide new therapeutic options in the management of this disease.
Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	1078-0432 1557-3265
DOI:	10.1158/1078-0432.CCR-05-0460