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   <subfield code="a">Nutritional supplements, COX - 2 and IGF - 1 expression in men on active surveillance for prostate cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[June Chan, Vivian Weinberg, Mark Magbanua, Eduardo Sosa, Jeffry Simko, Katsuto Shinohara, Scot Federman, Mike Mattie, Millie Hughes-Fulford, Christopher Haqq, Peter Carroll]</subfield>
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   <subfield code="a">Background: Nutritional factors are associated with reduced risk of prostate cancer progression, yet mechanisms remain unclear. We examined the effects of lycopene and fish oil supplements versus placebo on the normal prostate microenvironment, among men pursuing active surveillance for low-burden prostate cancer. We hypothesized that lycopene or fish oil supplements would down-regulate insulin-like growth factor-1 (IGF-1) and cyclooxygenase 2 (COX-2) gene expression, respectively, reflecting putative proliferation (IGF-1) and inflammatory (COX-2) pathways relevant to carcinogenesis. Methods: We conducted a 3-month randomized, double-blinded, clinical trial comparing prostate tissue gene expression profiles (assessed by qRT-PCR) among men with favorable-risk prostate cancer receiving either 30mg/day lycopene, 3g/day fish oil (including 1,098mg eicosapentaenoic and 549mg docosahexaenoic fatty acids) or placebo. Results: Among 69 men (22 assigned to lycopene, 21 to fish, and 26 to placebo), there was no difference in the change from baseline to the 3 months in IGF-1 expression level between the placebo and lycopene arms (p=0.93) nor in COX-2 expression between the placebo and fish arms (p=0.99). Conclusion: Compared to placebo, 3-month intervention with lycopene or fish oil did not significantly change IGF-1 and COX-2 gene expression in the normal prostate microenvironment in men with low-burden prostate cancer. Further analysis of global gene expression profiles may shed light on the bioactivity and relevance of these nutrients in prostate cancer.</subfield>
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   <subfield code="a">The Author(s), 2010</subfield>
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   <subfield code="a">Prostate cancer</subfield>
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   <subfield code="u">Department of Urology, University of California San Francisco (UCSF), MC 3110, 1450 3rd Street, PO Box 589001, 94158-9001, San Francisco, CA, USA</subfield>
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   <subfield code="a">Weinberg</subfield>
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   <subfield code="u">Helen Diller Family Comprehensive Cancer Center Biostatistics Core, UCSF, San Francisco, USA</subfield>
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   <subfield code="a">Magbanua</subfield>
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   <subfield code="u">Helen Diller Family Comprehensive Cancer Center, UCSF, San Francisco, USA</subfield>
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