1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1

<p>Abstract</p> <p>Background</p> <p>Prostate cancer is the second leading cause of cancer mortality among US men. Epidemiological evidence suggests that high vitamin D status protects men from prostate cancer and the active form of vitamin D, 1α,25 dihydroxyvitamin D&l...

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Main Authors: Clinton Steve K, Cui Min, Zhang Zhentao, Kovalenko Pavlo L, Fleet James C
Format: Article
Language:English
Published: BMC 2010-01-01
Series:BMC Genomics
Online Access:http://www.biomedcentral.com/1471-2164/11/26
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spelling doaj-2cb2daa5b33e4c688534422f8d180a452020-11-25T00:58:03ZengBMCBMC Genomics1471-21642010-01-011112610.1186/1471-2164-11-261,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1Clinton Steve KCui MinZhang ZhentaoKovalenko Pavlo LFleet James C<p>Abstract</p> <p>Background</p> <p>Prostate cancer is the second leading cause of cancer mortality among US men. Epidemiological evidence suggests that high vitamin D status protects men from prostate cancer and the active form of vitamin D, 1α,25 dihydroxyvitamin D<sub>3 </sub>(1,25(OH)<sub>2</sub>D) has anti-cancer effects in cultured prostate cells. Still, the molecular mechanisms and the gene targets for vitamin D-mediated prostate cancer prevention are unknown.</p> <p>Results</p> <p>We examined the effect of 1,25(OH)<sub>2</sub>D (+/- 100 nM, 6, 24, 48 h) on the transcript profile of proliferating RWPE1 cells, an immortalized, non-tumorigenic prostate epithelial cell line that is growth arrested by 1,25(OH)<sub>2</sub>D (Affymetrix U133 Plus 2.0, n = 4/treatment per time and dose). Our analysis revealed many transcript level changes at a 5% false detection rate: 6 h, 1571 (61% up), 24 h, 1816 (60% up), 48 h, 3566 (38% up). 288 transcripts were regulated similarly at all time points (182 up, 80 down) and many of the promoters for these transcripts contained putative vitamin D response elements. Functional analysis by pathway or Gene Set Analysis revealed early suppression of WNT, Notch, NF-kB, and IGF1 signaling. Transcripts related to inflammation were suppressed at 6 h (e.g. IL-1 pathway) and suppression of proinflammatory pathways continued at later time points (e.g. IL-17 and IL-6 pathways). There was also evidence for induction of anti-angiogenic pathways and induction of transcripts for protection from oxidative stress or maintenance of cell redox homeostasis at 6 h.</p> <p>Conclusions</p> <p>Our data reveal of large number of potential new, direct vitamin D target genes relevant to prostate cancer prevention. In addition, our data suggests that rather than having a single strong regulatory effect, vitamin D orchestrates a pattern of changes within prostate epithelial cells that limit or slow carcinogenesis.</p> http://www.biomedcentral.com/1471-2164/11/26
collection DOAJ
language English
format Article
sources DOAJ
author Clinton Steve K
Cui Min
Zhang Zhentao
Kovalenko Pavlo L
Fleet James C
spellingShingle Clinton Steve K
Cui Min
Zhang Zhentao
Kovalenko Pavlo L
Fleet James C
1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1
BMC Genomics
author_facet Clinton Steve K
Cui Min
Zhang Zhentao
Kovalenko Pavlo L
Fleet James C
author_sort Clinton Steve K
title 1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1
title_short 1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1
title_full 1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1
title_fullStr 1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1
title_full_unstemmed 1,25 dihydroxyvitamin D-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, RWPE1
title_sort 1,25 dihydroxyvitamin d-mediated orchestration of anticancer, transcript-level effects in the immortalized, non-transformed prostate epithelial cell line, rwpe1
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2010-01-01
description <p>Abstract</p> <p>Background</p> <p>Prostate cancer is the second leading cause of cancer mortality among US men. Epidemiological evidence suggests that high vitamin D status protects men from prostate cancer and the active form of vitamin D, 1α,25 dihydroxyvitamin D<sub>3 </sub>(1,25(OH)<sub>2</sub>D) has anti-cancer effects in cultured prostate cells. Still, the molecular mechanisms and the gene targets for vitamin D-mediated prostate cancer prevention are unknown.</p> <p>Results</p> <p>We examined the effect of 1,25(OH)<sub>2</sub>D (+/- 100 nM, 6, 24, 48 h) on the transcript profile of proliferating RWPE1 cells, an immortalized, non-tumorigenic prostate epithelial cell line that is growth arrested by 1,25(OH)<sub>2</sub>D (Affymetrix U133 Plus 2.0, n = 4/treatment per time and dose). Our analysis revealed many transcript level changes at a 5% false detection rate: 6 h, 1571 (61% up), 24 h, 1816 (60% up), 48 h, 3566 (38% up). 288 transcripts were regulated similarly at all time points (182 up, 80 down) and many of the promoters for these transcripts contained putative vitamin D response elements. Functional analysis by pathway or Gene Set Analysis revealed early suppression of WNT, Notch, NF-kB, and IGF1 signaling. Transcripts related to inflammation were suppressed at 6 h (e.g. IL-1 pathway) and suppression of proinflammatory pathways continued at later time points (e.g. IL-17 and IL-6 pathways). There was also evidence for induction of anti-angiogenic pathways and induction of transcripts for protection from oxidative stress or maintenance of cell redox homeostasis at 6 h.</p> <p>Conclusions</p> <p>Our data reveal of large number of potential new, direct vitamin D target genes relevant to prostate cancer prevention. In addition, our data suggests that rather than having a single strong regulatory effect, vitamin D orchestrates a pattern of changes within prostate epithelial cells that limit or slow carcinogenesis.</p>
url http://www.biomedcentral.com/1471-2164/11/26
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