Survivin mediates prostate cell protection by HIF-1α against zinc toxicity

BACKGROUND The prostate contains extremely high concentrations of zinc, but survives and grows without apparent injury. This begs the question as to how prostate cells avoid the toxic effects of zinc. In a previous study, the authors found that; HIF‐1α is expressed concomitantly with the accumulatio...

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Published inThe Prostate Vol. 70; no. 11; pp. 1179 - 1188
Main Authors Yun, Young-Joo, Li, Shan-Hua, Cho, Young-Suk, Park, Jong-Wan, Chun, Yang-Sook
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.08.2010
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Abstract BACKGROUND The prostate contains extremely high concentrations of zinc, but survives and grows without apparent injury. This begs the question as to how prostate cells avoid the toxic effects of zinc. In a previous study, the authors found that; HIF‐1α is expressed concomitantly with the accumulation of zinc in the epithelial cells of normal rat prostates, the zinc ion stabilizes HIF‐1α in prostate cells, and that HIF‐1α protects prostate cells from zinc toxicity. In the present study, the authors addressed the mechanism responsible for the protective effect of HIF‐1α in a high zinc environment. METHODS Immunofluorescent staining, immunoblotting, reverse transcription‐polymerase chain reaction, reporter assay, and cell cycle analysis. RESULTS Survivin was induced by ZnCl2 in a HIF‐1 dependent manner in both DU‐145 and PNT2 prostate cells. Furthermore, HIF‐1 induced survivin expression at the transcriptional level and the induction of survivin was abolished by HIF‐1α knock‐down. In addition, HIF‐1‐dependent survivin overexpression promoted prostrate cell survival and prevented cell arrest in the presence of high zinc concentrations, and si‐survivin transfected cells under zinc rich conditions contained markedly higher levels of cleaved caspase‐9 and PARP than si‐con transfected cells. Finally, survivin expression patterns well matched rat prostate proliferation statuses. CONCLUSION Under zinc rich conditions, prostate epithelial cells HIF‐1‐dependently express survivin, which promotes prostate cell proliferation, and prevents apoptosis and cell cycle arrest. Accordingly, the HIF‐1α‐survivin pathway appears to facilitate prostate cell survival and growth in zinc rich environments, and this pathway could be a therapeutic target for the treatment of prostate hyperplasia. Prostate 70: 1179–1188, 2010. © 2010 Wiley‐Liss, Inc.
AbstractList Abstract BACKGROUND The prostate contains extremely high concentrations of zinc, but survives and grows without apparent injury. This begs the question as to how prostate cells avoid the toxic effects of zinc. In a previous study, the authors found that; HIF‐1α is expressed concomitantly with the accumulation of zinc in the epithelial cells of normal rat prostates, the zinc ion stabilizes HIF‐1α in prostate cells, and that HIF‐1α protects prostate cells from zinc toxicity. In the present study, the authors addressed the mechanism responsible for the protective effect of HIF‐1α in a high zinc environment. METHODS Immunofluorescent staining, immunoblotting, reverse transcription‐polymerase chain reaction, reporter assay, and cell cycle analysis. RESULTS Survivin was induced by ZnCl 2 in a HIF‐1 dependent manner in both DU‐145 and PNT2 prostate cells. Furthermore, HIF‐1 induced survivin expression at the transcriptional level and the induction of survivin was abolished by HIF‐1α knock‐down. In addition, HIF‐1‐dependent survivin overexpression promoted prostrate cell survival and prevented cell arrest in the presence of high zinc concentrations, and si‐survivin transfected cells under zinc rich conditions contained markedly higher levels of cleaved caspase‐9 and PARP than si‐con transfected cells. Finally, survivin expression patterns well matched rat prostate proliferation statuses. CONCLUSION Under zinc rich conditions, prostate epithelial cells HIF‐1‐dependently express survivin, which promotes prostate cell proliferation, and prevents apoptosis and cell cycle arrest. Accordingly, the HIF‐1α‐survivin pathway appears to facilitate prostate cell survival and growth in zinc rich environments, and this pathway could be a therapeutic target for the treatment of prostate hyperplasia. Prostate 70: 1179–1188, 2010. © 2010 Wiley‐Liss, Inc.
BACKGROUND The prostate contains extremely high concentrations of zinc, but survives and grows without apparent injury. This begs the question as to how prostate cells avoid the toxic effects of zinc. In a previous study, the authors found that; HIF‐1α is expressed concomitantly with the accumulation of zinc in the epithelial cells of normal rat prostates, the zinc ion stabilizes HIF‐1α in prostate cells, and that HIF‐1α protects prostate cells from zinc toxicity. In the present study, the authors addressed the mechanism responsible for the protective effect of HIF‐1α in a high zinc environment. METHODS Immunofluorescent staining, immunoblotting, reverse transcription‐polymerase chain reaction, reporter assay, and cell cycle analysis. RESULTS Survivin was induced by ZnCl2 in a HIF‐1 dependent manner in both DU‐145 and PNT2 prostate cells. Furthermore, HIF‐1 induced survivin expression at the transcriptional level and the induction of survivin was abolished by HIF‐1α knock‐down. In addition, HIF‐1‐dependent survivin overexpression promoted prostrate cell survival and prevented cell arrest in the presence of high zinc concentrations, and si‐survivin transfected cells under zinc rich conditions contained markedly higher levels of cleaved caspase‐9 and PARP than si‐con transfected cells. Finally, survivin expression patterns well matched rat prostate proliferation statuses. CONCLUSION Under zinc rich conditions, prostate epithelial cells HIF‐1‐dependently express survivin, which promotes prostate cell proliferation, and prevents apoptosis and cell cycle arrest. Accordingly, the HIF‐1α‐survivin pathway appears to facilitate prostate cell survival and growth in zinc rich environments, and this pathway could be a therapeutic target for the treatment of prostate hyperplasia. Prostate 70: 1179–1188, 2010. © 2010 Wiley‐Liss, Inc.
Author Cho, Young-Suk
Li, Shan-Hua
Chun, Yang-Sook
Yun, Young-Joo
Park, Jong-Wan
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Snippet BACKGROUND The prostate contains extremely high concentrations of zinc, but survives and grows without apparent injury. This begs the question as to how...
Abstract BACKGROUND The prostate contains extremely high concentrations of zinc, but survives and grows without apparent injury. This begs the question as to...
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SubjectTerms apoptosis
cell cycle
HIF-1α
prostate
survivin
zinc
Title Survivin mediates prostate cell protection by HIF-1α against zinc toxicity
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