Zinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.

<h4>Background</h4>Hypoxia inducible factor-1α (HIF-1α) is responsible for the majority of HIF-1-induced gene expression changes under hypoxia and for the "angiogenic switch" during tumor progression. HIF-1α is often upregulated in tumors leading to more aggressive tumor growth...

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Autores principales: Lavinia Nardinocchi, Valentina Pantisano, Rosa Puca, Manuela Porru, Aurora Aiello, Annalisa Grasselli, Carlo Leonetti, Michal Safran, Gideon Rechavi, David Givol, Antonella Farsetti, Gabriella D'Orazi
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Publicado: Public Library of Science (PLoS) 2010
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spelling oai:doaj.org-article:ab2a4d89211047d4bc42ddf4cf41d1bc2021-11-18T07:01:49ZZinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.1932-620310.1371/journal.pone.0015048https://doaj.org/article/ab2a4d89211047d4bc42ddf4cf41d1bc2010-12-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21179202/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Hypoxia inducible factor-1α (HIF-1α) is responsible for the majority of HIF-1-induced gene expression changes under hypoxia and for the "angiogenic switch" during tumor progression. HIF-1α is often upregulated in tumors leading to more aggressive tumor growth and chemoresistance, therefore representing an important target for antitumor intervention. We previously reported that zinc downregulated HIF-1α levels. Here, we evaluated the molecular mechanisms of zinc-induced HIF-1α downregulation and whether zinc affected HIF-1α also in vivo.<h4>Methodology/principal findings</h4>Here we report that zinc downregulated HIF-1α protein levels in human prostate cancer and glioblastoma cells under hypoxia, whether induced or constitutive. Investigations into the molecular mechanisms showed that zinc induced HIF-1α proteasomal degradation that was prevented by treatment with proteasomal inhibitor MG132. HIF-1α downregulation induced by zinc was ineffective in human RCC4 VHL-null renal carcinoma cell line; likewise, the HIF-1αP402/P564A mutant was resistant to zinc treatment. Similarly to HIF-1α, zinc downregulated also hypoxia-induced HIF-2α whereas the HIF-1β subunit remained unchanged. Zinc inhibited HIF-1α recruitment onto VEGF promoter and the zinc-induced suppression of HIF-1-dependent activation of VEGF correlated with reduction of glioblastoma and prostate cancer cell invasiveness in vitro. Finally, zinc administration downregulated HIF-1α levels in vivo, by bioluminescence imaging, and suppressed intratumoral VEGF expression.<h4>Conclusions/significance</h4>These findings, by demonstrating that zinc induces HIF-1α proteasomal degradation, indicate that zinc could be useful as an inhibitor of HIF-1α in human tumors to repress important pathways involved in tumor progression, such as those induced by VEGF, MDR1, and Bcl2 target genes, and hopefully potentiate the anticancer therapies.Lavinia NardinocchiValentina PantisanoRosa PucaManuela PorruAurora AielloAnnalisa GrasselliCarlo LeonettiMichal SafranGideon RechaviDavid GivolAntonella FarsettiGabriella D'OraziPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 12, p e15048 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Lavinia Nardinocchi
Valentina Pantisano
Rosa Puca
Manuela Porru
Aurora Aiello
Annalisa Grasselli
Carlo Leonetti
Michal Safran
Gideon Rechavi
David Givol
Antonella Farsetti
Gabriella D'Orazi
Zinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.
description <h4>Background</h4>Hypoxia inducible factor-1α (HIF-1α) is responsible for the majority of HIF-1-induced gene expression changes under hypoxia and for the "angiogenic switch" during tumor progression. HIF-1α is often upregulated in tumors leading to more aggressive tumor growth and chemoresistance, therefore representing an important target for antitumor intervention. We previously reported that zinc downregulated HIF-1α levels. Here, we evaluated the molecular mechanisms of zinc-induced HIF-1α downregulation and whether zinc affected HIF-1α also in vivo.<h4>Methodology/principal findings</h4>Here we report that zinc downregulated HIF-1α protein levels in human prostate cancer and glioblastoma cells under hypoxia, whether induced or constitutive. Investigations into the molecular mechanisms showed that zinc induced HIF-1α proteasomal degradation that was prevented by treatment with proteasomal inhibitor MG132. HIF-1α downregulation induced by zinc was ineffective in human RCC4 VHL-null renal carcinoma cell line; likewise, the HIF-1αP402/P564A mutant was resistant to zinc treatment. Similarly to HIF-1α, zinc downregulated also hypoxia-induced HIF-2α whereas the HIF-1β subunit remained unchanged. Zinc inhibited HIF-1α recruitment onto VEGF promoter and the zinc-induced suppression of HIF-1-dependent activation of VEGF correlated with reduction of glioblastoma and prostate cancer cell invasiveness in vitro. Finally, zinc administration downregulated HIF-1α levels in vivo, by bioluminescence imaging, and suppressed intratumoral VEGF expression.<h4>Conclusions/significance</h4>These findings, by demonstrating that zinc induces HIF-1α proteasomal degradation, indicate that zinc could be useful as an inhibitor of HIF-1α in human tumors to repress important pathways involved in tumor progression, such as those induced by VEGF, MDR1, and Bcl2 target genes, and hopefully potentiate the anticancer therapies.
format article
author Lavinia Nardinocchi
Valentina Pantisano
Rosa Puca
Manuela Porru
Aurora Aiello
Annalisa Grasselli
Carlo Leonetti
Michal Safran
Gideon Rechavi
David Givol
Antonella Farsetti
Gabriella D'Orazi
author_facet Lavinia Nardinocchi
Valentina Pantisano
Rosa Puca
Manuela Porru
Aurora Aiello
Annalisa Grasselli
Carlo Leonetti
Michal Safran
Gideon Rechavi
David Givol
Antonella Farsetti
Gabriella D'Orazi
author_sort Lavinia Nardinocchi
title Zinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.
title_short Zinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.
title_full Zinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.
title_fullStr Zinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.
title_full_unstemmed Zinc downregulates HIF-1α and inhibits its activity in tumor cells in vitro and in vivo.
title_sort zinc downregulates hif-1α and inhibits its activity in tumor cells in vitro and in vivo.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/ab2a4d89211047d4bc42ddf4cf41d1bc
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