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Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro

Electrochemical reduced water (ERW) has been proposed to have beneficial effects on human health due to its rich content of H(2) and the presence of platinum nanoparticles with antioxidant effects. Many studies have demonstrated that ERW scavenging properties are able to reduce the damage caused by...

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Autores principales: Frajese, Giovanni Vanni, Benvenuto, Monica, Mattera, Rosanna, Giampaoli, Saverio, Ambrosin, Elena, Bernardini, Roberta, Giganti, Maria Gabriella, Albonici, Loredana, Dus, Ivan, Manzari, Vittorio, Modesti, Andrea, Mattei, Maurizio, Bei, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196883/
https://www.ncbi.nlm.nih.gov/pubmed/30402124
http://dx.doi.org/10.1155/2018/4753507
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author Frajese, Giovanni Vanni
Benvenuto, Monica
Mattera, Rosanna
Giampaoli, Saverio
Ambrosin, Elena
Bernardini, Roberta
Giganti, Maria Gabriella
Albonici, Loredana
Dus, Ivan
Manzari, Vittorio
Modesti, Andrea
Mattei, Maurizio
Bei, Roberto
author_facet Frajese, Giovanni Vanni
Benvenuto, Monica
Mattera, Rosanna
Giampaoli, Saverio
Ambrosin, Elena
Bernardini, Roberta
Giganti, Maria Gabriella
Albonici, Loredana
Dus, Ivan
Manzari, Vittorio
Modesti, Andrea
Mattei, Maurizio
Bei, Roberto
author_sort Frajese, Giovanni Vanni
collection PubMed
description Electrochemical reduced water (ERW) has been proposed to have beneficial effects on human health due to its rich content of H(2) and the presence of platinum nanoparticles with antioxidant effects. Many studies have demonstrated that ERW scavenging properties are able to reduce the damage caused by oxidative stress in different experimental models. Although few in vivo studies have been reported, it has been demonstrated that ERW may display anticancer effects by induction of tumor cells apoptosis and reduction of both angiogenesis and inflammation. In this study, we show that ERW treatment of MCF-7, MDA-MB-453, and mouse (TUBO) breast cancer cells inhibited cell survival in a time-dependent fashion. ERW decreased ErbB2/neu expression and impaired pERK1/ERK2 and AKT phosphorylation in breast cancer cells. In addition, ERW treatment induced apoptosis of breast cancer cell lines independently of the status of p53 and ER and PR receptors. Our in vivo results showed that ERW treatment of transgenic BALB-neuT mice delayed the development of mammary tumors compared to the control. In addition, ERW induced a significant prolongation of tumor-free survival and a reduction in tumor multiplicity. Overall, these results suggest a potential beneficial role of ERW in inhibiting cancer cells growth.
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spelling pubmed-61968832018-11-06 Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro Frajese, Giovanni Vanni Benvenuto, Monica Mattera, Rosanna Giampaoli, Saverio Ambrosin, Elena Bernardini, Roberta Giganti, Maria Gabriella Albonici, Loredana Dus, Ivan Manzari, Vittorio Modesti, Andrea Mattei, Maurizio Bei, Roberto Evid Based Complement Alternat Med Research Article Electrochemical reduced water (ERW) has been proposed to have beneficial effects on human health due to its rich content of H(2) and the presence of platinum nanoparticles with antioxidant effects. Many studies have demonstrated that ERW scavenging properties are able to reduce the damage caused by oxidative stress in different experimental models. Although few in vivo studies have been reported, it has been demonstrated that ERW may display anticancer effects by induction of tumor cells apoptosis and reduction of both angiogenesis and inflammation. In this study, we show that ERW treatment of MCF-7, MDA-MB-453, and mouse (TUBO) breast cancer cells inhibited cell survival in a time-dependent fashion. ERW decreased ErbB2/neu expression and impaired pERK1/ERK2 and AKT phosphorylation in breast cancer cells. In addition, ERW treatment induced apoptosis of breast cancer cell lines independently of the status of p53 and ER and PR receptors. Our in vivo results showed that ERW treatment of transgenic BALB-neuT mice delayed the development of mammary tumors compared to the control. In addition, ERW induced a significant prolongation of tumor-free survival and a reduction in tumor multiplicity. Overall, these results suggest a potential beneficial role of ERW in inhibiting cancer cells growth. Hindawi 2018-09-26 /pmc/articles/PMC6196883/ /pubmed/30402124 http://dx.doi.org/10.1155/2018/4753507 Text en Copyright © 2018 Giovanni Vanni Frajese et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Frajese, Giovanni Vanni
Benvenuto, Monica
Mattera, Rosanna
Giampaoli, Saverio
Ambrosin, Elena
Bernardini, Roberta
Giganti, Maria Gabriella
Albonici, Loredana
Dus, Ivan
Manzari, Vittorio
Modesti, Andrea
Mattei, Maurizio
Bei, Roberto
Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro
title Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro
title_full Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro
title_fullStr Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro
title_full_unstemmed Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro
title_short Electrochemically Reduced Water Delays Mammary Tumors Growth in Mice and Inhibits Breast Cancer Cells Survival In Vitro
title_sort electrochemically reduced water delays mammary tumors growth in mice and inhibits breast cancer cells survival in vitro
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196883/
https://www.ncbi.nlm.nih.gov/pubmed/30402124
http://dx.doi.org/10.1155/2018/4753507
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