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ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine

δ-Valerobetaine (δVB) is a constitutive milk metabolite with antioxidant and anti-inflammatory activities. Here, we tested the antineoplastic properties of milk δVB on human colorectal cancer cells. CCD 841 CoN (non-tumorigenic), HT-29 (p53 mutant adenocarcinoma) and LoVo (APC/RAS mutant adenocarcin...

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Autores principales: D’Onofrio, Nunzia, Cacciola, Nunzio Antonio, Martino, Elisa, Borrelli, Francesca, Fiorino, Ferdinando, Lombardi, Assunta, Neglia, Gianluca, Balestrieri, Maria Luisa, Campanile, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265370/
https://www.ncbi.nlm.nih.gov/pubmed/32488123
http://dx.doi.org/10.1038/s41598-020-65865-6
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author D’Onofrio, Nunzia
Cacciola, Nunzio Antonio
Martino, Elisa
Borrelli, Francesca
Fiorino, Ferdinando
Lombardi, Assunta
Neglia, Gianluca
Balestrieri, Maria Luisa
Campanile, Giuseppe
author_facet D’Onofrio, Nunzia
Cacciola, Nunzio Antonio
Martino, Elisa
Borrelli, Francesca
Fiorino, Ferdinando
Lombardi, Assunta
Neglia, Gianluca
Balestrieri, Maria Luisa
Campanile, Giuseppe
author_sort D’Onofrio, Nunzia
collection PubMed
description δ-Valerobetaine (δVB) is a constitutive milk metabolite with antioxidant and anti-inflammatory activities. Here, we tested the antineoplastic properties of milk δVB on human colorectal cancer cells. CCD 841 CoN (non-tumorigenic), HT-29 (p53 mutant adenocarcinoma) and LoVo (APC/RAS mutant adenocarcinoma) cells were exposed to 3 kDa milk extract, δVB (2 mM) or milk+δVB up to 72 h. Results showed a time- and dose-dependent capability of δVB to inhibit cancer cell viability, with higher potency in LoVo cells. Treatment with milk+δVB arrested cell cycle in G2/M and SubG1 phases by upregulating p21, cyclin A, cyclin B1 and p53 protein expressions. Noteworthy, δVB also increased necrosis (P < 0.01) and when used in combination with milk it improved its activity on live cell reduction (P < 0.05) and necrosis (P < 0.05). δVB-enriched milk activated caspase 3, caspase 9, Bax/Bcl-2 apoptotic pathway and reactive oxygen species (ROS) production, whereas no effects on ROS generation were observed in CCD 841 CoN cells. The altered redox homeostasis induced by milk+δVB was accompanied by upregulation of sirtuin 6 (SIRT6). SIRT6 silencing by small interfering RNA blocked autophagy and apoptosis activated by milk+δVB, unveiling the role of this sirtuin in the ROS-mediated apoptotic LoVo cell death.
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spelling pubmed-72653702020-06-05 ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine D’Onofrio, Nunzia Cacciola, Nunzio Antonio Martino, Elisa Borrelli, Francesca Fiorino, Ferdinando Lombardi, Assunta Neglia, Gianluca Balestrieri, Maria Luisa Campanile, Giuseppe Sci Rep Article δ-Valerobetaine (δVB) is a constitutive milk metabolite with antioxidant and anti-inflammatory activities. Here, we tested the antineoplastic properties of milk δVB on human colorectal cancer cells. CCD 841 CoN (non-tumorigenic), HT-29 (p53 mutant adenocarcinoma) and LoVo (APC/RAS mutant adenocarcinoma) cells were exposed to 3 kDa milk extract, δVB (2 mM) or milk+δVB up to 72 h. Results showed a time- and dose-dependent capability of δVB to inhibit cancer cell viability, with higher potency in LoVo cells. Treatment with milk+δVB arrested cell cycle in G2/M and SubG1 phases by upregulating p21, cyclin A, cyclin B1 and p53 protein expressions. Noteworthy, δVB also increased necrosis (P < 0.01) and when used in combination with milk it improved its activity on live cell reduction (P < 0.05) and necrosis (P < 0.05). δVB-enriched milk activated caspase 3, caspase 9, Bax/Bcl-2 apoptotic pathway and reactive oxygen species (ROS) production, whereas no effects on ROS generation were observed in CCD 841 CoN cells. The altered redox homeostasis induced by milk+δVB was accompanied by upregulation of sirtuin 6 (SIRT6). SIRT6 silencing by small interfering RNA blocked autophagy and apoptosis activated by milk+δVB, unveiling the role of this sirtuin in the ROS-mediated apoptotic LoVo cell death. Nature Publishing Group UK 2020-06-02 /pmc/articles/PMC7265370/ /pubmed/32488123 http://dx.doi.org/10.1038/s41598-020-65865-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
D’Onofrio, Nunzia
Cacciola, Nunzio Antonio
Martino, Elisa
Borrelli, Francesca
Fiorino, Ferdinando
Lombardi, Assunta
Neglia, Gianluca
Balestrieri, Maria Luisa
Campanile, Giuseppe
ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine
title ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine
title_full ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine
title_fullStr ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine
title_full_unstemmed ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine
title_short ROS-Mediated Apoptotic Cell Death of Human Colon Cancer LoVo Cells by Milk δ-Valerobetaine
title_sort ros-mediated apoptotic cell death of human colon cancer lovo cells by milk δ-valerobetaine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7265370/
https://www.ncbi.nlm.nih.gov/pubmed/32488123
http://dx.doi.org/10.1038/s41598-020-65865-6
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