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The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells

Ethanolic extracts from Mangifera indica L. have been proved to possess anti-tumor properties in many cancer systems. However, although most effects have been demonstrated with fruit pulp extract, the underlying molecular mechanisms of mango peel are still unclear. This study was designed to explore...

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Autores principales: Lauricella, Marianna, Lo Galbo, Valentina, Cernigliaro, Cesare, Maggio, Antonella, Palumbo Piccionello, Antonio, Calvaruso, Giuseppe, Carlisi, Daniela, Emanuele, Sonia, Giuliano, Michela, D’Anneo, Antonella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826946/
https://www.ncbi.nlm.nih.gov/pubmed/31546694
http://dx.doi.org/10.3390/antiox8100422
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author Lauricella, Marianna
Lo Galbo, Valentina
Cernigliaro, Cesare
Maggio, Antonella
Palumbo Piccionello, Antonio
Calvaruso, Giuseppe
Carlisi, Daniela
Emanuele, Sonia
Giuliano, Michela
D’Anneo, Antonella
author_facet Lauricella, Marianna
Lo Galbo, Valentina
Cernigliaro, Cesare
Maggio, Antonella
Palumbo Piccionello, Antonio
Calvaruso, Giuseppe
Carlisi, Daniela
Emanuele, Sonia
Giuliano, Michela
D’Anneo, Antonella
author_sort Lauricella, Marianna
collection PubMed
description Ethanolic extracts from Mangifera indica L. have been proved to possess anti-tumor properties in many cancer systems. However, although most effects have been demonstrated with fruit pulp extract, the underlying molecular mechanisms of mango peel are still unclear. This study was designed to explore the effects of mango peel extract (MPE) on colon cancer cell lines. MPE affected cell viability and inhibited the colony formation trend of tumor cells, while no effects were observed in human dermal fibroblasts used as a non-cancerous cell line model. These events were a consequence of the induction of apoptosis associated to reactive oxygen species (ROS) production, activation of players of the oxidative response such as JNK and ERK1/2, and the increase in Nrf2 and manganese superoxide dismutase (MnSOD). Significantly, mango peel-activated stress triggered a DNA damage response evidenced by the precocious phosphorylation of histone 2AX (γH2AX), as well as phosphorylated Ataxia telangiectasia-mutated (ATM) kinase and p53 upregulation. Mango peel extract was also characterized, and HPLC/MS (High Performance Liquid Chromatography/Mass Spectrometry) analysis unveiled the presence of some phenolic compounds that could be responsible for the anti-cancer effects. Collectively, these findings point out the importance of the genotoxic stress signaling pathway mediated by γH2AX in targeting colon tumor cells to apoptosis.
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spelling pubmed-68269462019-11-18 The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells Lauricella, Marianna Lo Galbo, Valentina Cernigliaro, Cesare Maggio, Antonella Palumbo Piccionello, Antonio Calvaruso, Giuseppe Carlisi, Daniela Emanuele, Sonia Giuliano, Michela D’Anneo, Antonella Antioxidants (Basel) Article Ethanolic extracts from Mangifera indica L. have been proved to possess anti-tumor properties in many cancer systems. However, although most effects have been demonstrated with fruit pulp extract, the underlying molecular mechanisms of mango peel are still unclear. This study was designed to explore the effects of mango peel extract (MPE) on colon cancer cell lines. MPE affected cell viability and inhibited the colony formation trend of tumor cells, while no effects were observed in human dermal fibroblasts used as a non-cancerous cell line model. These events were a consequence of the induction of apoptosis associated to reactive oxygen species (ROS) production, activation of players of the oxidative response such as JNK and ERK1/2, and the increase in Nrf2 and manganese superoxide dismutase (MnSOD). Significantly, mango peel-activated stress triggered a DNA damage response evidenced by the precocious phosphorylation of histone 2AX (γH2AX), as well as phosphorylated Ataxia telangiectasia-mutated (ATM) kinase and p53 upregulation. Mango peel extract was also characterized, and HPLC/MS (High Performance Liquid Chromatography/Mass Spectrometry) analysis unveiled the presence of some phenolic compounds that could be responsible for the anti-cancer effects. Collectively, these findings point out the importance of the genotoxic stress signaling pathway mediated by γH2AX in targeting colon tumor cells to apoptosis. MDPI 2019-09-22 /pmc/articles/PMC6826946/ /pubmed/31546694 http://dx.doi.org/10.3390/antiox8100422 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lauricella, Marianna
Lo Galbo, Valentina
Cernigliaro, Cesare
Maggio, Antonella
Palumbo Piccionello, Antonio
Calvaruso, Giuseppe
Carlisi, Daniela
Emanuele, Sonia
Giuliano, Michela
D’Anneo, Antonella
The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells
title The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells
title_full The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells
title_fullStr The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells
title_full_unstemmed The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells
title_short The Anti-Cancer Effect of Mangifera indica L. Peel Extract is Associated to γH2AX-mediated Apoptosis in Colon Cancer Cells
title_sort anti-cancer effect of mangifera indica l. peel extract is associated to γh2ax-mediated apoptosis in colon cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826946/
https://www.ncbi.nlm.nih.gov/pubmed/31546694
http://dx.doi.org/10.3390/antiox8100422
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