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The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells

Carotenoids may have different effects on cancer and its progression. The safety of carotenoid supplements was evaluated in vitro on human non-small cell lung cancer (NSCLC) adenocarcinoma A549 cells by the administration of three different oleoresins containing lycopene and other lipophilic phytoch...

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Autores principales: Di Sano, Caterina, Lazzara, Valentina, Durante, Miriana, D’Anna, Claudia, Bonura, Angela, Dino, Paola, Uasuf, Carina Gabriela, Pace, Elisabetta, Lenucci, Marcello Salvatore, Bruno, Andreina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219748/
https://www.ncbi.nlm.nih.gov/pubmed/35740047
http://dx.doi.org/10.3390/antiox11061150
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author Di Sano, Caterina
Lazzara, Valentina
Durante, Miriana
D’Anna, Claudia
Bonura, Angela
Dino, Paola
Uasuf, Carina Gabriela
Pace, Elisabetta
Lenucci, Marcello Salvatore
Bruno, Andreina
author_facet Di Sano, Caterina
Lazzara, Valentina
Durante, Miriana
D’Anna, Claudia
Bonura, Angela
Dino, Paola
Uasuf, Carina Gabriela
Pace, Elisabetta
Lenucci, Marcello Salvatore
Bruno, Andreina
author_sort Di Sano, Caterina
collection PubMed
description Carotenoids may have different effects on cancer and its progression. The safety of carotenoid supplements was evaluated in vitro on human non-small cell lung cancer (NSCLC) adenocarcinoma A549 cells by the administration of three different oleoresins containing lycopene and other lipophilic phytochemicals, such as tocochromanols. The oleoresins, obtained by the supercritical CO(2) green extraction technology from watermelon (Lyc W), gấc(Lyc G) and tomato (Lyc T) and chlatrated in α-cyclodextrins, were tested in comparison to synthetic lycopene (Lyc S), by cell cycle, Annexin V-FITC/PI, clonogenic test, Mytosox, intracellular ROS, Western Blot for NF-kB and RT-PCR and ELISA for IL-8. The extracts administered at the same lycopene concentration (10 µM) showed conflicting behaviors: Lyc W, with the highest lycopene/tocochromanols ratio, significantly increased cell apoptosis, mitochondrial stress, intracellular ROS, NF-kB and IL-8 expression and significantly decreased cell proliferation, whereas Lyc G and Lyc T significantly increased only cell proliferation. Lyc S treatment was ineffective. The highest amount of lycopene in Lyc W was able to counteract and revert the cell survival effect of tocochromanols supporting the importance of evaluating the lycopene bio-availability and the real effect of antioxidant tocochromanols’ supplementation which may not only have no anticancer benefits but may even increase cancer aggressivity.
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spelling pubmed-92197482022-06-24 The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells Di Sano, Caterina Lazzara, Valentina Durante, Miriana D’Anna, Claudia Bonura, Angela Dino, Paola Uasuf, Carina Gabriela Pace, Elisabetta Lenucci, Marcello Salvatore Bruno, Andreina Antioxidants (Basel) Article Carotenoids may have different effects on cancer and its progression. The safety of carotenoid supplements was evaluated in vitro on human non-small cell lung cancer (NSCLC) adenocarcinoma A549 cells by the administration of three different oleoresins containing lycopene and other lipophilic phytochemicals, such as tocochromanols. The oleoresins, obtained by the supercritical CO(2) green extraction technology from watermelon (Lyc W), gấc(Lyc G) and tomato (Lyc T) and chlatrated in α-cyclodextrins, were tested in comparison to synthetic lycopene (Lyc S), by cell cycle, Annexin V-FITC/PI, clonogenic test, Mytosox, intracellular ROS, Western Blot for NF-kB and RT-PCR and ELISA for IL-8. The extracts administered at the same lycopene concentration (10 µM) showed conflicting behaviors: Lyc W, with the highest lycopene/tocochromanols ratio, significantly increased cell apoptosis, mitochondrial stress, intracellular ROS, NF-kB and IL-8 expression and significantly decreased cell proliferation, whereas Lyc G and Lyc T significantly increased only cell proliferation. Lyc S treatment was ineffective. The highest amount of lycopene in Lyc W was able to counteract and revert the cell survival effect of tocochromanols supporting the importance of evaluating the lycopene bio-availability and the real effect of antioxidant tocochromanols’ supplementation which may not only have no anticancer benefits but may even increase cancer aggressivity. MDPI 2022-06-11 /pmc/articles/PMC9219748/ /pubmed/35740047 http://dx.doi.org/10.3390/antiox11061150 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Di Sano, Caterina
Lazzara, Valentina
Durante, Miriana
D’Anna, Claudia
Bonura, Angela
Dino, Paola
Uasuf, Carina Gabriela
Pace, Elisabetta
Lenucci, Marcello Salvatore
Bruno, Andreina
The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells
title The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells
title_full The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells
title_fullStr The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells
title_full_unstemmed The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells
title_short The Protective Anticancer Effect of Natural Lycopene Supercritical CO(2) Watermelon Extracts in Adenocarcinoma Lung Cancer Cells
title_sort protective anticancer effect of natural lycopene supercritical co(2) watermelon extracts in adenocarcinoma lung cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9219748/
https://www.ncbi.nlm.nih.gov/pubmed/35740047
http://dx.doi.org/10.3390/antiox11061150
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