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A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress

The present study shows the putative antiproliferative mechanism of action of the previously analytically characterized nudibranch extract (Dolabella auricularia, NB) and its different effects in colon cancer cells vs. nontumor colon cells. NB extract increased the accumulation of reactive oxygen sp...

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Autores principales: Ruiz-Torres, Verónica, Forsythe, Nicholas, Pérez-Sánchez, Almudena, Van Schaeybroeck, Sandra, Barrajón-Catalán, Enrique, Micol, Vicente
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388012/
https://www.ncbi.nlm.nih.gov/pubmed/34456713
http://dx.doi.org/10.3389/fphar.2021.625946
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author Ruiz-Torres, Verónica
Forsythe, Nicholas
Pérez-Sánchez, Almudena
Van Schaeybroeck, Sandra
Barrajón-Catalán, Enrique
Micol, Vicente
author_facet Ruiz-Torres, Verónica
Forsythe, Nicholas
Pérez-Sánchez, Almudena
Van Schaeybroeck, Sandra
Barrajón-Catalán, Enrique
Micol, Vicente
author_sort Ruiz-Torres, Verónica
collection PubMed
description The present study shows the putative antiproliferative mechanism of action of the previously analytically characterized nudibranch extract (Dolabella auricularia, NB) and its different effects in colon cancer cells vs. nontumor colon cells. NB extract increased the accumulation of reactive oxygen species (ROS) and increased endoplasmic reticulum (ER) stress via stimulation of the unfolded protein response. Stress scavengers, N-acetylcysteine (NAC) and 4-phenylbutyric acid (4-PBA), decreased the stress induced by NB. The results showed that NB extract increased ER stress through overproduction of ROS in superinvasive colon cancer cells, decreased their resistance threshold, and produced a nonreturn level of ER stress, causing DNA damage and cell cycle arrest, which prevented them from achieving hyperproliferative capacity and migrating to and invading other tissues. On the contrary, NB extract had a considerably lower effect on nontumor human colon cells, suggesting a selective effect related to stress balance homeostasis. In conclusion, our results confirm that the growth and malignancy of colon cancer cells can be decreased by marine compounds through the modification of one of the most potent resistance mechanisms present in tumor cells; this characteristic differentiates cancer cells from nontumor cells in terms of stress balance.
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spelling pubmed-83880122021-08-27 A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress Ruiz-Torres, Verónica Forsythe, Nicholas Pérez-Sánchez, Almudena Van Schaeybroeck, Sandra Barrajón-Catalán, Enrique Micol, Vicente Front Pharmacol Pharmacology The present study shows the putative antiproliferative mechanism of action of the previously analytically characterized nudibranch extract (Dolabella auricularia, NB) and its different effects in colon cancer cells vs. nontumor colon cells. NB extract increased the accumulation of reactive oxygen species (ROS) and increased endoplasmic reticulum (ER) stress via stimulation of the unfolded protein response. Stress scavengers, N-acetylcysteine (NAC) and 4-phenylbutyric acid (4-PBA), decreased the stress induced by NB. The results showed that NB extract increased ER stress through overproduction of ROS in superinvasive colon cancer cells, decreased their resistance threshold, and produced a nonreturn level of ER stress, causing DNA damage and cell cycle arrest, which prevented them from achieving hyperproliferative capacity and migrating to and invading other tissues. On the contrary, NB extract had a considerably lower effect on nontumor human colon cells, suggesting a selective effect related to stress balance homeostasis. In conclusion, our results confirm that the growth and malignancy of colon cancer cells can be decreased by marine compounds through the modification of one of the most potent resistance mechanisms present in tumor cells; this characteristic differentiates cancer cells from nontumor cells in terms of stress balance. Frontiers Media S.A. 2021-04-08 /pmc/articles/PMC8388012/ /pubmed/34456713 http://dx.doi.org/10.3389/fphar.2021.625946 Text en Copyright © 2021 Ruiz-Torres, Forsythe, Pérez-Sánchez, Van Schaeybroeck, Barrajón-Catalán and Micol. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Ruiz-Torres, Verónica
Forsythe, Nicholas
Pérez-Sánchez, Almudena
Van Schaeybroeck, Sandra
Barrajón-Catalán, Enrique
Micol, Vicente
A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress
title A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress
title_full A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress
title_fullStr A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress
title_full_unstemmed A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress
title_short A Nudibranch Marine Extract Selectively Chemosensitizes Colorectal Cancer Cells by Inducing ROS-Mediated Endoplasmic Reticulum Stress
title_sort nudibranch marine extract selectively chemosensitizes colorectal cancer cells by inducing ros-mediated endoplasmic reticulum stress
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8388012/
https://www.ncbi.nlm.nih.gov/pubmed/34456713
http://dx.doi.org/10.3389/fphar.2021.625946
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