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ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells

Lipid Droplets (LDs) are emerging as crucial players in colon cancer development and maintenance. Their expression has been associated with high tumorigenicity in Cancer Stem Cells (CSCs), so that they have been proposed as a new functional marker in Colorectal Cancer Stem Cells (CR-CSCs). They are...

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Autores principales: Tirinato, Luca, Pagliari, Francesca, Di Franco, Simone, Sogne, Elisa, Marafioti, Maria Grazia, Jansen, Jeanette, Falqui, Andrea, Todaro, Matilde, Candeloro, Patrizio, Liberale, Carlo, Seco, Joao, Stassi, Giorgio, Di Fabrizio, Enzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729111/
https://www.ncbi.nlm.nih.gov/pubmed/33335962
http://dx.doi.org/10.1016/j.gendis.2019.09.010
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author Tirinato, Luca
Pagliari, Francesca
Di Franco, Simone
Sogne, Elisa
Marafioti, Maria Grazia
Jansen, Jeanette
Falqui, Andrea
Todaro, Matilde
Candeloro, Patrizio
Liberale, Carlo
Seco, Joao
Stassi, Giorgio
Di Fabrizio, Enzo
author_facet Tirinato, Luca
Pagliari, Francesca
Di Franco, Simone
Sogne, Elisa
Marafioti, Maria Grazia
Jansen, Jeanette
Falqui, Andrea
Todaro, Matilde
Candeloro, Patrizio
Liberale, Carlo
Seco, Joao
Stassi, Giorgio
Di Fabrizio, Enzo
author_sort Tirinato, Luca
collection PubMed
description Lipid Droplets (LDs) are emerging as crucial players in colon cancer development and maintenance. Their expression has been associated with high tumorigenicity in Cancer Stem Cells (CSCs), so that they have been proposed as a new functional marker in Colorectal Cancer Stem Cells (CR-CSCs). They are also indirectly involved in the modulation of the tumor microenvironment through the production of pro-inflammatory molecules. There is growing evidence that a possible connection between metabolic alterations and malignant transformation exists, although the effects of nutrients, primarily glucose, on the CSC behavior are still mostly unexplored. Glucose is an essential fuel for cancer cells, and the connections with LDs in the healthy and CSC populations merit to be more deeply investigated. Here, we showed that a high glucose concentration activated the PI3K/AKT pathway and increased the expression of CD133 and CD44v6 CSC markers. Additionally, glucose was responsible for the increased amount of Reactive Oxygen Species (ROS) and LDs in both healthy and CR-CSC samples. We also investigated the gene modulations following the HG treatment and found out that the healthy cell gene profile was the most affected. Lastly, Atorvastatin, a lipid-lowering drug, induced the highest mortality on CR-CSCs without affecting the healthy counterpart.
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spelling pubmed-77291112020-12-16 ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells Tirinato, Luca Pagliari, Francesca Di Franco, Simone Sogne, Elisa Marafioti, Maria Grazia Jansen, Jeanette Falqui, Andrea Todaro, Matilde Candeloro, Patrizio Liberale, Carlo Seco, Joao Stassi, Giorgio Di Fabrizio, Enzo Genes Dis Full Length Article Lipid Droplets (LDs) are emerging as crucial players in colon cancer development and maintenance. Their expression has been associated with high tumorigenicity in Cancer Stem Cells (CSCs), so that they have been proposed as a new functional marker in Colorectal Cancer Stem Cells (CR-CSCs). They are also indirectly involved in the modulation of the tumor microenvironment through the production of pro-inflammatory molecules. There is growing evidence that a possible connection between metabolic alterations and malignant transformation exists, although the effects of nutrients, primarily glucose, on the CSC behavior are still mostly unexplored. Glucose is an essential fuel for cancer cells, and the connections with LDs in the healthy and CSC populations merit to be more deeply investigated. Here, we showed that a high glucose concentration activated the PI3K/AKT pathway and increased the expression of CD133 and CD44v6 CSC markers. Additionally, glucose was responsible for the increased amount of Reactive Oxygen Species (ROS) and LDs in both healthy and CR-CSC samples. We also investigated the gene modulations following the HG treatment and found out that the healthy cell gene profile was the most affected. Lastly, Atorvastatin, a lipid-lowering drug, induced the highest mortality on CR-CSCs without affecting the healthy counterpart. Chongqing Medical University 2019-09-25 /pmc/articles/PMC7729111/ /pubmed/33335962 http://dx.doi.org/10.1016/j.gendis.2019.09.010 Text en © 2019 Chongqing Medical University. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Tirinato, Luca
Pagliari, Francesca
Di Franco, Simone
Sogne, Elisa
Marafioti, Maria Grazia
Jansen, Jeanette
Falqui, Andrea
Todaro, Matilde
Candeloro, Patrizio
Liberale, Carlo
Seco, Joao
Stassi, Giorgio
Di Fabrizio, Enzo
ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells
title ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells
title_full ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells
title_fullStr ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells
title_full_unstemmed ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells
title_short ROS and Lipid Droplet accumulation induced by high glucose exposure in healthy colon and Colorectal Cancer Stem Cells
title_sort ros and lipid droplet accumulation induced by high glucose exposure in healthy colon and colorectal cancer stem cells
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729111/
https://www.ncbi.nlm.nih.gov/pubmed/33335962
http://dx.doi.org/10.1016/j.gendis.2019.09.010
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