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Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment
Colorectal cancer is the third most common form of cancer diagnosed and the third leading class for cancer-related deaths. Given the prevalence of colon cancer worldwide, further insight into developing novel and effective prevention and treatment strategies are warranted. The family of plant pigmen...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664094/ https://www.ncbi.nlm.nih.gov/pubmed/34926717 http://dx.doi.org/10.18632/oncoscience.548 |
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author | Mudd, Ashley M. Gu, Tao Munagala, Radha Jeyabalan, Jeyaprakash Fraig, Mostafa Egilmez, Nejat K. Gupta, Ramesh C. |
author_facet | Mudd, Ashley M. Gu, Tao Munagala, Radha Jeyabalan, Jeyaprakash Fraig, Mostafa Egilmez, Nejat K. Gupta, Ramesh C. |
author_sort | Mudd, Ashley M. |
collection | PubMed |
description | Colorectal cancer is the third most common form of cancer diagnosed and the third leading class for cancer-related deaths. Given the prevalence of colon cancer worldwide, further insight into developing novel and effective prevention and treatment strategies are warranted. The family of plant pigments known as the anthocyanins has been identified with a variety of health benefits including chemopreventive and therapeutic effects. A limitation to current clinical applications of anthocyanins is the high doses that are required. In order to overcome this limitation, we tested the active moiety, anthocyanidins for chemopreventive and therapeutic effects against colorectal cancer in vivo and in vitro. Treatment with native anthocyanidin mixture (Anthos) from bilberry yielded significant antiproliferative activity against colon cancer cells. Anthos treatment led to significant reductions in polyp and tumor counts in vivo. Reduced Src and EGFR phosphorylation was observed with Anthos treatment, which correlated with downstream targets such as PD-L1 and modulation of the colon inflammatory environment. These results provide a promising outlook on the impact of berry Anthos for the treatment and prevention of familial adenomatous polyposis and colorectal cancer. Results from this study also provide novel mechanistic insight into the chemopreventive and therapeutic activities of Anthos. |
format | Online Article Text |
id | pubmed-8664094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-86640942021-12-16 Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment Mudd, Ashley M. Gu, Tao Munagala, Radha Jeyabalan, Jeyaprakash Fraig, Mostafa Egilmez, Nejat K. Gupta, Ramesh C. Oncoscience Research Paper Colorectal cancer is the third most common form of cancer diagnosed and the third leading class for cancer-related deaths. Given the prevalence of colon cancer worldwide, further insight into developing novel and effective prevention and treatment strategies are warranted. The family of plant pigments known as the anthocyanins has been identified with a variety of health benefits including chemopreventive and therapeutic effects. A limitation to current clinical applications of anthocyanins is the high doses that are required. In order to overcome this limitation, we tested the active moiety, anthocyanidins for chemopreventive and therapeutic effects against colorectal cancer in vivo and in vitro. Treatment with native anthocyanidin mixture (Anthos) from bilberry yielded significant antiproliferative activity against colon cancer cells. Anthos treatment led to significant reductions in polyp and tumor counts in vivo. Reduced Src and EGFR phosphorylation was observed with Anthos treatment, which correlated with downstream targets such as PD-L1 and modulation of the colon inflammatory environment. These results provide a promising outlook on the impact of berry Anthos for the treatment and prevention of familial adenomatous polyposis and colorectal cancer. Results from this study also provide novel mechanistic insight into the chemopreventive and therapeutic activities of Anthos. Impact Journals LLC 2021-12-10 /pmc/articles/PMC8664094/ /pubmed/34926717 http://dx.doi.org/10.18632/oncoscience.548 Text en https://creativecommons.org/licenses/by/3.0/Copyright: © 2021 Mudd et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Mudd, Ashley M. Gu, Tao Munagala, Radha Jeyabalan, Jeyaprakash Fraig, Mostafa Egilmez, Nejat K. Gupta, Ramesh C. Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment |
title | Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment |
title_full | Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment |
title_fullStr | Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment |
title_full_unstemmed | Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment |
title_short | Berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of Src, EGFR and the colon inflammatory environment |
title_sort | berry anthocyanidins inhibit intestinal polyps and colon tumors by modulation of src, egfr and the colon inflammatory environment |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664094/ https://www.ncbi.nlm.nih.gov/pubmed/34926717 http://dx.doi.org/10.18632/oncoscience.548 |
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