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Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer

Colorectal cancer (CRC), a multifactorial disease, is usually induced and developed through complex mechanisms, including impact of diet and lifestyle, genomic abnormalities, change of signaling pathways, inflammatory response, oxidation stress, dysbiosis, and so on. As natural polyphenolic phytoche...

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Autores principales: Wang, Shi-Tong, Cui, Wen-Qi, Pan, Dan, Jiang, Min, Chang, Bing, Sang, Li-Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029350/
https://www.ncbi.nlm.nih.gov/pubmed/32103869
http://dx.doi.org/10.3748/wjg.v26.i6.562
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author Wang, Shi-Tong
Cui, Wen-Qi
Pan, Dan
Jiang, Min
Chang, Bing
Sang, Li-Xuan
author_facet Wang, Shi-Tong
Cui, Wen-Qi
Pan, Dan
Jiang, Min
Chang, Bing
Sang, Li-Xuan
author_sort Wang, Shi-Tong
collection PubMed
description Colorectal cancer (CRC), a multifactorial disease, is usually induced and developed through complex mechanisms, including impact of diet and lifestyle, genomic abnormalities, change of signaling pathways, inflammatory response, oxidation stress, dysbiosis, and so on. As natural polyphenolic phytochemicals that exist primarily in tea, tea polyphenols (TPs) have been shown to have many clinical applications, especially as anticancer agents. Most animal studies and epidemiological studies have demonstrated that TPs can prevent and treat CRC. TPs can inhibit the growth and metastasis of CRC by exerting the anti-inflammatory, anti-oxidative or pro-oxidative, and pro-apoptotic effects, which are achieved by modulations at multiple levels. Many experiments have demonstrated that TPs can modulate several signaling pathways in cancer cells, including the mitogen-activated protein kinase pathway, phosphatidylinositol-3 kinase/Akt pathway, Wnt/β-catenin pathway, and 67 kDa laminin receptor pathway, to inhibit proliferation and promote cell apoptosis. In addition, novel studies have also suggested that TPs can prevent the growth and metastasis of CRC by modulating the composition of gut microbiota to improve immune system and decrease inflammatory responses. Molecular pathological epidemiology, a novel multidisciplinary investigation, has made great progress on CRC, and the further molecular pathological epidemiology research should be developed in the field of TPs and CRC. This review summarizes the existing in vitro and in vivo animal and human studies and potential mechanisms to examine the effects of tea polyphenols on CRC.
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spelling pubmed-70293502020-02-26 Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer Wang, Shi-Tong Cui, Wen-Qi Pan, Dan Jiang, Min Chang, Bing Sang, Li-Xuan World J Gastroenterol Review Colorectal cancer (CRC), a multifactorial disease, is usually induced and developed through complex mechanisms, including impact of diet and lifestyle, genomic abnormalities, change of signaling pathways, inflammatory response, oxidation stress, dysbiosis, and so on. As natural polyphenolic phytochemicals that exist primarily in tea, tea polyphenols (TPs) have been shown to have many clinical applications, especially as anticancer agents. Most animal studies and epidemiological studies have demonstrated that TPs can prevent and treat CRC. TPs can inhibit the growth and metastasis of CRC by exerting the anti-inflammatory, anti-oxidative or pro-oxidative, and pro-apoptotic effects, which are achieved by modulations at multiple levels. Many experiments have demonstrated that TPs can modulate several signaling pathways in cancer cells, including the mitogen-activated protein kinase pathway, phosphatidylinositol-3 kinase/Akt pathway, Wnt/β-catenin pathway, and 67 kDa laminin receptor pathway, to inhibit proliferation and promote cell apoptosis. In addition, novel studies have also suggested that TPs can prevent the growth and metastasis of CRC by modulating the composition of gut microbiota to improve immune system and decrease inflammatory responses. Molecular pathological epidemiology, a novel multidisciplinary investigation, has made great progress on CRC, and the further molecular pathological epidemiology research should be developed in the field of TPs and CRC. This review summarizes the existing in vitro and in vivo animal and human studies and potential mechanisms to examine the effects of tea polyphenols on CRC. Baishideng Publishing Group Inc 2020-02-14 2020-02-14 /pmc/articles/PMC7029350/ /pubmed/32103869 http://dx.doi.org/10.3748/wjg.v26.i6.562 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Review
Wang, Shi-Tong
Cui, Wen-Qi
Pan, Dan
Jiang, Min
Chang, Bing
Sang, Li-Xuan
Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer
title Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer
title_full Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer
title_fullStr Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer
title_full_unstemmed Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer
title_short Tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer
title_sort tea polyphenols and their chemopreventive and therapeutic effects on colorectal cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029350/
https://www.ncbi.nlm.nih.gov/pubmed/32103869
http://dx.doi.org/10.3748/wjg.v26.i6.562
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