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The Anti-Cancer Mechanisms of Berberine: A Review
Berberine (BBR) has been extensively studied in vivo and vitro experiments. BBR inhibits cell proliferation by regulating cell cycle and cell autophagy, and promoting cell apoptosis. BBR also inhibits cell invasion and metastasis by suppressing EMT and down-regulating the expression of metastasis-re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996556/ https://www.ncbi.nlm.nih.gov/pubmed/32099466 http://dx.doi.org/10.2147/CMAR.S242329 |
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author | Wang, Ye Liu, Yanfang Du, Xinyang Ma, Hong Yao, Jing |
author_facet | Wang, Ye Liu, Yanfang Du, Xinyang Ma, Hong Yao, Jing |
author_sort | Wang, Ye |
collection | PubMed |
description | Berberine (BBR) has been extensively studied in vivo and vitro experiments. BBR inhibits cell proliferation by regulating cell cycle and cell autophagy, and promoting cell apoptosis. BBR also inhibits cell invasion and metastasis by suppressing EMT and down-regulating the expression of metastasis-related proteins and signaling pathways. In addition, BBR inhibits cell proliferation by interacting with microRNAs and suppressing telomerase activity. BBR exerts its anti-inflammation and antioxidant properties, and also regulates tumor microenvironment. This review emphasized that BBR as a potential anti-inflammation and antioxidant agent, also as an effective immunomodulator, is expected to be widely used in clinic for cancer therapy. |
format | Online Article Text |
id | pubmed-6996556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-69965562020-02-25 The Anti-Cancer Mechanisms of Berberine: A Review Wang, Ye Liu, Yanfang Du, Xinyang Ma, Hong Yao, Jing Cancer Manag Res Review Berberine (BBR) has been extensively studied in vivo and vitro experiments. BBR inhibits cell proliferation by regulating cell cycle and cell autophagy, and promoting cell apoptosis. BBR also inhibits cell invasion and metastasis by suppressing EMT and down-regulating the expression of metastasis-related proteins and signaling pathways. In addition, BBR inhibits cell proliferation by interacting with microRNAs and suppressing telomerase activity. BBR exerts its anti-inflammation and antioxidant properties, and also regulates tumor microenvironment. This review emphasized that BBR as a potential anti-inflammation and antioxidant agent, also as an effective immunomodulator, is expected to be widely used in clinic for cancer therapy. Dove 2020-01-30 /pmc/articles/PMC6996556/ /pubmed/32099466 http://dx.doi.org/10.2147/CMAR.S242329 Text en © 2020 Wang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Review Wang, Ye Liu, Yanfang Du, Xinyang Ma, Hong Yao, Jing The Anti-Cancer Mechanisms of Berberine: A Review |
title | The Anti-Cancer Mechanisms of Berberine: A Review |
title_full | The Anti-Cancer Mechanisms of Berberine: A Review |
title_fullStr | The Anti-Cancer Mechanisms of Berberine: A Review |
title_full_unstemmed | The Anti-Cancer Mechanisms of Berberine: A Review |
title_short | The Anti-Cancer Mechanisms of Berberine: A Review |
title_sort | anti-cancer mechanisms of berberine: a review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996556/ https://www.ncbi.nlm.nih.gov/pubmed/32099466 http://dx.doi.org/10.2147/CMAR.S242329 |
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