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Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark
BACKGROUND: Root bark of mulberry (Morus alba L.) has been used in herbal medicine as anti-phlogistic, liver protective, kidney protective, hypotensive, diuretic, anti-cough and analgesic agent. However, the anti-cancer activity and the potential anti-cancer mechanisms of mulberry root bark have not...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074313/ https://www.ncbi.nlm.nih.gov/pubmed/24962785 http://dx.doi.org/10.1186/1472-6882-14-200 |
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author | Eo, Hyun Ji Park, Jae Ho Park, Gwang Hun Lee, Man Hyo Lee, Jeong Rak Koo, Jin Suk Jeong, Jin Boo |
author_facet | Eo, Hyun Ji Park, Jae Ho Park, Gwang Hun Lee, Man Hyo Lee, Jeong Rak Koo, Jin Suk Jeong, Jin Boo |
author_sort | Eo, Hyun Ji |
collection | PubMed |
description | BACKGROUND: Root bark of mulberry (Morus alba L.) has been used in herbal medicine as anti-phlogistic, liver protective, kidney protective, hypotensive, diuretic, anti-cough and analgesic agent. However, the anti-cancer activity and the potential anti-cancer mechanisms of mulberry root bark have not been elucidated. We performed in vitro study to investigate whether mulberry root bark extract (MRBE) shows anti-inflammatory and anti-cancer activity. METHODS: In anti-inflammatory activity, NO was measured using the griess method. iNOS and proteins regulating NF-κB and ERK1/2 signaling were analyzed by Western blot. In anti-cancer activity, cell growth was measured by MTT assay. Cleaved PARP, ATF3 and cyclin D1 were analyzed by Western blot. RESULTS: In anti-inflammatory effect, MRBE blocked NO production via suppressing iNOS over-expression in LPS-stimulated RAW264.7 cells. In addition, MRBE inhibited NF-κB activation through p65 nuclear translocation via blocking IκB-α degradation and ERK1/2 activation via its hyper-phosphorylation. In anti-cancer activity, MRBE deos-dependently induced cell growth arrest and apoptosis in human colorectal cancer cells, SW480. MRBE treatment to SW480 cells activated ATF3 expression and down-regulated cyclin D1 level. We also observed that MRBE-induced ATF3 expression was dependent on ROS and GSK3β. Moreover, MRBE-induced cyclin D1 down-regulation was mediated from cyclin D1 proteasomal degradation, which was dependent on ROS. CONCLUSIONS: These findings suggest that mulberry root bark exerts anti-inflammatory and anti-cancer activity. |
format | Online Article Text |
id | pubmed-4074313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40743132014-06-29 Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark Eo, Hyun Ji Park, Jae Ho Park, Gwang Hun Lee, Man Hyo Lee, Jeong Rak Koo, Jin Suk Jeong, Jin Boo BMC Complement Altern Med Research Article BACKGROUND: Root bark of mulberry (Morus alba L.) has been used in herbal medicine as anti-phlogistic, liver protective, kidney protective, hypotensive, diuretic, anti-cough and analgesic agent. However, the anti-cancer activity and the potential anti-cancer mechanisms of mulberry root bark have not been elucidated. We performed in vitro study to investigate whether mulberry root bark extract (MRBE) shows anti-inflammatory and anti-cancer activity. METHODS: In anti-inflammatory activity, NO was measured using the griess method. iNOS and proteins regulating NF-κB and ERK1/2 signaling were analyzed by Western blot. In anti-cancer activity, cell growth was measured by MTT assay. Cleaved PARP, ATF3 and cyclin D1 were analyzed by Western blot. RESULTS: In anti-inflammatory effect, MRBE blocked NO production via suppressing iNOS over-expression in LPS-stimulated RAW264.7 cells. In addition, MRBE inhibited NF-κB activation through p65 nuclear translocation via blocking IκB-α degradation and ERK1/2 activation via its hyper-phosphorylation. In anti-cancer activity, MRBE deos-dependently induced cell growth arrest and apoptosis in human colorectal cancer cells, SW480. MRBE treatment to SW480 cells activated ATF3 expression and down-regulated cyclin D1 level. We also observed that MRBE-induced ATF3 expression was dependent on ROS and GSK3β. Moreover, MRBE-induced cyclin D1 down-regulation was mediated from cyclin D1 proteasomal degradation, which was dependent on ROS. CONCLUSIONS: These findings suggest that mulberry root bark exerts anti-inflammatory and anti-cancer activity. BioMed Central 2014-06-25 /pmc/articles/PMC4074313/ /pubmed/24962785 http://dx.doi.org/10.1186/1472-6882-14-200 Text en Copyright © 2014 Eo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Eo, Hyun Ji Park, Jae Ho Park, Gwang Hun Lee, Man Hyo Lee, Jeong Rak Koo, Jin Suk Jeong, Jin Boo Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark |
title | Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark |
title_full | Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark |
title_fullStr | Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark |
title_full_unstemmed | Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark |
title_short | Anti-inflammatory and anti-cancer activity of mulberry (Morus alba L.) root bark |
title_sort | anti-inflammatory and anti-cancer activity of mulberry (morus alba l.) root bark |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4074313/ https://www.ncbi.nlm.nih.gov/pubmed/24962785 http://dx.doi.org/10.1186/1472-6882-14-200 |
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