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Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling
As a traditional anti-inflammatory Chinese herbal medicine, Alkaloid berberine has been recently reported to exhibit anti-tumour effects against a wide spectrum of cancer. However, the mechanism was largely unknown. Gene chip array reveals that with berberine treatment, c-Myc, the target gene of Wnt...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117561/ https://www.ncbi.nlm.nih.gov/pubmed/24015932 http://dx.doi.org/10.1111/jcmm.12119 |
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author | Zhang, Junfang Cao, Hailong Zhang, Bing Cao, Hanwei Xu, Xiuqin Ruan, Hang Yi, Tingting Tan, Li Qu, Rui Song, Gang Wang, Bangmao Hu, Tianhui |
author_facet | Zhang, Junfang Cao, Hailong Zhang, Bing Cao, Hanwei Xu, Xiuqin Ruan, Hang Yi, Tingting Tan, Li Qu, Rui Song, Gang Wang, Bangmao Hu, Tianhui |
author_sort | Zhang, Junfang |
collection | PubMed |
description | As a traditional anti-inflammatory Chinese herbal medicine, Alkaloid berberine has been recently reported to exhibit anti-tumour effects against a wide spectrum of cancer. However, the mechanism was largely unknown. Gene chip array reveals that with berberine treatment, c-Myc, the target gene of Wnt pathway, was down-regulated 5.3-folds, indicating that berberine might inhibit Wnt signalling. TOPflash analysis revealed that Wnt activity was significantly reduced after berberine treatment, and the mechanism of which might be that berberine disrupted β-catenin transfer to nucleus through up-regulating the expression of adenomatous polyposis coli (APC) gene and stabilized APC-β-catenin complex. Berberine administration in ApcMin/+ mice exhibited fewer and smaller polyps in intestine, along with reduction in cyclin D1 and c-Myc expression. In clinical practice, oral administration of berberine also significantly reduced the familial adenomatous polyposis patients' polyp size along with the inhibition of cyclin D1 expression in polyp samples. These observations indicate that berberine inhibits colon tumour formation through inhibition of Wnt/β-catenin signalling and berberine might be a promising drug for the prevention of colon cancer. |
format | Online Article Text |
id | pubmed-4117561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | John Wiley & Sons |
record_format | MEDLINE/PubMed |
spelling | pubmed-41175612014-12-03 Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling Zhang, Junfang Cao, Hailong Zhang, Bing Cao, Hanwei Xu, Xiuqin Ruan, Hang Yi, Tingting Tan, Li Qu, Rui Song, Gang Wang, Bangmao Hu, Tianhui J Cell Mol Med Original Articles As a traditional anti-inflammatory Chinese herbal medicine, Alkaloid berberine has been recently reported to exhibit anti-tumour effects against a wide spectrum of cancer. However, the mechanism was largely unknown. Gene chip array reveals that with berberine treatment, c-Myc, the target gene of Wnt pathway, was down-regulated 5.3-folds, indicating that berberine might inhibit Wnt signalling. TOPflash analysis revealed that Wnt activity was significantly reduced after berberine treatment, and the mechanism of which might be that berberine disrupted β-catenin transfer to nucleus through up-regulating the expression of adenomatous polyposis coli (APC) gene and stabilized APC-β-catenin complex. Berberine administration in ApcMin/+ mice exhibited fewer and smaller polyps in intestine, along with reduction in cyclin D1 and c-Myc expression. In clinical practice, oral administration of berberine also significantly reduced the familial adenomatous polyposis patients' polyp size along with the inhibition of cyclin D1 expression in polyp samples. These observations indicate that berberine inhibits colon tumour formation through inhibition of Wnt/β-catenin signalling and berberine might be a promising drug for the prevention of colon cancer. John Wiley & Sons 2013-11 2013-09-09 /pmc/articles/PMC4117561/ /pubmed/24015932 http://dx.doi.org/10.1111/jcmm.12119 Text en Copyright © 2013 John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Zhang, Junfang Cao, Hailong Zhang, Bing Cao, Hanwei Xu, Xiuqin Ruan, Hang Yi, Tingting Tan, Li Qu, Rui Song, Gang Wang, Bangmao Hu, Tianhui Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling |
title | Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling |
title_full | Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling |
title_fullStr | Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling |
title_full_unstemmed | Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling |
title_short | Berberine potently attenuates intestinal polyps growth in ApcMin mice and familial adenomatous polyposis patients through inhibition of Wnt signalling |
title_sort | berberine potently attenuates intestinal polyps growth in apcmin mice and familial adenomatous polyposis patients through inhibition of wnt signalling |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117561/ https://www.ncbi.nlm.nih.gov/pubmed/24015932 http://dx.doi.org/10.1111/jcmm.12119 |
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