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CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways
CCM111 is an aqueous extract of Antrodia cinnamomea (AC) that has exhibited anti-liver fibrosis functions. However, the detailed mechanisms of AC action against liver fibrosis have not been elucidated yet. The present research showed that CCM111 significantly lowered the levels of the hepatic enzyme...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taiwan Food and Drug Administration
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298635/ https://www.ncbi.nlm.nih.gov/pubmed/30648571 http://dx.doi.org/10.1016/j.jfda.2018.09.008 |
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author | Lin, In-Yu Chiou, Yi-Shiou Wu, Li-Ching Tsai, Chen-Yu Chen, Chiung-Tong Chuang, Wu-Chang Lee, Ming-Chung Lin, Ching-Che Lin, Ting-Ting Chen, Ssu-Ching Pan, Min-Hsiung Ma, Nianhan |
author_facet | Lin, In-Yu Chiou, Yi-Shiou Wu, Li-Ching Tsai, Chen-Yu Chen, Chiung-Tong Chuang, Wu-Chang Lee, Ming-Chung Lin, Ching-Che Lin, Ting-Ting Chen, Ssu-Ching Pan, Min-Hsiung Ma, Nianhan |
author_sort | Lin, In-Yu |
collection | PubMed |
description | CCM111 is an aqueous extract of Antrodia cinnamomea (AC) that has exhibited anti-liver fibrosis functions. However, the detailed mechanisms of AC action against liver fibrosis have not been elucidated yet. The present research showed that CCM111 significantly lowered the levels of the hepatic enzyme markers glutamate oxaloacetate transaminase (GOT) and glutamic pyruvic transaminase (GPT), prevented liver damage and collagen deposition, and downregulated TGF-β/Smad signaling in a dose-dependent manner compared with CCl(4) treatment alone. CCM111 markedly inhibited TGF-β, Wnt and STAT3 signaling pathway-regulated downstream genes in the liver by next-generation sequencing. The antifibrotic mechanisms of CCM111 were further demonstrated in HSC-T6 cells. Our data demonstrated for the first time that CCM111 can protect against CCl(4)-induced liver fibrosis by the cooperative inhibition of TGF-β-, Wnt- and STAT3-dependent proinflammatory and profibrotic mediators, suggesting that CCM111 might be a candidate for preventing and treating chronic fibrotic liver diseases. |
format | Online Article Text |
id | pubmed-9298635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taiwan Food and Drug Administration |
record_format | MEDLINE/PubMed |
spelling | pubmed-92986352022-08-09 CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways Lin, In-Yu Chiou, Yi-Shiou Wu, Li-Ching Tsai, Chen-Yu Chen, Chiung-Tong Chuang, Wu-Chang Lee, Ming-Chung Lin, Ching-Che Lin, Ting-Ting Chen, Ssu-Ching Pan, Min-Hsiung Ma, Nianhan J Food Drug Anal Original Article CCM111 is an aqueous extract of Antrodia cinnamomea (AC) that has exhibited anti-liver fibrosis functions. However, the detailed mechanisms of AC action against liver fibrosis have not been elucidated yet. The present research showed that CCM111 significantly lowered the levels of the hepatic enzyme markers glutamate oxaloacetate transaminase (GOT) and glutamic pyruvic transaminase (GPT), prevented liver damage and collagen deposition, and downregulated TGF-β/Smad signaling in a dose-dependent manner compared with CCl(4) treatment alone. CCM111 markedly inhibited TGF-β, Wnt and STAT3 signaling pathway-regulated downstream genes in the liver by next-generation sequencing. The antifibrotic mechanisms of CCM111 were further demonstrated in HSC-T6 cells. Our data demonstrated for the first time that CCM111 can protect against CCl(4)-induced liver fibrosis by the cooperative inhibition of TGF-β-, Wnt- and STAT3-dependent proinflammatory and profibrotic mediators, suggesting that CCM111 might be a candidate for preventing and treating chronic fibrotic liver diseases. Taiwan Food and Drug Administration 2018-10-25 /pmc/articles/PMC9298635/ /pubmed/30648571 http://dx.doi.org/10.1016/j.jfda.2018.09.008 Text en © 2019 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Original Article Lin, In-Yu Chiou, Yi-Shiou Wu, Li-Ching Tsai, Chen-Yu Chen, Chiung-Tong Chuang, Wu-Chang Lee, Ming-Chung Lin, Ching-Che Lin, Ting-Ting Chen, Ssu-Ching Pan, Min-Hsiung Ma, Nianhan CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways |
title | CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways |
title_full | CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways |
title_fullStr | CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways |
title_full_unstemmed | CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways |
title_short | CCM111 prevents hepatic fibrosis via cooperative inhibition of TGF-β, Wnt and STAT3 signaling pathways |
title_sort | ccm111 prevents hepatic fibrosis via cooperative inhibition of tgf-β, wnt and stat3 signaling pathways |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298635/ https://www.ncbi.nlm.nih.gov/pubmed/30648571 http://dx.doi.org/10.1016/j.jfda.2018.09.008 |
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