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Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways

Antcin-H, a natural triterpene, is purified from a famous anticancer medicinal mushroom, Antrodia cinnamomea, in Taiwan. This study showed that antcin-H inhibited the growth of human renal carcinoma 786-0 cells; the IC(50) value (for 48 h) was 170 μM. Besides, the migration and invasion of 786-0 cel...

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Autores principales: Chiu, Kun-Yuan, Chen, Tzu-Hsiu, Wen, Chi-Luan, Lai, Jin-Mei, Cheng, Chi-Chih, Liu, Hsiang-Chun, Hsu, Shih-Lan, Tzeng, Yew-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688354/
https://www.ncbi.nlm.nih.gov/pubmed/29234409
http://dx.doi.org/10.1155/2017/5052870
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author Chiu, Kun-Yuan
Chen, Tzu-Hsiu
Wen, Chi-Luan
Lai, Jin-Mei
Cheng, Chi-Chih
Liu, Hsiang-Chun
Hsu, Shih-Lan
Tzeng, Yew-Min
author_facet Chiu, Kun-Yuan
Chen, Tzu-Hsiu
Wen, Chi-Luan
Lai, Jin-Mei
Cheng, Chi-Chih
Liu, Hsiang-Chun
Hsu, Shih-Lan
Tzeng, Yew-Min
author_sort Chiu, Kun-Yuan
collection PubMed
description Antcin-H, a natural triterpene, is purified from a famous anticancer medicinal mushroom, Antrodia cinnamomea, in Taiwan. This study showed that antcin-H inhibited the growth of human renal carcinoma 786-0 cells; the IC(50) value (for 48 h) was 170 μM. Besides, the migration and invasion of 786-0 cells were suppressed by antcin-H under noncytotoxic concentrations (<100 μM); these events were accompanied by inhibition of FAK and Src kinase activities, decrease of paxillin phosphorylation, impairment of lamellipodium formation, and upregulation of TIMPs and downregulation of MMPs, especially MMP-7 expression. Luciferase reporter assay showed that antcin-H repressed the MMP-7 promoter activity, in parallel to inhibiting c-Fos/AP-1 and C/EBP-β transactivation abilities. Moreover, antcin-H suppressed the activity of ERK1/2 and decreased the binding ability of C/EBP-β and c-Fos on the upstream/enhancer region of MMP-7 promoter. Overall, this study demonstrated that the anti-invasive effect of antcin-H in human renal carcinoma 786-0 cells might be at least in part by abrogating focal adhesion complex and lamellipodium formation through inhibiting the Src/FAK-paxillin signaling pathways and decreasing MMP-7 expression through suppressing the ERK1/2-AP-1/c-Fos and C/EBP-β signaling axis. Our findings provide the evidence that antcin-H may be an active component existing in A. cinnamomea with anticancer effect.
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spelling pubmed-56883542017-12-11 Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways Chiu, Kun-Yuan Chen, Tzu-Hsiu Wen, Chi-Luan Lai, Jin-Mei Cheng, Chi-Chih Liu, Hsiang-Chun Hsu, Shih-Lan Tzeng, Yew-Min Evid Based Complement Alternat Med Research Article Antcin-H, a natural triterpene, is purified from a famous anticancer medicinal mushroom, Antrodia cinnamomea, in Taiwan. This study showed that antcin-H inhibited the growth of human renal carcinoma 786-0 cells; the IC(50) value (for 48 h) was 170 μM. Besides, the migration and invasion of 786-0 cells were suppressed by antcin-H under noncytotoxic concentrations (<100 μM); these events were accompanied by inhibition of FAK and Src kinase activities, decrease of paxillin phosphorylation, impairment of lamellipodium formation, and upregulation of TIMPs and downregulation of MMPs, especially MMP-7 expression. Luciferase reporter assay showed that antcin-H repressed the MMP-7 promoter activity, in parallel to inhibiting c-Fos/AP-1 and C/EBP-β transactivation abilities. Moreover, antcin-H suppressed the activity of ERK1/2 and decreased the binding ability of C/EBP-β and c-Fos on the upstream/enhancer region of MMP-7 promoter. Overall, this study demonstrated that the anti-invasive effect of antcin-H in human renal carcinoma 786-0 cells might be at least in part by abrogating focal adhesion complex and lamellipodium formation through inhibiting the Src/FAK-paxillin signaling pathways and decreasing MMP-7 expression through suppressing the ERK1/2-AP-1/c-Fos and C/EBP-β signaling axis. Our findings provide the evidence that antcin-H may be an active component existing in A. cinnamomea with anticancer effect. Hindawi 2017 2017-11-02 /pmc/articles/PMC5688354/ /pubmed/29234409 http://dx.doi.org/10.1155/2017/5052870 Text en Copyright © 2017 Kun-Yuan Chiu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chiu, Kun-Yuan
Chen, Tzu-Hsiu
Wen, Chi-Luan
Lai, Jin-Mei
Cheng, Chi-Chih
Liu, Hsiang-Chun
Hsu, Shih-Lan
Tzeng, Yew-Min
Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways
title Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways
title_full Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways
title_fullStr Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways
title_full_unstemmed Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways
title_short Antcin-H Isolated from Antrodia cinnamomea Inhibits Renal Cancer Cell Invasion Partly through Inactivation of FAK-ERK-C/EBP-β/c-Fos-MMP-7 Pathways
title_sort antcin-h isolated from antrodia cinnamomea inhibits renal cancer cell invasion partly through inactivation of fak-erk-c/ebp-β/c-fos-mmp-7 pathways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688354/
https://www.ncbi.nlm.nih.gov/pubmed/29234409
http://dx.doi.org/10.1155/2017/5052870
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