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.
Kun-Yuan ChiuTzu-Hsiu ChenChi-Luan WenJin-Mei LaiChi-Chih ChengHsiang-Chun LiuShih-Lan HsuYew-Min TzengPublished in: Evidence-based complementary and alternative medicine : eCAM (2017)
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 IC50 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.
Keyphrases
- signaling pathway
- cell migration
- induced apoptosis
- pi k akt
- transcription factor
- poor prognosis
- cell proliferation
- endothelial cells
- epithelial mesenchymal transition
- binding protein
- dna methylation
- cell cycle arrest
- tyrosine kinase
- gene expression
- protein kinase
- induced pluripotent stem cells
- squamous cell carcinoma
- oxidative stress
- cystic fibrosis
- pseudomonas aeruginosa
- squamous cell
- cell death