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Cited 23 time in webofscience Cited 23 time in scopus
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Rhus verniciflua Extract Modulates Survival of MCF-7 Breast Cancer Cells through the Modulation of AMPK-Pathwayopen access

Authors
Lee, Jung OkMoon, Ji WookLee, Soo KyungKim, So MiKim, NamiKo, Seong-GyuKim, Hyeon SooPark, Sun Hwa
Issue Date
May-2014
Publisher
Pharmaceutical Society of Japan
Keywords
Rhus verniciflua; AMP-activated protein kinase (AMPK); apoptosis; MCF-7
Citation
Biological and Pharmaceutical Bulletin, v.37, no.5, pp 794 - 801
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
Biological and Pharmaceutical Bulletin
Volume
37
Number
5
Start Page
794
End Page
801
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/9378
DOI
10.1248/bpb.b13-00893
ISSN
0918-6158
1347-5215
Abstract
Rhus verniciflua STOKES (RVS) is used as an anti-cancer agent in traditional herbal medicine. However, the underlying molecular mechanism of its action is poorly understood. Here, we elucidated the mechanism of the anti-cancer mechanism of RVS in MCF-7 human breast cancer cells. We found that RVS increased the phosphorylation of AMP-activated protein kinase (AMPK) and downstream acetyl-CoA carboxylase (ACC) and suppressed cell viability in an AMPK-dependent fashion. RVS also induced an increase in reactive oxygen species (ROS) levels. RVS-induced AMPK phosphorylation was not observed in the presence of N-acetyl-cysteine (NAC), which indicated that ROS is associated with RVS-induced AMPK phosphorylation. In addition, fluorescent staining (Annexin V/propidium iodide) revealed that RVS increased the expression of Annexin V, which indicates that RVS leads to cancer-induced apoptosis. Moreover, RVS increased the phosphorylation of p53 and the expression of Bax. The inhibition of AMPK blocked RVS-induced p53 phosphorylation and Bax expression, which suggests that AMPK is involved in RVS-induced cancer apoptosis. Taken together, these results demonstrate that RVS has anti-tumor effects on MCF-7 cells through an AMPK-signaling pathway.
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3. Graduate School > Graduate School > 1. Journal Articles
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