Abstract |
Cimiside E was isolated from the Cimicifuga heracleifolia Komarov extract, which has been previously demonstrated to possess apoptotic action on gastric cancer cells. The IC(50) value of cimiside E on gastric cancer cells for 24 h was 14.58 microM. The mechanism of apoptosis was further elucidated through western blot, RT-PCR, morphology, Annexin V-FITC/PI staining and cell cycle analysis. Cell cycle arrest was induced by cimiside E in S phase at a lower concentration (30 microM) and G2/M phase at higher concentrations (60 and 90 microM). Cimiside E mediated apoptosis through the induction of the caspase cascade for both the extrinsic and intrinsic pathways. These findings suggest that cimiside E may be an effective chemopreventive agent against cancer.
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Authors | Lian Yu Guo, Eun Ji Joo, Kun Ho Son, Su Jin Jeon, Sehyun Jang, Eun Myoung Shin, Hong Yu Zhou, Yeong Shik Kim |
Journal | Archives of pharmacal research
(Arch Pharm Res)
Vol. 32
Issue 10
Pg. 1385-92
(Oct 2009)
ISSN: 0253-6269 [Print] Korea (South) |
PMID | 19898801
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Annexin A5
- Antineoplastic Agents, Phytogenic
- FAS protein, human
- FASLG protein, human
- Fas Ligand Protein
- Saponins
- Triterpenes
- cimiside E
- fas Receptor
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Topics |
- Annexin A5
(metabolism)
- Antineoplastic Agents, Phytogenic
(isolation & purification, pharmacology)
- Apoptosis
(drug effects)
- Blotting, Western
- Cell Cycle
(drug effects)
- Cell Line, Tumor
- Cell Proliferation
(drug effects)
- Cimicifuga
(chemistry)
- DNA Fragmentation
(drug effects)
- Fas Ligand Protein
(metabolism)
- Humans
- Reverse Transcriptase Polymerase Chain Reaction
- Saponins
(isolation & purification, pharmacology)
- Stomach Neoplasms
(pathology)
- Triterpenes
(isolation & purification, pharmacology)
- fas Receptor
(metabolism)
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