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Cimiside E arrests cell cycle and induces cell apoptosis in gastric cancer cells.

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.
AuthorsLian Yu Guo, Eun Ji Joo, Kun Ho Son, Su Jin Jeon, Sehyun Jang, Eun Myoung Shin, Hong Yu Zhou, Yeong Shik Kim
JournalArchives of pharmacal research (Arch Pharm Res) Vol. 32 Issue 10 Pg. 1385-92 (Oct 2009) ISSN: 0253-6269 [Print] Korea (South)
PMID19898801 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Annexin A5
  • Antineoplastic Agents, Phytogenic
  • FAS protein, human
  • FASLG protein, human
  • Fas Ligand Protein
  • Saponins
  • Triterpenes
  • cimiside E
  • fas Receptor
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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