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[Mechanism of apoptosis induced by specific COX-2 inhibitor SC236 in gastric cancer cells].

AbstractOBJECTIVE:
To investigate the underlying mechanism of apoptosis-inducing effect of a specific COX-2 inhibitor SC236 in gastric cancer cells.
METHODS:
Western blot analysis was used to measure apoptosis-related proteins, cytochrome c, and caspase-3. The catalytic activity of the caspases was measured using a colorimetric assay.
RESULTS:
Treatment of AGS gastric cancer cells with SC236 caused a significant elevation of the pro-apoptotic protein Bak, release of cytochrome c to the cytosol, and activation of caspase-3. A specific caspase-3 inhibitor, z-DEVD-fmk, blocked SC236-induced apoptosis.
CONCLUSION:
SC236 inhibits cell growth and induces apoptosis in gastric cancer cells at least partly through the up-regulation of Bak, stimulation of cytochrome c release, and activation of caspase-3.
AuthorsXiao-ming Fan, Fa-shou Zheng, Hong-yan Liu, Yuan-hua Ma, B C Y Wong
JournalZhonghua zhong liu za zhi [Chinese journal of oncology] (Zhonghua Zhong Liu Za Zhi) Vol. 27 Issue 3 Pg. 145-7 (Mar 2005) ISSN: 0253-3766 [Print] China
PMID15946562 (Publication Type: English Abstract, Journal Article)
Chemical References
  • 4-(5-(4-chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)benzenesulfonamide
  • Cyclooxygenase 2 Inhibitors
  • Oligopeptides
  • Pyrazoles
  • Sulfonamides
  • bcl-2 Homologous Antagonist-Killer Protein
  • benzoylcarbonyl-aspartyl-glutamyl-valyl-aspartyl-fluoromethyl ketone
  • Cytochromes c
  • Poly(ADP-ribose) Polymerases
  • CASP3 protein, human
  • Caspase 3
  • Caspases
Topics
  • Adenocarcinoma (metabolism, pathology)
  • Apoptosis (drug effects)
  • Caspase 3
  • Caspases (metabolism)
  • Cell Line, Tumor
  • Cyclooxygenase 2 Inhibitors (pharmacology)
  • Cytochromes c (metabolism)
  • Humans
  • Oligopeptides (pharmacology)
  • Poly(ADP-ribose) Polymerases (metabolism)
  • Pyrazoles (pharmacology)
  • Stomach Neoplasms (metabolism, pathology)
  • Sulfonamides (pharmacology)
  • bcl-2 Homologous Antagonist-Killer Protein (metabolism)

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