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Research ArticleExperimental Studies

Synergistic Cell Death by EGCG and Ibuprofen in DU-145 Prostate Cancer Cell Line

MYOUNG H. KIM and JAEGWON CHUNG
Anticancer Research November 2007, 27 (6B) 3947-3956;
MYOUNG H. KIM
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  • For correspondence: mkim{at}hsc.unt.edu
JAEGWON CHUNG
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Abstract

Background: One of the green tea components epigallocatechin-3-gallate (EGCG) significantly prevented the growth of prostate cancer cells. In this study, synergistic effect of EGCG and ibuprofen (EGCG+ibuprofen) was investigated to determine their anti-proliferative and pro-apoptotic action in DU-145 prostate cancer cells. Materials and Methods: Cell death analysis, immunoblotting, RT-PCR analysis, and caspase activity assay were used. Results: EGCG+ibuprofen treatment resulted in 90% growth inhibition, while ibuprofen or EGCG alone reduced cell numbers by 25% and 20%, respectively. EGCG+ibuprofen induced MAPK activation, caspase activation and the inhibition of Bfl-1 expression, all of which were blocked by the antioxidant, N-acetyl-L-cysteine (NAC). Moreover, addition of ceramide rescued the NAC-inhibited MAPK activation and pretreatment with the ceramide synthase inhibitor, fumonisin B1, reduced cell death. Conclusion: Our results suggest that in DU-145 prostate cancer cells: (i) EGCG+ibuprofen treatment has a synergistic effect on apoptosis, and (ii) oxidative stress, directly or indirectly via ceramide synthesis mediates pro-apoptotic signaling.

  • Prostate cancer
  • EGCG
  • ibuprofen
  • ceramide
  • apoptosis

Footnotes

  • Received March 8, 2007.
  • Revision received June 21, 2007.
  • Accepted July 23, 2007.
  • Copyright© 2007 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved
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Vol. 27, Issue 6B
November-December 2007
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Synergistic Cell Death by EGCG and Ibuprofen in DU-145 Prostate Cancer Cell Line
MYOUNG H. KIM, JAEGWON CHUNG
Anticancer Research Nov 2007, 27 (6B) 3947-3956;

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Synergistic Cell Death by EGCG and Ibuprofen in DU-145 Prostate Cancer Cell Line
MYOUNG H. KIM, JAEGWON CHUNG
Anticancer Research Nov 2007, 27 (6B) 3947-3956;
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