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Induction of apoptosis by Chan Su, a traditional Chinese medicine, in human bladder carcinoma T24 cells.

Abstract
Chan Su is a traditional Chinese medicine prepared from the dried white secretion of the auricular and skin glands of toads, and has been used as an Oriental drug. However, little is known about the effect of Chan Su on the growth of human cancer cells. This study was undertaken to investigate the underlying mechanism of Chan Su-induced apoptosis in a human bladder carcinoma cell line, T24. The effects of this compound were also tested on cyclooxygenase (COX) activity. Treatment of T24 cells with Chan Su resulted in the inhibition of viability and induction of apoptosis in a concentration-dependent manner, which was proved by trypan blue counts, DAPI staining, agarose gel electrophoresis and flow cytometric analysis. Apoptosis of T24 cells by Chan Su was associated with a down-regulation of anti-apoptotic Bcl-2 and Bcl-X(S/L) expression and an up-regulation of pro-apoptotic Bax expression. Chan Su treatment induced the proteolytic activation of caspase-3 and caspase-9, and a concomitant degradation of poly(ADP-ribose)-polymerase and beta-catenin protein. Furthermore, Chan Su decreased the levels of COX-2 mRNA and protein expression without significant changes in the levels of COX-1, which was correlated with an inhibition in prostaglandin E(2) synthesis. Taken together, these findings partially provide novel insights into the possible molecular mechanisms of the anti-cancer activity of Chan Su.
AuthorsWoo Shin Ko, Tae Yeol Park, Cheol Park, Young Hee Kim, Hwa Jung Yoon, Seung Yeon Lee, Sang Hoon Hong, Byung Tae Choi, Yong Tae Lee, Yung Hyun Choi
JournalOncology reports (Oncol Rep) Vol. 14 Issue 2 Pg. 475-80 (Aug 2005) ISSN: 1021-335X [Print] Greece
PMID16012733 (Publication Type: Journal Article)
Chemical References
  • Amphibian Venoms
  • BAX protein, human
  • BCL2L1 protein, human
  • Bufanolides
  • CTNNB1 protein, human
  • Cytoskeletal Proteins
  • Membrane Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • Trans-Activators
  • bcl-2-Associated X Protein
  • bcl-X Protein
  • beta Catenin
  • chan su
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • PTGS1 protein, human
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Poly(ADP-ribose) Polymerases
  • CASP3 protein, human
  • CASP9 protein, human
  • Caspase 3
  • Caspase 9
  • Caspases
  • Dinoprostone
Topics
  • Amphibian Venoms (pharmacology)
  • Animals
  • Apoptosis (drug effects)
  • Blotting, Western
  • Bufanolides (pharmacology)
  • Caspase 3
  • Caspase 9
  • Caspases (metabolism)
  • Cell Line, Tumor
  • Cell Proliferation (drug effects)
  • Cell Survival (drug effects)
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Cytoskeletal Proteins (metabolism)
  • Dinoprostone (metabolism)
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation, Neoplastic (drug effects)
  • Humans
  • Immunoenzyme Techniques
  • Membrane Proteins
  • Poly(ADP-ribose) Polymerases (metabolism)
  • Prostaglandin-Endoperoxide Synthases (genetics, metabolism)
  • Proto-Oncogene Proteins c-bcl-2 (genetics, metabolism)
  • Reverse Transcriptase Polymerase Chain Reaction
  • Trans-Activators (metabolism)
  • Urinary Bladder Neoplasms (genetics, metabolism, pathology)
  • bcl-2-Associated X Protein
  • bcl-X Protein
  • beta Catenin

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