• DocumentCode
    2088131
  • Title

    Ursolic Acid Accelerates Taxol-induced Apoptosis via Activation of Bid-Mitochondria-Cyto c Signaling Pathway

  • Author

    Li, Yunlong ; Da Xing

  • Author_Institution
    South China Normal Univ., Guangzhou
  • fYear
    2007
  • fDate
    23-27 May 2007
  • Firstpage
    984
  • Lastpage
    988
  • Abstract
    Taxol triggers apoptosis in a variety of cancer cell types and activated NF-KB is regarded as a main reason to cancer cells resistance to Taxol-induced apoptosis. Ursolic acid, a natural component, can inhibit activation of NF-KB in many apoptosis stimulus, such as TNF, cispatin. In order to find synergistic effect between Taxol and ursolic acid, plasmid pFRET-Bid, pE-GFP-Cyt-c, and pDsRed-Mit were used to dynamically monitor cleavage of Bid, and cytochrome c release from mitochondria in Taxol alone and combination treatment of Taxol and ursolic acid. In Taxol alone, Bid was not cleaved and cytochrome c was not released from mitochondria in ASTC-a-1 cells, however, cleavage of Bid and release of cytochrome c from mitochondria were observed in combination treatment of Taxol and ursolic acid, so we predicted that activation of Bid-Mitochodria-Cyto c signaling pathway might contribute to the enhancement of Taxol-induced apoptosis with ursolic acid during combination treatment. Furthermore, Taxol-induced apoptosis in ASTC-a-1 cells may be mainly dependent on intrinsic apoptosis pathway, and mitochondria may mediate apoptosis speed.
  • Keywords
    cancer; cellular biophysics; drugs; organic compounds; patient treatment; ASTC-a-1 cells; Bid cleavage; Bid-Mitochondria-Cyto c signaling; NF-KB; TNF; Taxol-induced apoptosis; cancer cell; cispatin; cytochrome c release; pDsRed-Mit; pE-GFP-Cyt-c; plasmid pFRET-Bid; ursolic acid; Acceleration; Biomedical engineering; Biomedical imaging; Cervical cancer; Drugs; Immune system; Laboratories; Laser theory; Monitoring; Neoplasms;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Complex Medical Engineering, 2007. CME 2007. IEEE/ICME International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-1077-4
  • Electronic_ISBN
    978-1-4244-1078-1
  • Type

    conf

  • DOI
    10.1109/ICCME.2007.4381887
  • Filename
    4381887