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;