TY - JOUR T1 - Induction of apoptosis by Meretrix lusoria through reactive oxygen species production, glutathione depletion, and caspase activation in human leukemia cells. AU - Pan,Min-Hsiung, AU - Huang,Yu-Ting, AU - Ho,Chi-Tang, AU - Chang,Chi-I, AU - Hsu,Ping-Chi, AU - Sun Pan,Bonnie, Y1 - 2006/04/26/ PY - 2005/11/13/received PY - 2006/03/13/revised PY - 2006/03/13/accepted PY - 2006/5/30/pubmed PY - 2006/9/14/medline PY - 2006/5/30/entrez SP - 1140 EP - 52 JF - Life sciences JO - Life Sci VL - 79 IS - 12 N2 - Apoptosis-induced directed fractionation and purification was used to identify the bioactive components of hard clams (HC), Meretrix lusoria. Two stereoisomers of epidioxysterol were previously identified as the active compounds in the ethyl acetate fraction (HC-EA). The molecular mechanism of HC-EA-induced apoptosis was also investigated in this study. Dissipation of mitochondrial membrane potential, release of mitochondrial cytochrome c into cytosol, and subsequent induction of pro-caspase-9 and -3 processing preceded apoptosis in HL-60 cells, confirmed by DNA fragmentation, chromatin condensation, changes in the cell membrane and the appearance of a sub-G1 DNA peak. Furthermore, treatment with HC-EA caused a rapid loss of intracellular glutathione content and stimulation of reactive oxygen species (ROS). Antioxidants such as catalase, N-acetylcysteine, pyrrolidine dithiocarbamate, and superoxide dismutase, but not allopurinol and diphenylene iodonium, significantly inhibited HC-EA-induced cell death. Apoptosis was completely prevented by a pan-caspase inhibitor, z-Val-Ala-Asp-fluoromethyl ketone (z-VAD-FMK). The induction of apoptosis by M. lusoria may prove to be a pivotal mechanism for its cancer chemopreventive action. SN - 0024-3205 UR - https://www.unboundmedicine.com/medline/citation/16730358/Induction_of_apoptosis_by_Meretrix_lusoria_through_reactive_oxygen_species_production_glutathione_depletion_and_caspase_activation_in_human_leukemia_cells_ DB - PRIME DP - Unbound Medicine ER -