Caspase-8 acts as a key upstream executor of mitochondria during justicidin A-induced apoptosis in human hepatoma cells |
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Authors: | Su Chun-Li Huang Lynn L H Huang Li-Min Lee Jenq-Chang Lin Chun-Nan Won Shen-Jeu |
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Affiliation: | Department of Nursing, Chang Jung Christian University, Tainan 711, Taiwan. |
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Abstract: | Justicia procumbens is a traditional Taiwanese herbal remedy used to treat fever, pain, and cancer. Justicidin A, isolated from Justicia procumbens, has been reported to suppress in vitro growth of several tumor cell lines as well as hepatoma cells. In this study, justicidin A activated caspase-8 to increase tBid, disrupted mitochondrial membrane potential (Delta psi(m)), and caused the release of cytochrome c and Smac/DIABLO in Hep 3B and Hep G2 cells. Justicidin A also reduced Bcl-x(L) and increased Bax and Bak in mitochondria. Caspase-8 inhibitor (Z-IETD) attenuated the justicidin A-induced disruption of Delta psi(m). Growth of Hep 3B implanted in NOD-SCID mice was suppressed significantly by oral justicidin A (20 mg/kg/day). These results indicate that justicidin A-induced apoptosis in these cells proceeds via caspase-8 and is followed by mitochondrial disruption. |
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Keywords: | HCC, hepatocellular carcinoma PBMC, peripheral blood mononuclear cells Smac/DIABLO, second mitochondria-derived activator of caspase/direct IAP binding protein with low pI PARP, poly(ADP-ribose) polymerase DFF, DNA fragmentation factor Δψm, mitochondrial membrane potential XIAP, X-linked apoptosis-inhibiting protein MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide mAB, monoclonal antibody pAB, polyclonal antibody |
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