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Pyrogallol inhibits the growth of lung cancer Calu-6 cells via caspase-dependent apoptosis
Authors:Yong Hwan Han
Affiliation:Department of Physiology, Medical School, Centers for Healthcare Technology Development, Institute for Medical Sciences, Chonbuk National University, san 2-20 Geumam-dong, Deokjin-gu, JeonJu 561-180, Republic of Korea
Abstract:
Pyrogallol (PG) is a polyphenol compound and a known O2radical dot generator. We evaluated the effects of PG on the growth and apoptosis of human pulmonary adenocarcinoma Calu-6 cells. PG decreased the viability of Calu-6 cells in a dose- and time-dependent manner. The induction of apoptosis by PG was accompanied by the loss of mitochondrial membrane potential (ΔΨm), cytochrome c release from mitochondria and activation of caspase-3 and caspase-8. All tested caspase inhibitors, especially the pan-caspase inhibitor (Z-VAD), markedly rescued Calu-6 cells from PG-induced cell death. Rescue was accompanied by inhibition of caspase-3 activation and PARP cleavage. Treatment with Z-VAD also prevented the loss of mitochondrial membrane potential (ΔΨm). In conclusion, PG inhibits the growth of Calu-6 cells via caspase-dependent apoptosis.
Keywords:PG, pyrogallol   ROS, reactive oxygen species   PARP, poly(ADP-ribose) polymerase   FBS, fetal bovine serum   MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide   PI, propidium iodide   FITC, fluorescein isothiocyanate   DAPI, 4&prime  -6-diamidino-2-phenylindole   Z-VAD-FMK, benzyloxycarbonyl-Val-Ala-Asp-fluoromethylketon   Z-DEVD-FMK, benzyloxycarbonyl-Asp-Glu-Val-Asp-fluoromethylketon   Z-IETD-FMK, benzyloxycarbonyl-Ile-Glu-Thr-Asp-fluoromethylketon   Z-LEHD-FMK, benzyloxycarbonyl-Leu-Glu-His-Asp-fluoromethylketon   NADPH, nicotine adenine diphosphate   SOD, superoxide dismutase   XO, xanthine oxidase   GSH, glutathione
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