Pyrogallol inhibits the growth of lung cancer Calu-6 cells via caspase-dependent apoptosis |
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Authors: | Yong Hwan Han |
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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 |
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Abstract: | Pyrogallol (PG) is a polyphenol compound and a known O2− 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. |
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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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