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  4. Effects of antioxidants and caspase-3 inhibitor on the phenylethyl isothiocyanate-induced apoptotic signaling pathways in human PLC/PRF/5 cells
 
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Effects of antioxidants and caspase-3 inhibitor on the phenylethyl isothiocyanate-induced apoptotic signaling pathways in human PLC/PRF/5 cells

Journal
European Journal of Pharmacology
Journal Volume
518
Journal Volume
518
Journal Issue
2-3
Journal Issue
2-3
Pages
96-106
Start Page
96
End Page
106
ISSN
00142999
Date Issued
2005-08-22
Author(s)
Wu, Shu-Jing
LEAN-TEIK HUANG  
Lin, Chun-Ching
DOI
10.1016/j.ejphar.2005.06.021
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-23644454249&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/314973
Abstract
Phenylethyl isothiocyanate (PEITC) is a well recognized potential chemopreventive compound against human cancers. In this study, the molecular mechanism of PEITC-induced apoptosis was examined with two antioxidants (N-acetyl-cysteine and vitamin E) and a caspase-3 inhibitor (z-DEVD-fmk). Results demonstrated that PEITC significantly induced human hepatoma PLC/PRF/5 (CD95-negative) cells undergoing apoptosis. Treatment with 0∼10 μM PEITC-triggered cell apoptosis as revealed by the externalization of annexin V-targeted phosphatidylserine and the subsequent appearance of sub-G1 population. Results also displayed that PEITC-induced apoptosis involves the up-regulation of p53 and Bax protein, down-regulation of the XIAP, Bcl-2, Bcl-XL and Mcl-1 proteins, cleavage of Bid, and the release of cytochrome c and Smac/Diablo, which were accompanied by the activation of caspases -9, -3 and -8. PEITC-induced the generation of reactive oxygen species and the decrease of mitochondrial membrane potential (Δψm) in a time-dependent pattern. N-acetyl-cysteine and vitamin E at 100 μM, and z-DEVD-fmk at 50 μM markedly blocked PEITC-induced apoptosis, which was demonstrated by a decline in the reactive oxygen species generation and the release of the cytochrome c and Smac/Diablo from mitochondria to the cytosol. N-acetyl-cysteine, vitamin E and z-DEVD-fmk also prevented the PEITC in inducing the loss of Δψm. They also affected the activity of XIAP and Bax proteins. Taken together, these studies suggest that PEITC is an apoptotic inducer that acts on the mitochondria and the feedback amplification loop of caspase-8/Bid pathways in PLC/PRF/5 cells.
Subjects
Antioxidant
Apoptosis
Caspase-3 inhibitor
Phenylethyl isothiocyanate
PLC/PRF/5 cell
Type
journal article

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