Arsenic Trioxide Induces Apoptosis of HL-60 Cells via Activation of Intrinsic Caspase Protease with Mitochondrial Dysfunction.
- Author:
Byung Hak JUNG
1
;
Channy PARK
;
Hak Ryul KIM
;
Moo Rim PARK
Author Information
1. Department of Internal Medicine, School of Medicine, Wonkwang University, Iksan, Korea.
- Publication Type:Multicenter Study ; Original Article
- Keywords:
Arsenic trioxide;
Apoptosis;
Caspase
- MeSH:
Apoptosis*;
Arsenic*;
Caspase 3;
China;
Chromatin;
Cysteine Proteases;
DNA Fragmentation;
HL-60 Cells*;
Humans;
Leukemia, Promyelocytic, Acute;
Membrane Potential, Mitochondrial;
Peptide Hydrolases;
Strikes, Employee;
United States
- From:Cancer Research and Treatment
2002;34(4):308-315
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Arsenic trioxide (As2O3) was introduced into the treatment of refractory or relapsed acute promyelocytic leukemia and showed a striking effectiveness in China and United States multicenter study. However, the mechanistic basis for the carcinogenic or therapeutic effects of arsenics is still poorly understood. So, this study is performed to determine whether As2O3 induces apoptosis through intrinsic caspase cascades in acute promyelocytic leukemia HL-60 cells. MATERIALS AND METHODS: HL-60 cells were treated with As2O3 to investigate apoptosis through signaling of caspase cascades and mitochondrial dysfunction. RESULTS: As2O3 (>0.5 uM) decreased the viability of HL-60 cells in a dose-dependent manner, which was revealed as apoptosis shown chromatin condensation and ladder pattern DNA fragmentation. As2O3 increased the catalytic activity of caspase family cysteine proteases including caspase-3 and -9 proteases. Consistently, PARP, an intracellular biosubstrate of caspase-3 protease, was cleaved from 116 kDa to 85 kDa fragments. It also induced the change of mitochondrial membrane potential. Morever, As2O3 resulted in the increase of Bak. CONCLUSION: These data suggest that As2O3 induces apoptosis of HL-60 cells through activation of intrinsic caspase protease with mitochondrial dysfunction.
