Induction of apoptosis by cordycepin via reactive oxygen species generation in human leukemia cells |
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Authors: | Jin-Woo Jeong Cheng-Yun Jin Cheol ParkSu Hyun Hong Gi-Young KimYong Kee Jeong Jae-Dong LeeYoung Hyun Yoo Yung Hyun Choi |
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Affiliation: | a Department of Biochemistry and Research Institute of Oriental Medicine, Dongeui University College of Oriental Medicine, Busan 614-052, Republic of Korea b Department of Microbiology, College of Natural Sciences, Pusan National University, Busan 609-735, Republic of Korea c Department of Biomaterial Control (BK21 Program), Dongeui University Graduate School, Busan 614-714, Republic of Korea d Blue-Bio Industry Regional Innovation Center, Dongeui University, Busan 614-714, Republic of Korea e Faculty of Applied Marine Science, Cheju National University, Jeju 690-756, Republic of Korea f Department of Biotechnology, College of Natural Resources and Life Science, Dong-A University, Busan 604-714, Republic of Korea g Department of Anatomy and Cell Biology, Dong-A University College of Medicine and Mitochondria Hub Regulation Center, Busan 602-714, Republic of Korea |
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Abstract: | ![]() Cordycepin (3′-deoxyadenosin), a specific polyadenylation inhibitor, is the main functional component in Cordyceps militaris, one of the top three renowned traditional Chinese medicines. Cordycepin has been shown to possess many pharmacological activities including immunological stimulation, and anti-bacterial, anti-viral, and anti-tumor effects. However, the mechanisms underlying its anti-cancer mechanisms are not yet understood. In this study, the apoptotic effects of cordycepin were investigated in human leukemia cells. Treatment with cordycepin significantly inhibited cell growth in a concentration-dependent manner by inducing apoptosis but not necrosis. This induction was associated with generation of reactive oxygen species (ROS), mitochondrial dysfunction, activation of caspases, and cleavage of poly(ADP-ribose) polymerase protein. However, apoptosis induced by cordycepin was attenuated by caspase inhibitors, indicating an important role for caspases in cordycepin responses. Administration of N-acetyl-l-cysteine, a scavenger of ROS, also significantly inhibited cordycepin-induced apoptosis and activation of caspases. These results support a mechanism whereby cordycepin induces apoptosis of human leukemia cells through a signaling cascade involving a ROS-mediated caspase pathway. |
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Keywords: | DCF-DA, 2&prime ,7&prime -dichlorofluorescein diacetate MTT, 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide DAPI, 4,6-diamidino-2-phenylindole JC-1, 5,5&prime ,6,6&prime -tetrachloro-1,1&prime ,3,3&prime -tetraethylbenzimidazolcarbocyanine iodide DTT, dithiothreitol ECL, enhanced chemiluminescence FBS, fetal bovine serum IAP, inhibitor of apoptosis protein MMP, mitochondrial membrane potential NAC, N-acetyl-l-cysteine pNA, p-nitroaniline PBS, phosphate-buffered saline PARP, poly (ADP-ribose) polymerase PI, propidium iodide ROS, reactive oxygen species |
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