Withaferin A enhances radiation-induced apoptosis in Caki cells through induction of reactive oxygen species, BcI-2 downregulation and Akt inhibition

被引:57
作者
Yang, Eun Sun [1 ]
Choi, Min Jung [1 ]
Kim, Jin Hee [2 ]
Choi, Kyeong Sook [3 ]
Kwon, Taeg Kyu [1 ]
机构
[1] Keimyung Univ, Sch Med, Dept Immunol, Taegu 704701, South Korea
[2] Keimyung Univ, Sch Med, Dept Radiat Oncol, Taegu 704701, South Korea
[3] Ajou Univ, Sch Med, Inst Med Sci, Dept Mol Sci & Technol, Suwon 442749, South Korea
关键词
Withaferin A; Radiation; Apoptosis; Reactive oxygen species; BcI-2; NF-KAPPA-B; COMPOUND WITHAFERIN; CANCER CELLS; DEATH; RADIOSENSITIVITY; GENERATION; ROS; ACTIVATION; PROTEASOME; PATHWAYS;
D O I
10.1016/j.cbi.2011.01.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Withaferin A (Wit A), a natural compound derived from the medicinal plant Withania somnifera, has been reported for the anti-tumor effects, including the inhibition of tumor cell growth, metastasis and angiogenesis. In this study, we investigated the effect of Wit A on radiation-induced apoptosis in human renal cancer cells (Caki cells). Our results showed that, compared with Wit A or radiation alone, the combination of both resulted in a significant enhancement of apoptosis, showing the increase in the cleavage of caspase-3 and PARP as well as sub-G1 cell population. In addition, reactive oxygen species (ROS) generation was correlated with the enhancement of radiation-induced apoptosis by Wit A. Wit A downregulated BcI-2 protein levels and ectopic expression of BcI-2 in Caki cells attenuated the apoptosis induced by Wit A plus radiation. Taken together, these results indicate that Wit A enhanced radiation-induced apoptosis in Caki cells through ROS generation, down-regulation of BcI-2 and Akt dephosphorylation. Thus, our study shows that Wit A may be used as an effective radiosensitizer in cancer therapy. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 15
页数:7
相关论文
共 34 条
[1]   Generation of superoxide anion by equine spermatozoa as detected by dihydroethidium [J].
Burnaugh, L. ;
Sabeur, K. ;
Ball, B. A. .
THERIOGENOLOGY, 2007, 67 (03) :580-589
[2]   INTEGRINS AND SIGNAL-TRANSDUCTION PATHWAYS - THE ROAD TAKEN [J].
CLARK, EA ;
BRUGGE, JS .
SCIENCE, 1995, 268 (5208) :233-239
[3]   Cellular survival: a play in three Akts [J].
Datta, SR ;
Brunet, A ;
Greenberg, ME .
GENES & DEVELOPMENT, 1999, 13 (22) :2905-2927
[4]   Akt phosphorylation of BAD couples survival signals to the cell-intrinsic death machinery [J].
Datta, SR ;
Dudek, H ;
Tao, X ;
Masters, S ;
Fu, HA ;
Gotoh, Y ;
Greenberg, ME .
CELL, 1997, 91 (02) :231-241
[5]   Caspase inhibitors [J].
Ekert, PG ;
Silke, J ;
Vaux, DL .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (11) :1081-1086
[6]   Cytosolic and mitochondrial ROS in staurosporine-induced retinal cell apoptosis [J].
Gil, J ;
Almeida, S ;
Oliveira, CR ;
Rego, AC .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (11) :1500-1514
[7]  
GOU HR, 2006, INT J RADIAT BIOL, V82, P97
[8]   The Combination of Berberine and Irradiation Enhances Anti-Cancer Effects Via Activation of p38 MAPK Pathway and ROS Generation in Human Hepatoma Cells [J].
Hur, Jung-Mu ;
Hyun, Mee-Sun ;
Lim, Sang-Yong ;
Lee, Woo-Yiel ;
Kim, Dongho .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 107 (05) :955-964
[9]   The chemopreventive agent curcumin is a potent radiosensitizer of human cervical tumor cells via increased reactive oxygen species production and overactivation of the mitogen-activated protein kinase pathway [J].
Javvadi, Prashanthi ;
Segan, Andrew T. ;
Tuttle, Stephen W. ;
Koumenis, Constantinos .
MOLECULAR PHARMACOLOGY, 2008, 73 (05) :1491-1501
[10]   Cancer statistics, 2006 [J].
Jemal, A ;
Siegel, R ;
Ward, E ;
Murray, T ;
Xu, JQ ;
Smigal, C ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2006, 56 (02) :106-130