Caspase-dependent cleavage of BAG3 in proteasome inhibitors-induced apoptosis in thyroid cancer cells

被引:34
|
作者
Du, Zhen-Xian [2 ]
Meng, Xin [1 ]
Zhang, Hai-Yan [3 ]
Guan, Yifu [1 ]
Wang, Hua-Qin [1 ]
机构
[1] China Med Univ, Dept Biochem & Mol Biol, Shenyang 110001, Peoples R China
[2] China Med Univ, Affiliated Hosp 1, Dept Endocrinol & Metab, Shenyang 110001, Peoples R China
[3] China Med Univ, Affiliated Hosp 1, Dept Geriatr, Shenyang 110001, Peoples R China
基金
中国国家自然科学基金;
关键词
BAG3; caspase; apoptosis; cleavage;
D O I
10.1016/j.bbrc.2008.02.112
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
Proteasome inhibitors are emerging as effective drugs for the treatment of relapsed/refractory multiple myeloma and possibly some solid tumors. Bcl-2-associated athanogene 3 (BAG3) is a survival protein that has been shown to be stimulated during cell response to stressful conditions, such as exposure to high temperature, heavy metals. We have recently demonstrated that BAG3 is also induced by proteasome inhibitors at the transcriptional level and the induction of BAG3 by proteasome inhibition is antiapoptotic. Here, we demonstrated that although proteasome inhibitors triggered similar upregulation of BAG3 transcript in sensitive and insensitive thyroid cancer cells, persistent increase of BAG3 protein was detected in insensitive cells, whereas less increase or even decrease was observed in sensitive cells. Notably, decrease of BAG3 protein was associated with the appearance of a BAG3 fragment of approximately 40 kDa, which appeared to be caspase-dependent. Therefore, caspase-dependent cleavage of BAG3 might facilitate apoptosis in sensitive cells. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:894 / 898
页数:5
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