Restoration of ASC expression sensitizes colorectal cancer cells to genotoxic stress-induced caspase-independent cell death

被引:19
作者
Hong, Sujeong [1 ,2 ,3 ]
Hwang, Inhwa [1 ,2 ]
Lee, Yun-Sun [4 ]
Park, Sangjun [1 ,2 ]
Lee, Won-Keun [3 ]
Fernandes-Alnemri, Teresa
Alnemri, Emad S. [5 ]
Kim, You-Sun [4 ]
Yu, Je-Wook [1 ,2 ]
机构
[1] Yonsei Univ, Coll Med, Dept Microbiol, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Brain Korea Project Med Sci 21, Seoul, South Korea
[3] Myongji Univ, Div Biosci & Bioinformat, Yongin, South Korea
[4] Ajou Univ, Sch Med, Inst Med Sci, Suwon 441749, South Korea
[5] Thomas Jefferson Univ, Kimmel Canc Ctr, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
关键词
ASC; DLD-1; Methylation; DNA damaging agent; Cell death; RECRUITMENT DOMAIN PROTEIN; NLRP3; INFLAMMASOME; ACTIVATING ADAPTER; EPIGENETIC INACTIVATION; APOPTOSIS; METHYLATION; GENE; ASC/TMS1; NECROSIS; DNA;
D O I
10.1016/j.canlet.2012.12.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC), an essential component of the inflammasome complex, is frequently silenced by epigenetic methylation in many tumor cells. Here, we demonstrate that restoration of ASC expression in human colorectal cancer DLD-1 cells, in which ASC is silenced by aberrant methylation, potentiated cell death mediated by DNA damaging agent. Contrarily, ASC knockdown in HT-29 cells rendered cells less susceptible to etoposide toxicity. The increased susceptibility of ASC-expressing DLD-1 cells to genotoxic stress was independent of inflammasome or caspase activation, but partially dependent on mitochondrial ROS production and JNK activation. Thus, our data suggest that ASC expression in cancer cells is an important factor in determining their susceptibility to chemotherapy. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:183 / 191
页数:9
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