A Fas-associated Death Domain Protein-dependent mechanism mediates the apoptotic action of non-steroidal anti-inflammatory drugs in the human leukemic Jurkat cell line

被引:39
|
作者
Han, ZY
Pantazis, P
Wyche, JH
Kouttab, N
Kidd, VJ
Hendrickson, EA
机构
[1] Univ Minnesota, Sch Med, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[2] Brown Univ, Dept Mol Biol Cell Biol & Biochem, Providence, RI 02912 USA
[3] Boston Univ, Dept Pathol, Roger Williams Med Ctr, Providence, RI 02906 USA
[4] St Jude Childrens Res Hosp, Dept Tumor Cell Biol, Memphis, TN 38101 USA
[5] Univ Minnesota, Sch Med, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
关键词
D O I
10.1074/jbc.M106214200
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
Non-steroidal anti-inflammatory drugs (NSAIDs) are inhibitors of cyclooxygenase-1 and -2 and are useful for prevention and cure of cancers, especially colon and rectal cancers. The NSAIDs indomethacin and sulindac sulfide have been shown to induce apoptosis of colon epithelial cancer cells by a Bax-dependent mechanism that involves mitochondria-mediated activation of a caspase-9-dependent pathway. In this report, we demonstrate that indomethacin and sulindac sulfide induce apoptosis of human leukemic Jurkat cells by a mechanism that requires the Fas-associated Death Domain Protein-mediated activation of a caspase-8-dependent pathway. Therefore, NSAIDs induce apoptosis by different mechanisms depending on the cell type.
引用
收藏
页码:38748 / 38754
页数:7
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