The XIAP inhibitor Embelin enhances TRAIL-mediated apoptosis in malignant glioma cells by down-regulation of the short isoform of FLIP

被引:53
作者
Siegelin, M. D. [1 ,2 ]
Gaiser, Timo [2 ]
Siegelin, Y. [3 ]
机构
[1] Univ Massachusetts, Dept Canc Biol, Sch Med, Worcester, MA 01605 USA
[2] Univ Heidelberg Hosp, Dept Neuropathol, D-69120 Heidelberg, Germany
[3] Goethe Univ Frankfurt, Poliklin Parodontol, Zentrum Zahn Mund & Kieferheilkunde Carolinum, D-60590 Frankfurt, Germany
关键词
Glioma; TRAIL/Apo2L; c-FLIP; Embelin; DR5; UP-REGULATION; PROTEASOMAL DEGRADATION; SIGNALING COMPLEX; C-FLIP; DEATH; LIGAND; CELECOXIB; PATHWAY; PROTEIN;
D O I
10.1016/j.neuint.2009.04.011
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
Embelin has been reported to exhibit therapeutic activity in cancer. In this study glioblastoma cells and human astrocytes were treated with Embelin, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) or the combination of both. Treatment with subtoxic doses of Embelin broadly sensitized malignant glioma cells to TRAIL-mediated apoptosis. Notably, human astrocytes were not significantly affected by the combined treatment consisting of Embelin and TRAIL Combined treatment with Embelin and TRAIL augmented the activation of initiator caspases-8/-9 and effector caspases-3/-7, respectively. Furthermore, Embelin down-regulated the expression of the long- and short-isoform of c-FLIP. In addition, forced expression of the short isoform of c-FLIP (S) attenuated apoptosis induced by the combination of Embelin and TRAIL. Embelin did not modulate the mRNA levels of c-FLIP (S), suggesting that Embelin modulates the expression of c-FLIP in a posttranscriptional manner. In summary, the short isoform of c-FLIP is a key regulator in TRAIL-Embelin-mediated apoptosis in malignant glioma. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:423 / 430
页数:8
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