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姜黄素通过非依赖CHOP的DR5上调使肿瘤坏死因子相关凋亡诱导配体(TRAIL)介导的凋亡敏感化。

Curcumin sensitizes tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-mediated apoptosis through CHOP-independent DR5 upregulation.

作者信息

Jung Eun Mi, Park Jong-Wook, Choi Kyeong Sook, Park Jeen-Woo, Lee Hyung Il, Lee Kyung-Seop, Kwon Taeg Kyu

机构信息

Department of Immunology, School of Medicine, Keimyung University, Taegu 700-712, South Korea.

出版信息

Carcinogenesis. 2006 Oct;27(10):2008-17. doi: 10.1093/carcin/bgl026. Epub 2006 Apr 12.

Abstract

Death receptor DR5 (DR5/TRAIL-R2) is an apoptosis-inducing membrane receptor for tumor necrosis factor-related apoptosis-inducing ligand (TRAIL). In this study, we showed that curcumin, a plant product containing the phenolic phytochemical, is a potent enhancer of TRAIL-induced apoptosis through upregulation of DR5 expression. Both treatment with DR5/Fc chimeric protein and silencing of DR5 expression using small interfering RNA (siRNA) attenuated curcumin plus TRAIL-induced apoptosis, showing that the critical role of DR5 in this cell death. Curcumin also induced the expression of a potential pro-apoptotic gene, C/EBP homologous protein (CHOP), both at its mRNA and protein levels. However, suppression of CHOP expression by small interfering RNA did not abrogate the curcumin-mediated induction of DR5 and the cell death induced by curcumin plus TRAIL, demonstrating that CHOP is not involved in curcumin-induced DR5 upregulation. Taken together, the present study demonstrates that curcumin enhances TRAIL-induced apoptosis by CHOP-independent upregulation of DR5.

摘要

死亡受体DR5(DR5/TRAIL-R2)是肿瘤坏死因子相关凋亡诱导配体(TRAIL)的一种诱导凋亡的膜受体。在本研究中,我们表明姜黄素,一种含有酚类植物化学物质的植物产物,通过上调DR5表达是TRAIL诱导凋亡的有效增强剂。用DR5/Fc嵌合蛋白处理和使用小干扰RNA(siRNA)沉默DR5表达均减弱了姜黄素加TRAIL诱导的凋亡,表明DR5在这种细胞死亡中起关键作用。姜黄素还在其mRNA和蛋白质水平上诱导了一种潜在的促凋亡基因C/EBP同源蛋白(CHOP)的表达。然而,小干扰RNA抑制CHOP表达并未消除姜黄素介导的DR5诱导以及姜黄素加TRAIL诱导的细胞死亡,表明CHOP不参与姜黄素诱导的DR5上调。综上所述,本研究表明姜黄素通过不依赖CHOP的DR5上调增强TRAIL诱导的凋亡。

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