Modulation of anti-apoptotic and survival pathways by curcumin as a strategy to induce apoptosis in cancer cells

被引:314
作者
Reuter, Simone [1 ]
Eifes, Serge [1 ]
Dicato, Mario [1 ]
Aggarwal, Bharat B. [2 ]
Diederich, Marc [1 ]
机构
[1] Hop Kirchberg, Lab Biol Mol & Cellulaire Canc, L-2540 Luxembourg, Luxembourg
[2] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Cytokine Res Lab, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Curcumin; Apoptosis; Cancer; Cell signaling pathways; Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL);
D O I
10.1016/j.bcp.2008.07.031
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Apoptosis is a highly regulated mechanism by which cells undergo cell death in an active way. As one of the most challenging tasks concerning cancer is to induce apoptosis in malignant cells, researchers increasingly focus on natural products to modulate apoptotic signaling pathways. Curcumin, a natural compound isolated from the plant Curcuma longa, has chemopreventive properties, which are mainly due to its ability to arrest cell cycle and to induce apoptosis. This article reviews the main effects of curcumin on the different apoptotic signaling pathways involved in curcumin-induced apoptosis of cancer cells, including the intrinsic and extrinsic apoptosis pathways, the NF-kappa B-mediated pathway as well as the PI3K/Akt signaling pathway. This review also focuses on the sensitization of cells to TRAIL-induced apoptosis after curcumin treatment and shows that curcumin enhances the capacity to induce cell death of different chemotherapeutical drugs. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1340 / 1351
页数:12
相关论文
共 128 条
[1]   Curcumin suppresses the paclitaxel-induced nuclear factor-κB pathway in breast cancer cells and inhibits lung metastasis of human breast cancer in nude mice [J].
Aggarwal, BB ;
Shishodia, S ;
Takada, Y ;
Banerjee, S ;
Newman, RA ;
Bueso-Ramos, CE ;
Price, JE .
CLINICAL CANCER RESEARCH, 2005, 11 (20) :7490-7498
[2]   Inhibition of growth and survival of human head and neck squamous cell carcinoma cells by curcumin via modulation of nuclear factor-κB signaling [J].
Aggarwal, S ;
Takada, Y ;
Singh, S ;
Myers, JN ;
Aggarwal, BB .
INTERNATIONAL JOURNAL OF CANCER, 2004, 111 (05) :679-692
[3]   Curcumin (diferuloylmethane) induces apoptosis through activation of caspase-8, BID cleavage and cytochrome c release: its suppression by ectopic expression of Bcl-2 and Bcl-xl [J].
Anto, RJ ;
Mukhopadhyay, A ;
Denning, K ;
Aggarwal, BB .
CARCINOGENESIS, 2002, 23 (01) :143-150
[4]   Evidence that curcumin suppresses the growth of malignant gliomas in vitro and in vivo through induction of autophagy: Role of Akt and extracellular signal-regulated kinase signaling pathways [J].
Aoki, Hiroshi ;
Takada, Yasunari ;
Kondo, Seiji ;
Sawaya, Raymond ;
Aggarwal, Bharat B. ;
Kondo, Yasuko .
MOLECULAR PHARMACOLOGY, 2007, 72 (01) :29-39
[5]   Targeting death and decoy receptors of the tumour-necrosis factor superfamily [J].
Ashkenazi, A .
NATURE REVIEWS CANCER, 2002, 2 (06) :420-430
[6]   Induction of early apoptosis and ROS-generation activity in human gingival fibroblasts (HGF) and human submandibular gland carcinoma (HSG) cells treated with curcumin [J].
Atsumi, Toshiko ;
Tonosaki, Keiichi ;
Fujisawa, Seiichiro .
ARCHIVES OF ORAL BIOLOGY, 2006, 51 (10) :913-921
[7]   Ruthenium red, inhibitor of mitochondrial Ca2+ uniporter, inhibits curcumin-induced apoptosis via the prevention of intracellular Ca2+ depletion and cytochrome c release [J].
Bae, JH ;
Park, JW ;
Kwon, TK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 303 (04) :1073-1079
[8]  
BAKHSHI W, 2008, COUPLING ENDOPLASMIC, V13, P904
[9]   Control of apoptosis by Rel/NF-κB transcription factors [J].
Barkett, M ;
Gilmore, TD .
ONCOGENE, 1999, 18 (49) :6910-6924
[10]   Sensitization of taxol-induced apoptosis by curcumin involves down-regulation of nuclear factor-κB and the serine/threonine kinase Akt and is independent of tubulin polymerization [J].
Bava, SV ;
Puliappadamba, VT ;
Deepti, A ;
Nair, A ;
Karunagaran, D ;
Anto, RJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (08) :6301-6308