Targeting nuclear factor-κB activation pathway by thymoquinone:: Role in suppression of antiapoptotic gene products and enhancement of apoptosis (Publication with Expression of Concern. See vol. 16, pg. 1441, 2018)

被引:249
作者
Sethi, Gautam [1 ]
Ahn, Kwang Seok [1 ]
Aggarwal, Bharat B. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Cytokine Res Lab, Houston, TX 77030 USA
关键词
D O I
10.1158/1541-7786.MCR-07-2088
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Thymoquinone (TO), derived from the medicinal plant Nigella sativa, exhibits anti inflammatory and anticancer activities through mechanism(s) that is not fully understood. Because numerous effects modulated by TO can be linked to interference with the nuclear factor-kappa B (NF-kappa B) signaling, we investigated in detail the effect of this quinone on NF-kappa B pathway. As examined by DNA binding, we found that TO suppressed tumor necrosis factor-induced NF-kappa B activation in a dose- and time-dependent manner and inhibited NF-kappa B activation induced by various carcinogens and inflammatory stimuli. The suppression of NF-kappa B activation correlated with sequential inhibition of the activation of I kappa B alpha kinase, I kappa B alpha phosphorylation, I kappa B alpha degradation, p65 phosphorylation, p65 nuclear translocation, and the NF-kappa B-dependent reporter gene expression. TO specifically suppressed the direct binding of nuclear p65 and recombinant p65 to the DNA, and this binding was reversed by DTT. However, TO did not inhibit p65 binding to DNA when cells were transfected with the p65 plasmid containing cysteine residue 38 mutated to serine. TO also down-regulated the expression of NF-kappa B-regulated antiapoptotic (IAP1, IAP2, XIAP Bcl-2, Bcl-xL, and survivin), proliferative (cyclin D1, cyclooxygenase-2, and c-Myc), and angiogenic (matrix metalloproteinase-9 and vascular endothelial growth factor) gene products. This led to potentiation of apoptosis induced by tumor necrosis factor and chemotherapeutic agents. Overall, our results indicate that the anticancer and anti inflammatory activities previously assigned to TO may be mediated in part through the suppression of the NF-kappa B activation pathway, as shown here, and thus may have potential in treatment of myeloid leukemia and other cancers.
引用
收藏
页码:1059 / 1070
页数:12
相关论文
共 73 条
[51]   Plumbagin (5-hydroxy-2-methyl-1,4-naphthoquinone) suppresses NF-κB activation and NF-κB-regulated gene products through modulation of p65 and IκBα kinase activation, leading to potentiation of apoptosis induced by cytokine and chemotherapeutic agents [J].
Sandur, Santosh K. ;
Ichikawa, Haruyo ;
Sethi, Gautam ;
Ahn, Kwang Seok ;
Aggarwal, Bharat B. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (25) :17023-17033
[52]   Thymoquinone decreases AGE induced NF-κB activation in proximal tubular eplithelial cells [J].
Sayed, Ahmed Amir Radwan ;
Morcos, Michael .
PHYTOTHERAPY RESEARCH, 2007, 21 (09) :898-899
[53]   INDUCIBILITY OF KAPPA-IMMUNOGLOBULIN ENHANCER-BINDING PROTEIN NF-KAPPA-B BY A POSTTRANSLATIONAL MECHANISM [J].
SEN, R ;
BALTIMORE, D .
CELL, 1986, 47 (06) :921-928
[54]   Celastrol, a novel triterpene, potentiates TNF-induced apoptosis and suppresses invasion of tumor cells by inhibiting NF-κB-regulated gene products and TAK1-mediated NF-κB activation [J].
Sethi, Gautam ;
SeokAhn, Kwang ;
Pandey, Manoj K. ;
Aggarwal, Bharat B. .
BLOOD, 2007, 109 (07) :2727-2735
[55]   Indirubin enhances tumor necrosis factor-induced apoptosis through modulation of nuclear factor-κB signaling pathway [J].
Sethi, Gautam ;
Ahn, Kwang Seok ;
Sandur, Santosh K. ;
Lin, Xin ;
Chaturvedi, Madan M. ;
Aggarwal, Bharat B. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (33) :23425-23435
[56]   Inhibition of NF-κB activity decreases the VEGF mRNA expression in MDA-MB-231 breast cancer cells [J].
Shibata, A ;
Nagaya, T ;
Imai, T ;
Funahashi, H ;
Nakao, A ;
Seo, H .
BREAST CANCER RESEARCH AND TREATMENT, 2002, 73 (03) :237-243
[57]  
Shishodia Shishir, 2004, Cancer Treat Res, V119, P139
[58]  
Shoieb AM, 2003, INT J ONCOL, V22, P107
[59]   Mechanisms by which IκB proteins control NF-κB activity [J].
Simeonidis, S ;
Stauber, D ;
Chen, GY ;
Hendrickson, WA ;
Thanos, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (01) :49-54
[60]   Nuclear factor (NF)-κB-regulated X-chromosome-linked iap gene expression protects endothelial cells from tumor necrosis factor α-induced apoptosis [J].
Stehlik, C ;
de Martin, R ;
Kumabashiri, I ;
Schmid, JA ;
Binder, BR ;
Lipp, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (01) :211-216