Reversal of chemoresistance and enhancement of apoptosis by statins through down-regulation of the NF-κB pathway

被引:97
|
作者
Ahn, Kwang Seok [1 ]
Sethi, Gautam [1 ]
Aggarwal, Bharat B. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Citokine Res Lab, Unit 143, Houston, TX 77030 USA
关键词
simvastatin; nuclear factor-kappaB; chemotherapeutic agents; apoptosis; TRANSCRIPTION FACTOR; GENE-PRODUCTS; CANCER CELLS; RISK; ACTIVATION; REDUCTASE; THERAPY; DRUGS;
D O I
10.1016/j.bcp.2007.10.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We recently found that simvastatin can modulate the nuclear factor-kappa B (NF-kappa B) activation pathway, but whether other statins have similar effects to those of simvastatin is unknown. Therefore, we evaluated the effect six different statins on TNF-induced NF-kappa B activation in human myeloid leukemia cells. We then determined whether the combination of statins and standard chemotherapeutic agents could overcome chemoresistance and augment apoptosis. Of the six statins evaluated, only the natural statins (simvastatin, mevastatin, lovastatin, and pravastatin), not the synthetic statins (fluvastatin and atorvastatin), inhibited TNF-induced NF-kappa B activation. Simvastatin suppressed the NF-kappa B activation and potentiated the apoptosis induced by doxorubicin, paclitaxel, and 5-fluorouracil. These results suggest that different statins behave differently from one another and that they may be useful in overcoming chemoresistance. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:907 / 913
页数:7
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