Amorfrutin A inhibits TNF-α-induced NF-κB activation and NF-κB-regulated target gene products

被引:30
作者
Shi, Hui [2 ]
Ma, Juan [1 ,2 ]
Mi, Chunliu [2 ,3 ]
Li, Jing [2 ,3 ]
Wang, Fei [1 ,2 ]
Lee, Jung Joon [2 ]
Jin, Xuejun [1 ,2 ]
机构
[1] Yanbian Univ, Coll Pharm, Minist Educ, Key Lab Nat Resources Changbai Mt & Funct Mol, Yanji 133002, Jilin Province, Peoples R China
[2] Yanbian Univ, Mol Canc Res Ctr, Yanji 133002, Jilin Province, Peoples R China
[3] Yanbian Univ, Dept Chem, Minist Educ, Key Lab Nat Resources Changbai Mt & Funct Mol, Yanji 133002, Jilin Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Amorfrutin A; Nuclear factor-kappa B (NF-kappa B); I kappa B alpha; Inflammation; Apoptosis; INSULIN-RESISTANCE; IKK-BETA; INFLAMMATION; CANCER; UBIQUITINATION; KINASE; PATHWAYS; IMMUNITY; COMPLEX;
D O I
10.1016/j.intimp.2014.04.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The nuclear factor-kappa B (NF-kappa B) transcription factors control many physiological processes including inflammation, immunity, apoptosis, and angiogenesis. In our search for NF-kappa B inhibitors from natural resources, we identified amorfrutin A as an inhibitor of NF-kappa B activation from the fruits of Amorpha fruticosa L. In present study, this compound significantly inhibited the TNF-alpha-induced expression of NF-kappa B reporter gene. Further analysis revealed that amorfrutin A was a potent inhibitor of NF-kappa B activation by the suppression of TNF-alpha-induced inhibitor of kappa B alpha (I kappa B alpha) degradation, p65 nuclear translocation, and DNA-binding activity of NF-kappa B. We also demonstrated that pretreatment of cells with this compound prevented the TNF-alpha-induced expression of NF-kappa B target genes, such as antiapoptosis (cIAP-1 and FLIP), proliferation (COX-2 and cyclinD1), invasion (MMP-9), angiogenesis (VEGF), and major inflammatory cytokines (TNF-alpha, IL-8, and MCP1). Furthermore, our results suggest that amorfrutin A potentiates TNF-alpha-induced apoptosis. Taken together, amorfrutin A could be a valuable candidate for the intervention of NF-kappa B-dependent pathological conditions such as inflammation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:56 / 62
页数:7
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