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鉴定一种新型的IκBα激酶阻断剂,该阻断剂可通过抑制NF-κB调控的基因产物来增强细胞凋亡并抑制细胞侵袭。

Identification of a novel blocker of I kappa B alpha kinase that enhances cellular apoptosis and inhibits cellular invasion through suppression of NF-kappa B-regulated gene products.

作者信息

Ichikawa Haruyo, Takada Yasunari, Murakami Akira, Aggarwal Bharat B

机构信息

Cytokine Research Section, Department of Experimental Therapeutics, University of Texas M. D. Anderson Cancer Center, Houston, 77030, USA.

出版信息

J Immunol. 2005 Jun 1;174(11):7383-92. doi: 10.4049/jimmunol.174.11.7383.

Abstract

1'-Acetoxychavicol acetate (ACA), extracted from rhizomes of the commonly used ethno-medicinal plant Languas galanga, has been found to suppress chemical- and virus-induced tumor initiation and promotion through a poorly understood mechanism. Because several genes that regulate cellular proliferation, carcinogenesis, metastasis, and survival are regulated by activation of the transcription factor NF-kappaB, we postulated that ACA might mediate its activity through modulation of NF-kappaB activation. For this report, we investigated the effect of ACA on NF-kappaB and NF-kappaB-regulated gene expression activated by various carcinogens. We found that ACA suppressed NF-kappaB activation induced by a wide variety of inflammatory and carcinogenic agents, including TNF, IL-1beta, PMA, LPS, H(2)O(2), doxorubicin, and cigarette smoke condensate. Suppression was not cell type specific, because both inducible and constitutive NF-kappaB activations were blocked by ACA. ACA did not interfere with the binding of NF-kappaB to the DNA, but, rather, inhibited IkappaBalpha kinase activation, IkappaBalpha phosphorylation, IkappaBalpha degradation, p65 phosphorylation, and subsequent p65 nuclear translocation. ACA also inhibited NF-kappaB-dependent reporter gene expression activated by TNF, TNFR1, TNFR-associated death domain protein, TNFR-associated factor-2, and IkappaBalpha kinase, but not that activated by p65. Consequently, ACA suppressed the expression of TNF-induced NF-kappaB-regulated proliferative (e.g., cyclin D1 and c-Myc), antiapoptotic (survivin, inhibitor of apoptosis protein-1 (IAP1), IAP2, X-chromosome-linked IAP, Bcl-2, Bcl-x(L), Bfl-1/A1, and FLIP), and metastatic (cyclooxygenase-2, ICAM-1, vascular endothelial growth factor, and matrix metalloprotease-9) gene products. ACA also enhanced the apoptosis induced by TNF and chemotherapeutic agents and suppressed invasion. Overall, our results indicate that ACA inhibits activation of NF-kappaB and NF-kappaB-regulated gene expression, which may explain the ability of ACA to enhance apoptosis and inhibit invasion.

摘要

从常用民族药用植物高良姜的根茎中提取的乙酸1'-乙酰氧基查维醇(ACA),已被发现可通过一种尚未完全了解的机制抑制化学物质和病毒诱导的肿瘤起始和促进过程。由于几个调节细胞增殖、致癌作用、转移和存活的基因受转录因子NF-κB激活的调控,我们推测ACA可能通过调节NF-κB激活来介导其活性。在本报告中,我们研究了ACA对由各种致癌物激活的NF-κB以及NF-κB调控的基因表达的影响。我们发现ACA可抑制由多种炎症和致癌因子诱导的NF-κB激活,这些因子包括肿瘤坏死因子(TNF)、白细胞介素-1β(IL-1β)、佛波酯(PMA)、脂多糖(LPS)、过氧化氢(H₂O₂)、阿霉素和香烟烟雾浓缩物。抑制作用并非细胞类型特异性的,因为诱导型和组成型NF-κB激活均被ACA阻断。ACA并不干扰NF-κB与DNA的结合,而是抑制IκBα激酶激活、IκBα磷酸化、IκBα降解、p65磷酸化以及随后的p65核转位。ACA还抑制由TNF、肿瘤坏死因子受体1(TNFR1)、TNFR相关死亡结构域蛋白、TNFR相关因子-2(TRAF2)和IκBα激酶激活的NF-κB依赖性报告基因表达,但不抑制由p65激活的报告基因表达。因此,ACA抑制TNF诱导的NF-κB调控的增殖性(如细胞周期蛋白D1和c-Myc)、抗凋亡(存活素、凋亡抑制蛋白-1(IAP1)、IAP2、X染色体连锁IAP、Bcl-2、Bcl-xL、Bfl-1/A1和FLIP)以及转移性(环氧合酶-2、细胞间黏附分子-1、血管内皮生长因子和基质金属蛋白酶-9)基因产物的表达。ACA还增强了TNF和化疗药物诱导的细胞凋亡并抑制侵袭。总体而言,我们的结果表明ACA抑制NF-κB激活以及NF-κB调控的基因表达,这可能解释了ACA增强细胞凋亡和抑制侵袭的能力。

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