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乙酰-11-酮基-β-乳香酸通过抑制核因子κB(NF-κB)及其调控的基因表达来增强细胞凋亡、抑制侵袭并消除破骨细胞生成。

Acetyl-11-keto-beta-boswellic acid potentiates apoptosis, inhibits invasion, and abolishes osteoclastogenesis by suppressing NF-kappa B and NF-kappa B-regulated gene expression.

作者信息

Takada Yasunari, Ichikawa Haruyo, Badmaev Vladimir, Aggarwal Bharat B

机构信息

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

出版信息

J Immunol. 2006 Mar 1;176(5):3127-40. doi: 10.4049/jimmunol.176.5.3127.

Abstract

Acetyl-11-keto-beta-boswellic acid (AKBA), a component of an Ayurvedic therapeutic plant Boswellia serrata, is a pentacyclic terpenoid active against a large number of inflammatory diseases, including cancer, arthritis, chronic colitis, ulcerative colitis, Crohn's disease, and bronchial asthma, but the mechanism is poorly understood. We found that AKBA potentiated the apoptosis induced by TNF and chemotherapeutic agents, suppressed TNF-induced invasion, and inhibited receptor activator of NF-kappaB ligand-induced osteoclastogenesis, all of which are known to require NF-kappaB activation. These observations corresponded with the down-regulation of the expression of NF-kappaB-regulated antiapoptotic, proliferative, and angiogenic gene products. As examined by DNA binding, AKBA suppressed both inducible and constitutive NF-kappaB activation in tumor cells. It also abrogated NF-kappaB activation induced by TNF, IL-1beta, okadaic acid, doxorubicin, LPS, H2O2, PMA, and cigarette smoke. AKBA did not directly affect the binding of NF-kappaB to the DNA but inhibited sequentially the TNF-induced activation of IkappaBalpha kinase (IKK), IkappaBalpha phosphorylation, IkappaBalpha ubiquitination, IkappaBalpha degradation, p65 phosphorylation, and p65 nuclear translocation. AKBA also did not directly modulate IKK activity but suppressed the activation of IKK through inhibition of Akt. Furthermore, AKBA inhibited the NF-kappaB-dependent reporter gene expression activated by TNFR type 1, TNFR-associated death domain protein, TNFR-associated factor 2, NF-kappaB-inducing kinase, and IKK, but not that activated by the p65 subunit of NF-kappaB. Overall, our results indicated that AKBA enhances apoptosis induced by cytokines and chemotherapeutic agents, inhibits invasion, and suppresses osteoclastogenesis through inhibition of NF-kappaB-regulated gene expression.

摘要

乙酰-11-酮基-β-乳香酸(AKBA)是阿育吠陀治疗植物锯叶乳香中的一种成分,是一种五环萜类化合物,对包括癌症、关节炎、慢性结肠炎、溃疡性结肠炎、克罗恩病和支气管哮喘在内的多种炎症性疾病具有活性,但作用机制尚不清楚。我们发现,AKBA可增强TNF和化疗药物诱导的细胞凋亡,抑制TNF诱导的侵袭,并抑制核因子κB受体激活剂配体诱导的破骨细胞生成,所有这些都已知需要核因子κB激活。这些观察结果与核因子κB调节的抗凋亡、增殖和血管生成基因产物表达的下调一致。通过DNA结合检测,AKBA可抑制肿瘤细胞中诱导型和组成型核因子κB的激活。它还可消除TNF、IL-1β、冈田酸、阿霉素、LPS、H2O2、PMA和香烟烟雾诱导的核因子κB激活。AKBA不会直接影响核因子κB与DNA的结合,但会依次抑制TNF诱导的IκBα激酶(IKK)激活、IκBα磷酸化、IκBα泛素化、IκBα降解、p65磷酸化和p65核转位。AKBA也不会直接调节IKK活性,但通过抑制Akt来抑制IKK的激活。此外,AKBA可抑制由1型肿瘤坏死因子受体、肿瘤坏死因子受体相关死亡结构域蛋白、肿瘤坏死因子受体相关因子2、核因子κB诱导激酶和IKK激活的核因子κB依赖性报告基因表达,但不会抑制由核因子κB的p65亚基激活的报告基因表达。总体而言,我们的结果表明,AKBA通过抑制核因子κB调节的基因表达来增强细胞因子和化疗药物诱导的细胞凋亡,抑制侵袭,并抑制破骨细胞生成。

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