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合成异硫氰酸酯的抗核因子-κB及抗炎活性:化学结构与细胞信号传导的作用

Anti-NF-kappaB and anti-inflammatory activities of synthetic isothiocyanates: effect of chemical structures and cellular signaling.

作者信息

Prawan Auemduan, Saw Constance Lay Lay, Khor Tin Oo, Keum Young-Sam, Yu Siwang, Hu Longqin, Kong Ah-Ng

机构信息

Center for Cancer Prevention Research, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, United States.

出版信息

Chem Biol Interact. 2009 May 15;179(2-3):202-11. doi: 10.1016/j.cbi.2008.12.014. Epub 2008 Dec 30.

Abstract

Many cancer chemopreventive agents have been associated with lower cancer risk by suppressing nuclear factor-kappaB (NF-kappaB) signaling pathways, which subsequently leads to attenuated pro-inflammatory mediators and activities. Of the natural compounds, the isothiocyanates (ITCs) found in cruciferous vegetables have received particular attention because of their potential anti-cancer effects. However, limited studies regarding the influence of ITCs structure on NF-kappaB transactivation and anti-inflammatory action are reported. In the present study, the anti-inflammatory potential of ten structurally divergent synthetic ITCs were evaluated in HT-29-N9 human colon cancer cells and RAW 264.7 murine macrophages. The effect of ITCs on the basal transcriptional activation of NF-kappaB and the inflammatory response to bacterial lipopolysaccharide (LPS) were assessed. The synthetic ITC analogs suppressed NF-kappaB-mediated pro-inflammatory gene transcription. Among the ITC analogs, tetrahydrofurfuryl isothiocyanate, methyl-3-isothiocyanatopropionate, 3-morpholinopropyl isothiocyanate and 3,4-methyelendioxybenzyl isothiocyanate showed stronger NF-kappaB inhibition as compared to the parent compound, phenylethyl isothiocyanate (PEITC). Molecular analysis revealed that several of the pro-inflammatory mediators and cytokines (iNOS, COX-2, IL-1beta, IL-6 and TNF-alpha) were reduced by ITCs, and correlated with the downregulation of NF-kappaB signaling pathways. Immunoblotting showed that ITCs suppressed LPS-induced phosphorylation and degradation of IkappaB alpha and decreased nuclear translocation of p65. In parallel, ITCs suppressed the phosphorylation of IkappaB kinase alpha/beta (IKKalpha/beta). Taken together, our findings provide the possibility that synthetic ITC analogs might have promising cancer chemopreventive potential, based on their stronger anti-NF-kappaB and anti-inflammatory activities, than the natural ITCs.

摘要

许多癌症化学预防剂通过抑制核因子-κB(NF-κB)信号通路与降低癌症风险相关,这随后导致促炎介质和活性减弱。在天然化合物中,十字花科蔬菜中发现的异硫氰酸酯(ITC)因其潜在的抗癌作用而受到特别关注。然而,关于ITC结构对NF-κB反式激活和抗炎作用影响的研究报道有限。在本研究中,在HT-29-N9人结肠癌细胞和RAW 264.7小鼠巨噬细胞中评估了十种结构不同的合成ITC的抗炎潜力。评估了ITC对NF-κB基础转录激活的影响以及对细菌脂多糖(LPS)的炎症反应。合成ITC类似物抑制NF-κB介导的促炎基因转录。在ITC类似物中,与母体化合物苯乙基异硫氰酸酯(PEITC)相比,四氢糠基异硫氰酸酯、3-异硫氰酸基丙酸甲酯、3-吗啉基丙基异硫氰酸酯和3,4-亚甲二氧基苄基异硫氰酸酯显示出更强的NF-κB抑制作用。分子分析表明,几种促炎介质和细胞因子(诱导型一氧化氮合酶、环氧化酶-2、白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α)被ITC降低,并与NF-κB信号通路的下调相关。免疫印迹显示,ITC抑制LPS诱导的IκBα磷酸化和降解,并减少p65的核转位。同时,ITC抑制IκB激酶α/β(IKKα/β)的磷酸化。综上所述,我们的研究结果表明,基于其比天然ITC更强的抗NF-κB和抗炎活性,合成ITC类似物可能具有有前景的癌症化学预防潜力。

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