Department of Psychiatry and Behavioral Sciences, Emory University, 1365-B Clifton Road, Atlanta, GA 30322, USA.
Int Immunopharmacol. 2012 Feb;12(2):368-77. doi: 10.1016/j.intimp.2011.12.009. Epub 2011 Dec 22.
Nuclear factor kappa B (NF-κB) is a key signaling molecule in the elaboration of the inflammatory response. Data indicate that curcumin, a natural ingredient of the curry spice turmeric, acts as a NF-κB inhibitor and exhibits both anti-inflammatory and anti-cancer properties. Curcumin analogs with enhanced activity on NF-κB and other inflammatory signaling pathways have been developed including the synthetic monoketone compound 3,5-Bis(2-fluorobenzylidene)-4-piperidone (EF24). 3,5-Bis(2-pyridinylmethylidene)-4-piperidone (EF31) is a structurally-related curcumin analog whose potency for NF-κB inhibition has yet to be determined. To examine the activity of EF31 compared to EF24 and curcumin, mouse RAW264.7 macrophages were treated with EF31, EF24, curcumin (1-100 μM) or vehicle (DMSO 1%) for 1h. NF-κB pathway activity was assessed following treatment with lipopolysaccharide (LPS) (1 μg/mL). EF31 (IC(50)5 μM) exhibited significantly more potent inhibition of LPS-induced NF-κB DNA binding compared to both EF24 (IC(50)35 μM) and curcumin (IC(50) >50 μM). In addition, EF31 exhibited greater inhibition of NF-κB nuclear translocation as well as the induction of downstream inflammatory mediators including pro-inflammatory cytokine mRNA and protein (tumor necrosis factor-α, interleukin-1β, and interleukin-6). Regarding the mechanism of these effects on NF-κB, EF31 (IC(50)1.92 μM) exhibited significantly greater inhibition of IκB kinase β compared to EF24 (IC(50)131 μM). Finally, EF31 demonstrated potent toxicity in NF-κB-dependent cancer cell lines while having minimal and reversible toxicity in RAW264.7 macrophages. These data indicate that EF31 is a more potent inhibitor of NF-κB activity than either EF24 or curcumin while exhibiting both anti-inflammatory and anticancer activities. Thus, EF31 represents a promising curcumin analog for further therapeutic development.
核因子 kappa B(NF-κB)是炎症反应的关键信号分子。有数据表明,姜黄素是咖喱香料姜黄中的一种天然成分,作为 NF-κB 抑制剂,具有抗炎和抗癌特性。已经开发出了对 NF-κB 和其他炎症信号通路具有增强活性的姜黄素类似物,包括合成的单酮化合物 3,5-双(2-氟苯亚甲基)-4-哌啶酮(EF24)。3,5-双(2-吡啶基亚甲基)-4-哌啶酮(EF31)是一种结构相关的姜黄素类似物,其 NF-κB 抑制作用的效力尚未确定。为了研究 EF31 与 EF24 和姜黄素的活性,用 EF31、EF24、姜黄素(1-100 μM)或载体(DMSO1%)处理 RAW264.7 巨噬细胞 1 小时。用脂多糖(LPS)(1 μg/mL)处理后评估 NF-κB 途径活性。与 EF24(IC5035 μM)和姜黄素(IC50>50 μM)相比,EF31(IC505 μM)对 LPS 诱导的 NF-κB DNA 结合具有显著更强的抑制作用。此外,EF31 还抑制 NF-κB 核易位以及下游炎症介质的诱导,包括促炎细胞因子 mRNA 和蛋白(肿瘤坏死因子-α、白细胞介素-1β 和白细胞介素-6)。关于这些 NF-κB 效应的机制,EF31(IC501.92 μM)对 IκB 激酶β的抑制作用明显强于 EF24(IC50131 μM)。最后,EF31 在 NF-κB 依赖性癌细胞系中表现出强大的毒性,而在 RAW264.7 巨噬细胞中则具有最小且可逆的毒性。这些数据表明,EF31 是 NF-κB 活性的更有效抑制剂,比 EF24 或姜黄素更强,同时具有抗炎和抗癌活性。因此,EF31 是一种很有前途的姜黄素类似物,可进一步开发治疗方法。