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首页> 外文期刊>International immunopharmacology >Curcumin attenuates carcinogenesis by down regulating proinflammatory cytokine interleukin-1 (IL-1α and IL-1β) via modulation of AP-1 and NF-IL6 in lymphoma bearing mice
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Curcumin attenuates carcinogenesis by down regulating proinflammatory cytokine interleukin-1 (IL-1α and IL-1β) via modulation of AP-1 and NF-IL6 in lymphoma bearing mice

机译:姜黄素可通过调节AP-1和NF-IL6抑制荷瘤小鼠的促炎性细胞因子白介素1(IL-1α和IL-1β)从而减轻致癌作用。

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摘要

Interleukin-1 (IL-1α and IL-1β) is a prototypic, potent, multifunctional proinflammatory cytokine affecting almost all cell types. Expression of IL-1 is up regulated in different tumor phenotypes and is implicated as an important factor in tumor progression via expression of metastatic, angiogenic genes and growth factors. Therefore, down regulation of expression of IL-1 may be able to inhibit cancer progression. Mechanism of transcriptional regulation of mouse IL-1α is not yet reported. AP-1 binding site at - 12 to - 6 on human IL-1α promotor is highly conserved in rat IL-1α gene and regulates its expression. Based on in silico analysis, regions - 12 to - 6 bp is found to be conserved in human and mouse IL-1α gene promotor and therefore selected to study activation of IL-1α. Further, the regions - 12 to - 6 bp in mouse IL-1α gene promotor corresponding to AP-1 binding element show 3′ → 5′ orientation, necessary for AP-1 binding. The present work is focused on long term effect of curcumin on expression of IL-1α and IL-1β in liver of lymphoma bearing mice. Transcriptional regulation of IL-1α and IL-1β was analyzed by AP-1 and NF-IL-6 respectively. Elevated expression and protein level of IL-1α and IL-1β were found in lymphoma bearing mice compared to normal, which were significantly down regulated by curcumin treatment. Similarly, curcumin treatment down regulated activation of IL-1α and IL-1β via AP-1 and NF-IL-6 respectively. The findings conclude that curcumin attenuates carcinogenesis by down regulating proinflammatory cytokine interleukin-1 (IL-1α and IL-1β) via modulation of AP-1 and NF-IL6 respectively in lymphoma bearing mice.
机译:白细胞介素-1(IL-1α和IL-1β)是一种原型,有效的多功能促炎细胞因子,几乎影响所有细胞类型。 IL-1的表达在不同的肿瘤表型中被上调,并通过转移性,血管生成基因和生长因子的表达被认为是肿瘤进展的重要因素。因此,下调IL-1的表达可能能够抑制癌症的进展。小鼠IL-1α的转录调控机制尚未见报道。在人IL-1α启动子的-12至-6处的AP-1结合位点在大鼠IL-1α基因中高度保守,并调节其表达。根据计算机分析,发现在人和小鼠IL-1α基因启动子中保守的区域为12到6 bp,因此选择该区域来研究IL-1α的激活。此外,小鼠IL-1α基因启动子中与AP-1结合元件相对应的-12至6 bp区域显示了AP-1结合所必需的3'→5'方向。目前的工作集中在姜黄素对荷瘤淋巴瘤小鼠肝脏中IL-1α和IL-1β表达的长期影响。 AP-1和NF-IL-6分别分析了IL-1α和IL-1β的转录调控。与正常人相比,在淋巴瘤小鼠中发现了IL-1α和IL-1β的表达和蛋白水平升高,姜黄素治疗显着下调了它们的表达。同样,姜黄素治疗分别通过AP-1和NF-IL-6下调IL-1α和IL-1β的激活。这些发现得出结论,姜黄素可通过分别调节荷瘤小鼠的AP-1和NF-IL6来下调促炎性细胞因子白介素1(IL-1α和IL-1β)来减轻致癌作用。

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