Kapral Małgorzata, Sośnicki Stanisław, Wawszczyk Joanna, Węglarz Ludmiła
Acta Pol Pharm. 2014 Nov-Dec;71(6):987-93.
The aim of the present study was to examine the influence of IP6, a naturally occurring phytochem- ical, on the expression of genes coding for proliferation markers, i.e., cyclin D1 (CCND1) and histone H3 in IL-1β-stimulated intestinal cancer cell line Caco-2. Quantification of genes expression was carried out using real time RT-QPCR technique in Caco-2 cells after treatment with IL-1β, 1 and 2.5 mM of IP6 for 3, 6 and 12 h. In separate cultures, cells were incubated with IL-1β for the indicated times. The untreated Caco-2 cells were used as the control. In a time course experiment, stimulation of cells with IL-1β only resulted in an overex- pression of both CCND1 and histone H3 mRNAs as compared with control. IP6 had no influence on IL-1β-stimulated CCND1 expression for 3 and 6 h. After 12 h, statistically significant decrease in CCND1 mRNA was observed in cells exposed to IL-1β and IP6 (1 and 2.5 mM) in relation to cells treated with IL-1β only. The levels of H3 mRNA in IL-1β-stimulated cells and cells treated with IL-1β and IP6 revealed no statistically significant differences after 3 h. IP6 at 1 and 2.5 mM enhanced IL1β-stimulated transcription of H3 gene after 6 h. Subsequently (12 h), the combination of IP6 and IL-1β decreased H3 mRNA level compared to IL1β-treated cells. In conclusion, pro-inflammatory cytokine IL-1β up-regulates CCND1 and histone H3 mRNAs expression in Caco-2 cells. These results suggest that the ability of IP6 to inhibit colon cancer cells proliferation may be mediated through downregulation of genes encoding cyclin D1 and histone H3 at the mRNA level.
本研究的目的是检测天然存在的植物化学物质肌醇六磷酸(IP6)对白细胞介素-1β(IL-1β)刺激的肠癌细胞系Caco-2中增殖标志物编码基因,即细胞周期蛋白D1(CCND1)和组蛋白H3表达的影响。在用IL-1β、1 mM和2.5 mM IP6处理3、6和12小时后,使用实时逆转录定量聚合酶链反应(RT-QPCR)技术对Caco-2细胞中的基因表达进行定量。在单独培养中,细胞与IL-1β孵育指定时间。未处理的Caco-2细胞用作对照。在时间进程实验中,与对照相比,仅用IL-1β刺激细胞导致CCND1和组蛋白H3 mRNA均过表达。IP6在3和6小时对IL-1β刺激的CCND1表达没有影响。12小时后,与仅用IL-1β处理的细胞相比,暴露于IL-1β和IP6(1 mM和2.5 mM)的细胞中观察到CCND1 mRNA有统计学意义的下降。在3小时后,IL-1β刺激的细胞以及用IL-1β和IP6处理的细胞中H3 mRNA水平没有统计学意义的差异。1 mM和2.5 mM的IP6在6小时后增强了IL-1β刺激的H3基因转录。随后(12小时),与IL-1β处理的细胞相比,IP6和IL-1β的组合降低了H3 mRNA水平。总之,促炎细胞因子IL-1β上调Caco-2细胞中CCND1和组蛋白H3 mRNA的表达。这些结果表明,IP6抑制结肠癌细胞增殖的能力可能是通过在mRNA水平下调细胞周期蛋白D1和组蛋白H3编码基因来介导的。