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作 者:艾瑞婷[1] 吴少瑜[1] 文晓芸[1] 徐伟[1] 吕琳[1] 吴曙光[1]
出 处:《中药材》2011年第11期1734-1740,共7页Journal of Chinese Medicinal Materials
基 金:国家自然科学基金(30901823);广东省自然科学基金(9151051501000088);广东高校优秀青年创新人才培育项目(LYM09039);广东省优秀博士资助项目(sybzzxm201044)
摘 要:目的:研究从日本蛇菰中分离的天然多酚化合物1,2,6-三-O-没食子酰基-β-D-吡喃葡萄糖(BJA32531)对人肝癌细胞HepG2增殖的抑制作用以及对miRNA表达的影响。方法:采用CCK-8的方法检测HepG2细胞的增殖;用流式细胞法检测HepG2细胞的凋亡;采用miRNA芯片分析方法测定HepG2细胞的miRNA表达以及用RT-PCR的方法验证miRNA的表达。结果:BJA32531以时间和剂量依赖的方式抑制HepG2细胞的增殖;流式细胞结果表明:该化合物能引起HepG2细胞的凋亡。miRNA芯片结果显示,BJA32531能诱导HepG2细胞19个miRNA的表达上调以及85个miRNA的表达下调。RT-PCR验证了化合物诱导的let-7a和miR-10b的上调以及miR-132和miR-125b的下调与芯片的结果一致。结论:BJA32531抗HepG2细胞增殖作用的机理可能与调控miRNA的表达有关。Objective:To study the effect of 1,2,6-Tri-O-galloyl-β-D-glucopyranose(BJA32531) on the miRNA expression during BJA32531-induced cytotoxicity in human HepG2 hepatocarcinoma cells.Methods:Cell proliferation was assessed using a colorimetric assay(cell counting kit-8).Apoptosis was assessed by annexin V and propidium iodide staining.The miRNA expression profile of the cancer cells was analyzed by a miRNA array and quantitative real-time PCR.Results: BJA32531 inhibited the cell proliferation and increased apoptosis in HepG2 cancer cells.Cellular exposure to BJA32531 influenced the miRNA expression pattern in the cells,including 19 upregulated and 85 down-regulated miRNAs in the cells.The up-regulations of let-7a and miR-10b as well as the down-regulations of miR-132 and miR-125b were verified to be consistent with the the results of the miRNA array.Conclusion: Our study suggests that the mechanisms by which BJA32531 exerted the antiproliferative effects on HepG2 cancer cells may be related to its regulation of miRNA.
关 键 词:MIRNA 人肝癌HEPG2细胞 细胞增殖 多酚化合物 BJA32531
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