首页> 外文期刊>Journal of Medicinal Plants Research >A possible molecular mechanism of two flavones and two flavonols on the induction of differentiation in a human oesophageal adenocarcinoma cell line (OE33)
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A possible molecular mechanism of two flavones and two flavonols on the induction of differentiation in a human oesophageal adenocarcinoma cell line (OE33)

机译:两种黄酮和两种黄酮醇可能诱导人食道腺癌细胞系(OE33)分化的分子机制

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摘要

The influences of two flavones (baicalein, chrysin) and two flavonols (galangin, kaempferol) selected on induction of differentiation in a human esophageal adenocarcinoma (OE33) cell line were studied in the present work. All compounds selected could be able to inhibit proliferation of OE33 cells in a dose- and time-dependent manner. The inhibitory potency of these compounds on OE33 cells was in the order of: galangin?>?chrysin?>?baicalein?>kaempferol. OE33 cells treated with these compounds for 24 h showed differentiation characteristics including the differentiation-specific morphological changes, the augmentation of differentiation markers and the inhibition of human telomerase reverse transcriptase. The potency of these compounds on induction of differentiation of OE33 cells was similar to that of them on growth inhibition.?To reveal the possible molecular mechanisms by which these compounds?modulate?proliferation and?differentiation?in OE33 cells,?the alterations of three genes, 14-3-3s, cyclin B1 and cyclin D1, which are related to proliferation and differentiation of cells,?were investigated?by real-time polymerase chain reaction (RT-PCR) and Western blot. The results showed that up-regulation of 14-3-3s?and down-regulation of cyclin B1 and cyclin D1 at the mRNA and protein levels were observed in OE33 cells treated with these compounds, indicating that 14-3-3s, cyclin B1 and cyclin D1 might be target genes of these flavonoids in inducing differentiation of OE33 cells.
机译:在本研究中,研究了两种黄酮(黄ical苷,黄ry苷)和两种黄酮醇(高良姜精,山emp酚)对人食管腺癌(OE33)细胞分化诱导的影响。选择的所有化合物都可能能够以剂量和时间依赖性的方式抑制OE33细胞的增殖。这些化合物对OE33细胞的抑制力的顺序为:高良姜精→胰蛋白酶→黄ical苷→山emp酚。用这些化合物处理24小时的OE33细胞显示出分化特征,包括分化特异性形态变化,分化标志物的增强和对人类端粒酶逆转录酶的抑制。这些化合物在诱导OE33细胞分化中的效能与它们在生长抑制方面的效能相似。通过实时聚合酶链反应(RT-PCR)和蛋白质印迹研究了与细胞增殖和分化有关的基因14-3-3s,细胞周期蛋白B1和细胞周期蛋白D1。结果表明,在用这些化合物处理的OE33细胞中,观察到14-3-3s的上调和cyclin B1和cyclin D1在mRNA和蛋白水平的下调,表明14-3-3s,cyclin B1 cyclin D1可能是这些类黄酮诱导OE33细胞分化的靶基因。

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