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首页> 外文期刊>Planta medica: Natural products and medicinal plant research >Cytotoxicity and mode of action of four naturally occuring flavonoids from the genus Dorstenia: gancaonin Q, 4-hydroxylonchocarpin, 6-prenylapigenin, and 6,8-diprenyleriodictyol.
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Cytotoxicity and mode of action of four naturally occuring flavonoids from the genus Dorstenia: gancaonin Q, 4-hydroxylonchocarpin, 6-prenylapigenin, and 6,8-diprenyleriodictyol.

机译:背叶藻属中四种天然存在的类黄酮的细胞毒性和作用方式:gancaonin Q,4-hydroxylonchocarpin,6-prenylapigenin和6,8-diprenyleriodictyol。

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摘要

Several flavonoid-like compounds were found to possess good antiproliferative properties. Herein, we examined the ability of four naturally occuring and biologically active flavonoids from the genus Dorstenia, gancaonin Q (1), 6-prenylapigenin (2), 6,8-diprenyleriodictyol (3), and 4-hydroxylonchocarpin ( 4), to inhibit the proliferation of a panel of fourteen cancer cell lines including leukemia and solid cancer cells, as well as AML12 normal hepatocytes. The study was extended to the analysis of cell cycle distribution, apoptosis induction, and caspase 3/7 activity and the antiangiogenic properties of the four compounds. The results of the cytotoxicity assays showed that more than 50 % inhibition of proliferation was obtained with compound 1 on all the fourteen studied cancer cell lines, with IC (50) values below 20 microg/mL. Compounds 2, 4, and 3 showed selective activity, with IC (50) values below 20 microg/mL being noted on 57.15 %, 71.42 %, and 85.71 % of the fourteen cancer cell lines, respectively. None of the compounds exhibited more than 50 % inhibition against AML12 normal hepatocytes cells at 20 microg/mL. IC (50) values below or around 4 microg/mL were recorded on 28.57 % of the tested cell lines for both compound 1 and 4 and 21.43 % for compound 3, which appeared to be the best cytotoxic compounds. This study indicates that caspase 3/7 activation is one of the modes of induction of apoptosis for compounds 1, 3, and 4 in CCRF-CEM cells. The results of the antiangiogenic assay indicated that compounds 1, 3, and 4 were also able to inhibit the growth of blood capillaries on the chorioallantoic membrane of quail eggs, the best effect being noted for compound 4 (54.1 % inhibition). The results of the present work provide evidence of the cytotoxic potential of the four studied flavonoids and supportive data for further investigations.
机译:发现几种类黄酮类化合物具有良好的抗增殖特性。在这里,我们检查了来自Dorstenia属,gancaonin Q(1),6-prenylapigenin(2),6,8-diprenyleriodictyol(3)和4-hydroxylonchocarpin(4)的四种天然存在的生物活性黄酮的能力。抑制包括白血病和实体癌细胞以及AML12正常肝细胞在内的14种癌细胞系的增殖。该研究扩展至细胞周期分布,凋亡诱导和胱天蛋白酶3/7活性以及这四种化合物的抗血管生成特性的分析。细胞毒性试验的结果表明,在所有14种研究的癌细胞系中,化合物1均获得了50%以上的增殖抑制,IC(50)值低于20 microg / mL。化合物2、4和3表现出选择性活性,在14种癌细胞系中,IC(50)值分别低于20 microg / mL,分别占57.15%,71.42%和85.71%。在20 microg / mL下,没有一种化合物对AML12正常肝细胞具有超过50%的抑制作用。在化合物1和4的测试细胞系中,有28.57%的化合物的IC(50)值低于或约为4 microg / mL,化合物3的IC(50)值为21.43%,这似乎是最好的细胞毒性化合物。这项研究表明caspase 3/7激活是CCRF-CEM细胞中化合物1、3和4诱导凋亡的方式之一。抗血管生成测定的结果表明,化合物1、3和4还能够抑制鹌鹑蛋绒毛尿囊膜上毛细血管的生长,化合物4的效果最佳(抑制率为54.1%)。本工作的结果提供了四个研究类黄酮的细胞毒性潜力的证据,并为进一步研究提供了支持性数据。

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