首页> 外文期刊>Journal of Molecular Biology Research >Study of Anticancer Activity of Pratensein and Pratensein Glycoside Isolated from Cuscuta kotchiana
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Study of Anticancer Activity of Pratensein and Pratensein Glycoside Isolated from Cuscuta kotchiana

机译:从CuScuta kotchiana分离的Pratensein和Pratensein糖苷的抗癌活性研究

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In the present paper, we demonstrate that extract of Cuscuta kotchiana is able to inhibit in vitro proliferation of two human breast cancer cell lines, MCF-7 and MDA-MB-231. The expression levels of p53, bcl-2, caspase-3 and bax genes at the mRNA and protein levels were evaluated using quantitative Real Time PCR and western blot analysis. The most active fractions of C. kotchiana were detected by NMR as pratensein and pratensein glycoside. The cytotoxic activity of pratensein glycoside was significantly more than pratensein. The expression level of bcl2 gene was decreased in cancer cells treated by both compounds at CC50 concentrations. But the expression levels of caspase-3, p53 and bax genes were increased in treated cancer cells. In conclusion, all the data demonstrated that the glycoside form of pratensein is important agent in inducing apoptosis in human breast cancer cells.
机译:在本文中,我们证明Cuscuta Kotchiana的提取物能够抑制两种人乳腺癌细胞系,MCF-7和MDA-MB-231的体外增殖。使用定量实时PCR和Western印迹分析评估P53,Bcl-2,Caspase-3和MRNA和蛋白水平处的BAX基因的表达水平。 NMR作为Pratensein和Pratensein糖苷的NMR检测到最活跃的C. kotchiana。 pratensein糖苷的细胞毒性活性大于pratensein。通过在CC 50浓度处理的化合物处理的癌细胞中,BCL2基因的表达水平降低。但在处理过的癌细胞中,Caspase-3,P53和Bax基因的表达水平增加。总之,所有数据都证明了Pratensein的糖苷形式是诱导人乳腺癌细胞凋亡的重要试剂。

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