首页> 外文期刊>Archives of Biochemistry and Biophysics >The anticancer potential of steroidal saponin, dioscin, isolated from wild yam (Dioscorea villosa) root extract in invasive human breast cancer cell line MDA-MB-231 in vitro
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The anticancer potential of steroidal saponin, dioscin, isolated from wild yam (Dioscorea villosa) root extract in invasive human breast cancer cell line MDA-MB-231 in vitro

机译:从野生山药(Dioscorea villosa)根提取物中分离的甾体皂苷,薯os皂素在浸润性人乳腺癌细胞系MDA-MB-231中的体外抗癌能力

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摘要

Previously, we observed that wild yam (Dioscorea villosa) root extract (WYRE) was able to activate GATA3 in human breast cancer cells targeting epigenome. This study aimed to find out if dioscin (DS), a bioactive compound of WYRE, can modulate GATA3 functions and cellular invasion in human breast cancer cells. MCF-7 and MDA-MB-231 cells were treated in the absence/presence of various concentrations of DS and subjected to gene analysis by RT-qPCR, immunoblotting, and immunocytochemistry. We determined the ability of MDA-MB-231 cells to migrate into wound area and examined the effects of DS on cellular invasion using invasion assay. DS reduced cell viability of both cell lines in a concentration and time dependent manner. GATA3 expression was enhanced by DS (5.76 mu M) in MDA-MB-231 cells. DS (5.76 mu M)-treated MDA-MB-231 cells exhibited the morphological characteristic of epithelial-like cells; mRNA expression of DNMT3A, TET2, TET3, ZFPM2 and E-cad were increased while TET1, VIM and MMP9 were decreased. Cellular invasion of MDA-MB-231 was reduced by 65 5% in the presence of 5.76 mu M DS. Our data suggested that DS-mediated pathway could promote GATA3 expression at transcription and translation levels. We propose that DS has potential to be used as an anti-invasive agent in breast cancer. Published by Elsevier Inc.
机译:以前,我们观察到野生山药(Dioscorea villosa)根提取物(WYRE)能够激活靶向表观基因组的人乳腺癌细胞中的GATA3。这项研究旨在发现薯di皂甙(DS)(一种WYRE的生物活性化合物)是否可以调节人乳腺癌细胞中的GATA3功能和细胞侵袭。在不存在/存在各种浓度DS的情况下处理MCF-7和MDA-MB-231细胞,并通过RT-qPCR,免疫印迹和免疫细胞化学进行基因分析。我们确定了MDA-MB-231细胞迁移到伤口区域的能力,并使用侵袭试验检查了DS对细胞侵袭的影响。 DS以浓度和时间依赖性方式降低了两种细胞系的细胞活力。 DS(5.76μM)在MDA-MB-231细胞中增强了GATA3表达。 DS(5.76μM)处理的MDA-MB-231细胞表现出上皮样细胞的形态特征。 DNMT3A,TET2,TET3,ZFPM2和E-cad的mRNA表达增加,而TET1,VIM和MMP9的mRNA表达减少。在存在5.76μM DS的情况下,MDA-MB-231的细胞侵袭减少了65 5%。我们的数据表明,DS介导的途径可以在转录和翻译水平上促进GATA3表达。我们建议DS有潜力在乳腺癌中用作抗侵袭剂。由Elsevier Inc.发布

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