Aumsuwan Pranapda, Khan Shabana I, Khan Ikhlas A, Walker Larry A, Dasmahapatra Asok K
National Center for Natural Product Research, University of Mississippi, MS 38677, USA; Division of Pharmacology, Department of BioMolecular Sciences, University of Mississippi, MS 38677, USA.
National Center for Natural Product Research, University of Mississippi, MS 38677, USA; Division of Pharmacognosy, Department of BioMolecular sciences, School of Pharmacy, University of Mississippi, MS 38677, USA.
Data Brief. 2016 May 25;8:272-9. doi: 10.1016/j.dib.2016.05.040. eCollection 2016 Sep.
Microarray technology (Human OneArray microarray, phylanxbiotech.com) was used to compare gene expression profiles of non-invasive MCF-7 and invasive MDA-MB-231 breast cancer cells exposed to dioscin (DS), a steroidal saponin isolated from the roots of wild yam, (Dioscorea villosa). Initially the differential expression of genes (DEG) was identified which was followed by pathway enrichment analysis (PEA). Of the genes queried on OneArray, we identified 4641 DEG changed between MCF-7 and MDA-MB-231 cells (vehicle-treated) with cut-off log2 |fold change|≧1. Among these genes, 2439 genes were upregulated and 2002 were downregulated. DS exposure (2.30 μM, 72 h) to these cells identified 801 (MCF-7) and 96 (MDA-MB-231) DEG that showed significant difference when compared with the untreated cells (p<0.05). Within these gene sets, DS was able to upregulate 395 genes and downregulate 406 genes in MCF-7 and upregulate 36 and downregulate 60 genes in MDA-MB-231 cells. Further comparison of DEG between MCF-7 and MDA-MB-231 cells exposed to DS identified 3626 DEG of which 1700 were upregulated and 1926 were down-regulated. Regarding to PEA, 12 canonical pathways were significantly altered between these two cell lines. However, there was no alteration in any of these pathways in MCF-7 cells, while in MDA-MB-231 cells only MAPK pathway showed significant alteration. When PEA comparison was made on DS exposed cells, it was observed that only 2 pathways were significantly affected. Further, we identified the shared DEG, which were targeted by DS and overlapped in both MCF-7 and MDA-MB-231 cells, by intersection analysis (Venn diagram). We found that 7 DEG were overlapped of which six are reported in the database. This data highlight the diverse gene networks and pathways in MCF-7 and MDA-MB-231 human breast cancer cell lines treated with dioscin.
采用微阵列技术(人类全基因组芯片,phylanxbiotech.com)比较了非侵袭性MCF-7和侵袭性MDA-MB-231乳腺癌细胞在暴露于薯蓣皂苷(DS)后的基因表达谱。薯蓣皂苷是从野生山药(薯蓣属植物)根部分离得到的一种甾体皂苷。首先确定基因差异表达(DEG),随后进行通路富集分析(PEA)。在OneArray芯片上查询的基因中,我们确定在MCF-7和MDA-MB-231细胞(溶剂处理组)之间有4641个DEG发生变化,截断值为log2|倍数变化|≧1。在这些基因中,2439个基因上调,2002个基因下调。将这些细胞暴露于DS(2.30 μM,72小时)后,与未处理细胞相比,分别鉴定出801个(MCF-7)和96个(MDA-MB-231)显示出显著差异的DEG(p<0.05)。在这些基因集中,DS能够在MCF-7细胞中上调395个基因和下调406个基因,在MDA-MB-231细胞中上调36个基因和下调60个基因。进一步比较暴露于DS的MCF-7和MDA-MB-231细胞之间的DEG,确定了3626个DEG,其中1700个上调,1926个下调。关于PEA,这两种细胞系之间有12条经典通路发生了显著改变。然而,在MCF-7细胞中这些通路均未发生改变,而在MDA-MB-231细胞中只有丝裂原活化蛋白激酶(MAPK)通路显示出显著改变。当对暴露于DS的细胞进行PEA比较时,发现只有2条通路受到显著影响。此外,我们通过交叉分析(维恩图)确定了在MCF-7和MDA-MB-231细胞中均被DS靶向且重叠的共同DEG。我们发现有7个DEG重叠,其中6个在数据库中有报道。这些数据突出了经薯蓣皂苷处理的MCF-7和MDA-MB-231人乳腺癌细胞系中不同的基因网络和通路。