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首页> 外文期刊>Frontiers in Pharmacology >Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment
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Repositioning of Hypoglycemic Drug Linagliptin for Cancer Treatment

机译:降解降血糖药物Linaglitin用于癌症治疗方法

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Background Drug repositioning, development of new uses for marketed drugs, is an effective way to discover new antitumor compounds. In this study, we used a new method, filtering compounds via molecular docking to find key targets combination. Methods The data of gene expression in cancer and normal tissues of colorectal, breast, and liver cancer were obtained from The Cancer Genome Atlas Project (TCGA). The key targets combination was obtained from the protein-protein interaction network (PPI network) and the correlation analysis of the targets. Molecular docking was used to reposition the drugs which were obtained from DrugBank. MTT proliferation assay and animal experiments were used to verify the activity of candidate compounds. Flow cytometric analysis of proliferation, cell cycle and apoptosis, slice analysis, gene regulatory network, and Western blot were performed to elucidate the mechanism of drug action. Results CDK1 and AURKB were identified as a pair of key targets by the analysis of different expression gene from TCGA. Three compounds, linagliptin, mupirocin, and tobramycin, from 12 computationally predicted compounds, were verified to inhibit cell viability in HCT116 (colorectal), MCF7 (breast), and HepG2 (liver) cancer cells. Linagliptin, a hypoglycemic drug, was proved to inhibit cell proliferation by cell cycle arrest and induce apoptosis in HCT116 cells, and suppress tumor growth in nude mice bearing HCT116 cells. Linagliptin reduced the tumor size and decreased the expression of Ki67, a nuclear protein expressed in all proliferative cells. Gene regulatory network and Western blot analysis suggested that linagliptin inhibited tumor cell proliferation and promoted cell apoptosis through suppressing the expression and phosphorylation of Rb, plus down-regulating the expression of Pro-caspase3 and Bcl-2, respectively. Conclusion The combination of key targets based on the protein-protein interaction network that were built by the different gene expression of TCGA data to reposition the marketed drugs turned out to be a new approach to discover new antitumor drugs. Hypoglycemic drug linagliptin could potentially lead to novel therapeutics for the treatment of tumors, especially for colorectal cancer. Gene regulatory network is a valuable method for predicting and explaining the mechanism of drugs action.
机译:背景技术药物重新定位,销售药物的新用途的开发是一种发现新的抗肿瘤化合物的有效方法。在这项研究中,我们使用了一种新方法,通过分子对接过滤化合物以找到关键目标组合。方法从癌症基因组地图集项目(TCGA)中获得癌症和正常组织中基因表达的数据和正常组织的数据。从蛋白质 - 蛋白质相互作用网络(PPI网络)获得关键目标组合以及目标的相关分析。使用分子对接来重新定位从药物银行获得的药物。 MTT增殖测定和动物实验用于验证候选化合物的活性。流式细胞术分析的增殖,细胞周期和凋亡,切片分析,基因调节网络和蛋白质印迹进行了阐明了药物作用的机制。结果通过分析来自TCGA的不同表达基因,将CDK1和AurkB鉴定为一对关键目标。验证了来自12种计算预测化合物的三种化合物,Linagliptin,Mupirocin和毒素,以抑制HCT116(结肠直肠),MCF7(乳腺)和HepG2(肝脏)癌细胞中的细胞活力。证明了一种低血糖药物,一种低血糖药物,通过细胞周期骤停抑制细胞增殖,并在HCT116细胞中诱导细胞凋亡,并抑制携带HCT116细胞的裸鼠肿瘤生长。 Linagliptin降低了肿瘤大小并降低了Ki67的表达,在所有增殖细胞中表达的核蛋白。基因调节网络和Western印迹分析表明,Linagliptin通过抑制Rb的表达和磷酸化,加上Pro-Caspase3和Bcl-2的表达,Linagliptin抑制肿瘤细胞增殖和促进细胞凋亡。结论基于蛋白质 - 蛋白质相互作用网络的关键靶标的组合,该网络由TCGA数据的不同基因表达进行重新定位销售药物,成为发现新抗肿瘤药物的新方法。降血糖药物Linagliptin可能导致新的治疗肿瘤治疗肿瘤,特别是对于结肠直肠癌。基因调节网络是一种有价值的方法,用于预测和解释药物作用的机制。

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