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Regulation of Pharmacogene Expression by microRNA in The Cancer Genome Atlas (TCGA) Research Network

机译:MicroRNA在癌症基因组Atlas(TCGA)研究网络中的药物转基因的调节

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Individual differences in drug responses are associated with genetic and epigenetic variability of pharmacogene expression. We aimed to identify the relevant miRNAs which regulate pharmacogenes associated with drug responses. The miRNA and mRNA expression profiles derived from data for normal and solid tumor tissues in The Cancer Genome Atlas (TCGA) Research Network. Predicted miRNAs targeted to pharmacogenes were identified using publicly available databases. A total of 95 pharmacogenes were selected from cholangiocarcinoma and colon adenocarcinoma, as well as kidney renal clear cell, liver hepatocellular, and lung squamous cell carcinomas. Through the integration analyses of miRNA and mRNA, 35 miRNAs were found to negatively correlate with mRNA expression levels of 16 pharmacogenes in normal bile duct, liver, colon, and lung tissues (p<0.05). Additionally, 36 miRNAs were related to differential expression of 32 pharmacogene mRNAs in those normal and tumorigenic tissues (p<0.05). These results indicate that changes in expression levels of miRNAs targeted to pharmacogenes in normal and tumor tissues may play a role in determining individual variations in drug response.
机译:药物反应的个体差异与药物性能的遗传和表观遗传变异有关。我们的旨在鉴定调节与药物反应相关的药物的相关miRNA。 miRNA和mRNA表达谱系来自癌症基因组地图集(​​TCGA)研究网络中的正常和实体肿瘤组织数据数据。使用公开的数据库确定靶向药剂的预测miRNA。共选出95个药剂从胆管癌和结肠腺癌,以及肾肾透明细胞,肝肝细胞和肺鳞状细胞癌。通过MiRNA和mRNA的整合分析,发现35 mIRNA与正常胆管,肝脏,结肠和肺组织中16个药剂的mRNA表达水平负相关(P <0.05)。另外,36 mIRNA与32种末端和致瘤组织中的32种药物MRNA的差异表达有关(P <0.05)。这些结果表明,靶向正常和肿瘤组织中药剂的miRNA的表达水平的变化可能在确定药物反应中的个体变化方面发挥作用。

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