首页> 外文期刊>BMC Genomics >A new approach to construct pathway connected networks and its application in dose responsive gene expression profiles of rat liver regulated by 2,4DNT
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A new approach to construct pathway connected networks and its application in dose responsive gene expression profiles of rat liver regulated by 2,4DNT

机译:构建途径连接网络的新方法及其在2,4DNT调节的大鼠肝脏剂量反应性基因表达谱中的应用

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BackgroundMilitary and industrial activities have lead to reported release of 2,4-dinitrotoluene (2,4DNT) into soil, groundwater or surface water. It has been reported that 2,4DNT can induce toxic effects on humans and other organisms. However the mechanism of 2,4DNT induced toxicity is still unclear. Although a series of methods for gene network construction have been developed, few instances of applying such technology to generate pathway connected networks have been reported.ResultsMicroarray analyses were conducted using liver tissue of rats collected 24h after exposure to a single oral gavage with one of five concentrations of 2,4DNT. We observed a strong dose response of differentially expressed genes after 2,4DNT treatment. The most affected pathways included: long term depression, breast cancer regulation by stathmin1, WNT Signaling; and PI3K signaling pathways. In addition, we propose a new approach to construct pathway connected networks regulated by 2,4DNT. We also observed clear dose response pathway networks regulated by 2,4DNT.ConclusionsWe developed a new method for constructing pathway connected networks. This new method was successfully applied to microarray data from liver tissue of 2,4DNT exposed animals and resulted in the identification of unique dose responsive biomarkers in regards to affected pathways.
机译:背景军事和工业活动已导致2,4-二硝基甲苯(2,4DNT)释放到土壤,地下水或地表水中。据报道,2,4DNT可以诱导对人类和其他生物的毒性作用。然而,2,4DNT诱导毒性的机制仍不清楚。尽管已经开发出了一系列构建基因网络的方法,但很少有人报道使用这种技术来生成通路连接网络的方法。结果使用暴露于单个口腔的24h收集的大鼠肝脏组织进行了微阵列分析,其中五种之一浓度为2,4DNT。我们观察到2,4DNT处理后差异表达基因的强烈剂量反应。影响最大的途径包括:长期抑郁,stathmin1,WNT信号传导调节乳腺癌;和PI3K信号通路。此外,我们提出了一种新的方法来构建受2,4DNT调控的通路连接网络。我们还观察到由2,4DNT调节的清晰的剂量反应途径网络。结论我们开发了一种构建途径连接网络的新方法。该新方法已成功应用于来自2,4DNT暴露动物肝脏组织的微阵列数据,并导致了关于受影响途径的独特剂量反应性生物标志物的鉴定。

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