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Functional genomics annotation of a statistical epistasis network associated with bladder cancer susceptibility

机译:与膀胱癌易感性相关的统计上位网络的功能基因组学注释

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Background Several different genetic and environmental factors have been identified as independent risk factors for bladder cancer in population-based studies. Recent studies have turned to understanding the role of gene-gene and gene-environment interactions in determining risk. We previously developed the bioinformatics framework of statistical epistasis networks (SEN) to characterize the global structure of interacting genetic factors associated with a particular disease or clinical outcome. By applying SEN to a population-based study of bladder cancer among Caucasians in New Hampshire, we were able to identify a set of connected genetic factors with strong and significant interaction effects on bladder cancer susceptibility. Findings To support our statistical findings using networks, in the present study, we performed pathway enrichment analyses on the set of genes identified using SEN, and found that they are associated with the carcinogen benzo[a]pyrene, a component of tobacco smoke. We further carried out an mRNA expression microarray experiment to validate statistical genetic interactions, and to determine if the set of genes identified in the SEN were differentially expressed in a normal bladder cell line and a bladder cancer cell line in the presence or absence of benzo[a]pyrene. Significant nonrandom sets of genes from the SEN were found to be differentially expressed in response to benzo[a]pyrene in both the normal bladder cells and the bladder cancer cells. In addition, the patterns of gene expression were significantly different between these two cell types. Conclusions The enrichment analyses and the gene expression microarray results support the idea that SEN analysis of bladder in population-based studies is able to identify biologically meaningful statistical patterns. These results bring us a step closer to a systems genetic approach to understanding cancer susceptibility that integrates population and laboratory-based studies.
机译:背景技术在基于人群的研究中,已经确定了几种不同的遗传和环境因素作为膀胱癌的独立危险因素。最近的研究转向了解基因-基因和基因-环境相互作用在确定风险中的作用。我们之前开发了统计上位网络(SEN)的生物信息学框架来表征与特定疾病或临床结果相关的相互作用遗传因素的整体结构。通过将SEN应用于新罕布什尔州高加索人的一项基于人群的膀胱癌研究,我们能够确定一组相关的遗传因素,这些因素对膀胱癌的易感性具有强烈而显着的相互作用。结果为了支持使用网络的统计结果,在本研究中,我们对使用SEN鉴定的基因集进行了途径富集分析,发现它们与致癌物质苯并[a] re(烟草烟雾的一种成分)有关。我们进一步进行了mRNA表达微阵列实验,以验证统计基因的相互作用,并确定在SEN中确定的一组基因是否在存在或不存在苯并[]的正常膀胱细胞系和膀胱癌细胞系中差异表达。 ]发现来自SEN的重要非随机基因集在正常膀胱细胞和膀胱癌细胞中均响应苯并[a] py而差异表达。另外,这两种细胞类型之间的基因表达模式显着不同。结论富集分析和基因表达微阵列结果支持这样的观点,即基于人群的研究中对SEN的膀胱分析可以识别生物学上有意义的统计模式。这些结果使我们更接近采用系统遗传学方法来理解癌症易感性的方法,该方法结合了人口研究和实验室研究。

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