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The search for common pathways underlying asthma and COPD

机译:寻找哮喘和COPD的常见途径

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Abstract: Recently, several genes and genetic loci associated with both asthma and chronic obstructive pulmonary disease (COPD) have been described as common susceptibility factors for the two diseases. In complex diseases such as asthma and COPD, a large number of molecular and cellular components may interact through complex networks involving gene–gene and gene–environment interactions. We sought to understand the functional and regulatory pathways that play central roles in the pathobiology of asthma and COPD and to understand the overlap between these pathways. We searched the PubMed database up to September 2012 to identify genes found to be associated with asthma, COPD, tuberculosis, or essential hypertension in at least two independent reports of candidate-gene associations or in genome-wide studies. To learn how the identified genes interact with each other and other cellular proteins, we conducted pathway-based analysis using Ingenuity Pathway Analysis software. We identified 108 genes and 58 genes that were significantly associated with asthma and COPD in at least two independent studies, respectively. These susceptibility genes were grouped into networks based on functional annotation: 12 (for asthma) and eleven (for COPD) networks were identified. Analysis of the networks for overlap between the two diseases revealed that the networks form a single complex network with 229 overlapping molecules. These overlapping molecules are significantly involved in canonical pathways including the “aryl hydrocarbon receptor signaling,” “role of cytokines in mediating communication between immune cells,” “glucocorticoid receptor signaling,” and “IL-12 signaling and production in macrophages” pathways. The Jaccard similarity index for the comparison between asthma and COPD was 0.81 for the network-level comparison, and the odds ratio was 3.62 (P < 0.0001) for the asthma/COPD pair in comparison with the tuberculosis/ essential hypertension pair. In conclusion, although the identification of asthma and COPD networks is still far from complete, these networks may be used as frameworks for integrating other genome-scale information including expression profiling and phenotypic analysis. Network overlap between asthma and COPD may indicate significant overlap between the pathobiology of these two diseases, which are thought to be genetically related.
机译:摘要:最近,与哮喘和慢性阻塞性肺疾病(COPD)相关的几种基因和遗传位点已被描述为两种疾病的常见易感性因素。在诸如哮喘和COPD之类的复杂疾病中,大量分子和细胞成分可能通过涉及基因-基因和基因-环境相互作用的复杂网络相互作用。我们试图了解在哮喘和COPD病理生物学中起关键作用的功能和调节途径,并了解这些途径之间的重叠。我们搜索了截至2012年9月的PubMed数据库,以至少在两项独立的候选基因关联报告或全基因组研究中鉴定与哮喘,COPD,肺结核或原发性高血压相关的基因。为了了解鉴定出的基因如何与其他细胞蛋白相互作用,我们使用了Ingenuity Pathway Analysis软件进行了基于路径的分析。在至少两项独立研究中,我们分别鉴定出与哮喘和COPD显着相关的108个基因和58个基因。根据功能注释,将这些易感基因分组为网络:识别了12个(对于哮喘)和11个(对于COPD)网络。对两种疾病之间重叠的网络的分析表明,这些网络形成了一个具有229个重叠分子的单一复杂网络。这些重叠的分子显着参与了经典途径,包括“芳基烃受体信号传导”,“细胞因子在免疫细胞之间的介导交流中的作用”,“糖皮质激素受体信号传导”以及“ IL-12信号传导和巨噬细胞产生”。对于网络水平的比较,哮喘与COPD的比较的Jaccard相似性指数为0.81,而与结核病/原发性高血压对相比,哮喘/ COPD对的优势比为3.62(P <0.0001)。总之,尽管哮喘和COPD网络的鉴定还很不完善,但这些网络可以用作整合其他基因组规模信息(包括表达谱和表型分析)的框架。哮喘和COPD之间的网络重叠可能表明这两种疾病的病理生物学之间存在明显的重叠,这被认为与遗传有关。

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