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A bioinformatics analysis to identify novel biomarkers for prognosis of pulmonary tuberculosis

机译:生物信息学分析,鉴定新型生物标志物,用于肺结核预后

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摘要

Due to the fact that pulmonary tuberculosis (PTB) is a highly infectious respiratory disease characterized by high herd susceptibility and hard to be treated, this study aimed to search novel effective biomarkers to improve the prognosis and treatment of PTB patients. Firstly, bioinformatics analysis was performed to identify PTB-related differentially expressed genes (DEGs) from GEO database, which were then subjected to GO annotation and KEGG pathway enrichment analysis to initially describe their functions. Afterwards, clustering analysis was conducted to identify PTB-related gene clusters and relevant PPI networks were established using the STRING database. Based on the further differential and clustering analyses, 10 DEGs decreased during PTB development were identified and considered as candidate hub genes. Besides, we retrospectively analyzed some relevant studies and found that 7 genes (CCL20, PTGS2, ICAM1, TIMP1, MMP9, CXCL8 and IL6) presented an intimate correlation with PTB development and had the potential serving as biomarkers. Overall, this study provides a theoretical basis for research on novel biomarkers of PTB, and helps to estimate PTB prognosis as well as probe into targeted molecular treatment.
机译:由于这样的事实:肺结核(PTB)的特点是高牛群易感性和硬一种传染性很强的呼吸道疾病被处理,这项研究旨在寻找新的有效的生物标记物,以提高肺结核患者的预后和治疗。首先,进行生物信息学分析以鉴定来自Geo数据库的PTB相关的差异表达基因(DEGS),然后进行GO注释和Kegg途径浓缩分析,以便最初描述其功能。然后,进行聚类分析以识别PTB相关的基因集群,并使用字符串数据库建立相关的PPI网络。基于进一步的差异和聚类分析,鉴定了PTB发育过程中的10次下降,并被视为候选中心基因。此外,我们回顾性地分析了一些相关研究,发现7个基因(CCL20,PTGS2,ICAM1,TIMP1,MMP9,CXCL8和IL6)呈现了与PTB发育的亲密相关性,并且具有潜在的用作生物标志物。总体而言,本研究为PTB的新型生物标志物研究提供了理论依据,有助于估计PTB预后以及探针进入靶向分子处理。

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