Chen L, Fan Y, Wan J
Department of Neurosurgery, Ren Ji Hospital, Shanghai Jiao Tong University, Shanghai, China.
Department of Neurosurgery, Ren Ji Hospital, Shanghai Jiao Tong University, Shanghai, China
Genet Mol Res. 2014 Jan 31;13(1):758-67. doi: 10.4238/2014.January.31.2.
This study aimed to identify differentially expressed genes (DEGs) of unruptured intracranial aneurysms (IAs) and provide beneficial information for early diagnosis and treatment of IAs. The gene expression profile GSE26969 from the Gene Expression Omnibus database was downloaded, which included six human IA samples: three intracranial arterial aneurysm samples and three normal superficial temporal artery samples (control). Based on these data, we identified the DEGs between normal and disease samples with packages in the R language. The selected DEGs were further analyzed using bioinformatic methods. First, the STRING software was used to search co-expression relationships among DEGs, and the most important hub gene was found. We then used the plugins of the Cytoscape software, Mcode and Bingo, to conduct a module analysis. Next, pathways of the module genes were annotated using the FuncAssociate program. Compared with the control group, we obtained 169 DEGs in total, and by mining a module with the hub gene MYH11, we retrieved the ACTA2, MYH11, MYLK, and MYL9 genes, which were all in the module and were most significantly related to vascular smooth muscle contraction. We hypothesize that the genes identified here can be beneficial for early diagnosis and treatment of IAs.
本研究旨在鉴定未破裂颅内动脉瘤(IA)的差异表达基因(DEG),并为IA的早期诊断和治疗提供有益信息。从基因表达综合数据库下载了基因表达谱GSE26969,其中包括6个人类IA样本:3个颅内动脉瘤样本和3个正常颞浅动脉样本(对照)。基于这些数据,我们使用R语言中的软件包鉴定正常样本和疾病样本之间的DEG。对选定的DEG进一步采用生物信息学方法进行分析。首先,使用STRING软件搜索DEG之间的共表达关系,找出最重要的枢纽基因。然后我们使用Cytoscape软件的插件Mcode和Bingo进行模块分析。接下来,使用FuncAssociate程序对模块基因的通路进行注释。与对照组相比,我们总共获得了169个DEG,通过挖掘以枢纽基因MYH11为中心的一个模块,我们找到了ACTA2、MYH11、MYLK和MYL9基因,这些基因都在该模块中,并且与血管平滑肌收缩最显著相关。我们推测,这里鉴定出的基因可能有助于IA的早期诊断和治疗。