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破裂与未破裂囊状颅内动脉瘤的基因表达分析。

Gene expression analysis of ruptured and un-ruptured saccular intracranial aneurysm.

机构信息

Department of Neurosurgery, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

出版信息

Eur Rev Med Pharmacol Sci. 2013 May;17(10):1374-81.

Abstract

BACKGROUND

Although Saccular intracranial aneurysm (sIA) is the most common type abnormality of all intracranial aneurysms, the biological mechanisms of sIA are not fully understood.

METHODS

We downloaded microarray datasets from Gene Expression Omnibus (GEO) database which includes 11 ruptured intracranial aneurysm samples and 8 unruptured intracranial aneurysm samples. Significant Analysis of Microarray (SAM) was employed to identify the differentially expressed genes (DEGs) between ruptured and unruptured intracranial aneurysms.

RESULTS

We found 2129 genes differentially expressed in rupture sIA, of which 1062 genes up-regulated and 1057 genes down-regulated. Functional analysis demonstrated these genes were significantly associated with inflammatory response, wounding response and defense response. Protein-protein interaction (PPI) analysis revealed that these genes may play important roles in the pathogenesis of sIAs. Results suggested that four transcription factors (TFs) could cooperated with each other, together with several microRNAs play roles in the pathonegensis of ruptured sIAs.

CONCLUSIONS

All of above results indicate the existence of DEGs between ruptured and unruptured sIAs, which regulating the pathogenesis of ruptured sIAs. TFs and microRNAs may also play key roles in ruptured sIAs. This research hints a new thought to the therapy of ruptured sIAs.

摘要

背景

尽管囊状颅内动脉瘤(sIA)是所有颅内动脉瘤中最常见的类型异常,但 sIA 的生物学机制尚未完全阐明。

方法

我们从基因表达综合数据库(GEO)下载了微阵列数据集,其中包括 11 个破裂颅内动脉瘤样本和 8 个未破裂颅内动脉瘤样本。采用显著分析微阵列(SAM)方法鉴定破裂和未破裂颅内动脉瘤之间的差异表达基因(DEGs)。

结果

我们发现破裂 sIA 中有 2129 个基因差异表达,其中 1062 个基因上调,1057 个基因下调。功能分析表明这些基因与炎症反应、创伤反应和防御反应显著相关。蛋白质-蛋白质相互作用(PPI)分析表明,这些基因可能在 sIA 的发病机制中发挥重要作用。结果表明,四个转录因子(TFs)可以相互合作,与几个 microRNAs 一起在破裂 sIA 的发病机制中发挥作用。

结论

所有这些结果表明,破裂和未破裂 sIA 之间存在差异表达基因,这些基因调节破裂 sIA 的发病机制。TFs 和 microRNAs 也可能在破裂 sIA 中发挥关键作用。这项研究为破裂 sIA 的治疗提供了新的思路。

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