The pathogenesis shared between abdominal aortic aneurysms and intracranial aneurysms: a microarray analysis

医学 动脉瘤 微阵列分析技术 CCL5 趋化因子 信号转导 基因表达谱 腹主动脉瘤 生物信息学 微阵列 基因表达 发病机制 病理 基因 炎症 免疫系统 免疫学 生物 细胞生物学 遗传学 外科 T细胞 白细胞介素2受体
作者
Wen Wang,Hao Li,Zheng Zhao,Haoyuan Wang,Dong Zhang,Yan Zhang,Qing Lan,Jiangfei Wang,Yong Cao,Jizong Zhao
出处
期刊:Neurosurgical Review [Springer Science+Business Media]
卷期号:41 (2): 667-674 被引量:3
标识
DOI:10.1007/s10143-017-0912-2
摘要

Abdominal aortic aneurysms (AAAs) and intracranial saccular aneurysms (IAs) are the most common types of aneurysms. This study was to investigate the common pathogenesis shared between these two kinds of aneurysms. We collected 12 IAs samples and 12 control arteries from the Beijing Tiantan Hospital and performed microarray analysis. In addition, we utilized the microarray datasets of IAs and AAAs from the Gene Expression Omnibus (GEO), in combination with our microarray results, to generate messenger RNA expression profiles for both AAAs and IAs in our study. Functional exploration and protein-protein interaction (PPI) analysis were performed. A total of 727 common genes were differentially expressed (404 was upregulated; 323 was downregulated) for both AAAs and IAs. The GO and pathway analyses showed that the common dysregulated genes were mainly enriched in vascular smooth muscle contraction, muscle contraction, immune response, defense response, cell activation, IL-6 signaling and chemokine signaling pathways, etc. The further protein-protein analysis identified 35 hub nodes, including TNF, IL6, MAPK13, and CCL5. These hub node genes were enriched in inflammatory response, positive regulation of IL-6 production, chemokine signaling pathway, and T/B cell receptor signaling pathway. Our study will gain new insight into the molecular mechanisms for the pathogenesis of both types of aneurysms and provide new therapeutic targets for the patients harboring AAAs and IAs.
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