Title Meta-Analysis of Microarray-Based Expression Profiles to Identify Differentially Expressed Genes in Intracranial Aneurysms
Authors Xu, Zhe
Li, Hao
Song, Jiangman
Han, Bing
Wang, Zheng
Cao, Yong
Wang, Shuo
Zhao, Jizong
Affiliation Capital Med Univ, Monogen Dis Res Ctr Neurol Disorders, Beijing Tiantan Hosp, Beijing, Peoples R China.
Capital Med Univ, Core Lab Clin Med Res, Beijing Tiantan Hosp, Beijing, Peoples R China.
Capital Med Univ, Beijing Tiantan Hosp, Dept Neurosurg, Beijing, Peoples R China.
China Natl Clin Res Ctr Neurol Dis, Beijing, Peoples R China.
Peking Univ, Peoples Hosp, Dept Neurol, Beijing, Peoples R China.
Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA.
City Hope Natl Med Ctr, Beckman Res Inst, Dept Radiat Biol, Duarte, CA USA.
Capital Med Univ, Beijing Tiantan Hosp, Dept Neurosurg, Beijing, Peoples R China.
Zhao, JZ (reprint author), China Natl Clin Res Ctr Neurol Dis, Beijing, Peoples R China.
Keywords Contraction
Gene expression
Inflammation
Intracranial aneurysm
Meta-analysis
Microarray
Rupture
CEREBRAL ANEURYSMS
PROBE LEVEL
ANGIOGENESIS
RUPTURE
VEGF
INFLAMMATION
PROMOTE
GROWTH
INJURY
WALLS
Issue Date 2017
Publisher WORLD NEUROSURGERY
Citation WORLD NEUROSURGERY.2017,97,661-+.
Abstract OBJECTIVE: To gain comprehensive insight into the molecular mechanism of formation and rupture of intracranial aneurysms (IAs). METHODS: All publicly accessible microarray-based whole-genome gene expression profiles on IAs were retrieved. The significance analysis of microarrays method was applied to identify differentially expressed genes (DEGs). Functional annotation was performed using gene ontology terms and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses. Expression of DEGs was examined using quantitative polymerase chain reaction. RESULTS: Six data sets of 3 microarray platforms were qualified and analyzed. Comparing expression profiles between aneurysmal wall and control vessels, 5232 significant DEGs were identified among 3 platforms, and MMP12 was shown to have the largest fold change of upregulation. In all 3 platforms, 46 DEGs were shared, and 1297 DEGs were commonly resolved in at least 2 microarray platforms. Among these 1297 concordant DEGs, the 512 upregulated genes were mainly enriched in inflammatory and immune response processes, whereas the 785 downregulated genes were primarily concentrated in smooth muscle cell contraction and development pathways. Comparison between expression profiles of ruptured and unruptured IAs revealed that a few angiogenic factors, including HIF1A, VEGFA, and ANGPTL4, were upregulated in ruptured aneurysms. Subsequently, the upregulation of MMP12, HIF1A, and VEGFA was partially confirmed using quantitative polymerase chain reaction among independent samples. CONCLUSIONS: Inflammation, immune response, and loss of contractile vascular smooth muscle cells could potentially contribute to the formation of IAs, whereas the role of angiogenesis and vascular remodeling in IA formation and rupture needs further exploration.
URI http://hdl.handle.net/20.500.11897/476308
ISSN 1878-8750
DOI 10.1016/j.wneu.2016.10.093
Indexed SCI(E)
Appears in Collections: 人民医院

Files in This Work
There are no files associated with this item.

Web of Science®


0

Checked on Last Week

Scopus®



Checked on Current Time

百度学术™


0

Checked on Current Time

Google Scholar™





License: See PKU IR operational policies.