Differential gene expression in human cerebrovascular malformations

被引:72
作者
Shenkar, R
Elliott, JP
Diener, K
Gault, J
Hu, LJ
Cohrs, RJ
Phang, T
Hunter, L
Breeze, RE
Awad, IA
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Neurosurg, Ctr Cellular & Mol Neurosurg, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Pharmacol, Ctr Computat Pharmacol, Denver, CO 80262 USA
[3] Univ Colorado, Hlth Sci Ctr, Dept Neurol, Denver, CO 80262 USA
关键词
arteriovenous malformations; cavernous malformations; gene arrays; gene expression;
D O I
10.1227/01.NEU.0000044131.03495.22
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: We sought to identify genes with differential expression in cerebral cavernous malformations (CCMs), arteriovenous malformations (AVMs), and control superficial temporal arteries (STAs) and to confirm differential expression of genes previously implicated in the pathobiology of these lesions. METHODS: Total ribonucleic acid was isolated from four CCM, four AVM, and three STA surgical specimens and used to quantify lesion-specific messenger ribonucleic acid expression levels on human gene arrays. Data were analyzed with the use of two separate methodologies: gene discovery and confirmation analysis. RESULTS: The gene discovery method identified 42 genes that were significantly up-regulated and 36 genes that were significantly down-regulated in CCMs as compared with AVMs and STAs (P = 0.006). Similarly, 48 genes were significantly, up-regulated and 59 genes were significantly down-regulated in AVMs as compared with CCMs and STAs (P = 0.006). The confirmation analysis showed, significant differential expression (P < 0.05) in 11 of 15 genes (angiogenesis factors, receptors, and structural proteins) that previously had been reported to be expressed differentially in CCMs and AVMs in immunohistochemical analysis. CONCLUSION: We identify numerous genes that are differentially expressed in CCMs and AVMs and correlate expression with the immunohistochemistry, of genes implicated in cerebrovascular malformations. In future efforts, we will aim to confirm candidate genes specifically related to the pathobiology of cerebrovascular malformations and determine their biological systems and mechanistic relevance.
引用
收藏
页码:465 / 477
页数:13
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