Microarray analysis for cerebral aneurysm-by using the information of genome
Project/Area Number |
17591533
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Cerebral neurosurgery
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Research Institution | Tokyo Women's Medical University |
Principal Investigator |
KASUYA Hidetoshi Tokyo Women's Medical University, Department of Neurosurgery, Assistant Professor, 医学部, 講師 (50169455)
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Co-Investigator(Kenkyū-buntansha) |
AKAGAWA Hiroyuki Tokyo Women's Medical University, Department of Neurosurgery, Lecturer, 医学部, 助手 (60398807)
INOUE Ituro Tokyo University, Institute of Medical Science, Division of Genetic Diagnosis, Associate Professor, 医科学研究所, 客員助教授 (00192500)
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Project Period (FY) |
2005 – 2006
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Project Status |
Completed (Fiscal Year 2006)
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Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 2005: ¥2,200,000 (Direct Cost: ¥2,200,000)
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Keywords | subarachnoid hemorrhage / aneurysm / gene expression / microarray / genome / 遺伝子 |
Research Abstract |
Using a dye swap technique, tissue samples of six ruptured and four unruptured aneurysms, as well as four cerebral arteries serving as controls, were profiled using oligonucleotide microarrays. Differentially expressed genes were extracted comparing the expression ratio between the aneurysm and control tissue and were subsequently classified according to three different grouping techniques. Gene ontology classification of the differentially expressed genes was calculated as a function integrated into GeneSpring software version 7.3 (Agilent Technologies). Identification of specific regulatory functional networks and canonical pathways was achieved by importing the differentially expressed gene list into a network-based computational pathway analysis tool (Ingenuity Systems). Analysis of the transcriptomic expression between all aneurysms, ruptured and unruptured, and control tissue revealed 521 differentially expressed genes after multiple testing correction. When comparing both tissues the most significantly associated gene ontology (GO) term within the "biological process" classification was antigen processing (GO:30333) (P=1 -64E-16), a subordinate to immune response (GO:6955) (P=3 -75E-15). The network-based analysis showed that the top scoring network was built around overexpressed major histocompatibility class (MHC) I and II complex related genes, displaying high level functions in immune response, cell-to-cell signaling, and immune and lymphatic system development and function. It further identified the MHC II related antigen presentation canonical pathway as one of the key functions that is upregulated in intracranial aneurysm tissue (P=7 -3E-10).
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Report
(3 results)
Research Products
(18 results)
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[Journal Article] A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms.2006
Author(s)
Akagawa H, Tajima A, Sakamoto Y, Krischek B, Yoneyama T, Kasuya H, Onda H, Hori T, Kubota M, Machida T, Saeki N, Hata A, Hashiguchi K, Kimura E, Kim CJ, Yang TK, Kimm K, Inoue I
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Journal Title
Hum Mol Genet 15
Pages: 1722-1734
Description
「研究成果報告書概要(欧文)」より
Related Report
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