Estimation of Susceptibility to and Prognosis of Cardiovascular Diseases Based on Genetic Polymorphism and Its Application to Drug Discoveries
Estimation of Susceptibility to and Prognosis of Cardiovascular Diseases Based on Genetic Polymorphism and Its Application to Drug Discoveries
批准号:
12794012
负责人:
NAGAI Ryozo
金额:
$25.66万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for University and Society Collaboration
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2002
中文摘要
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英文摘要
The aim of this study is to identify useful genetic markers associated with susceptibility to or severity of cardiovascular diseases. At first we established clinical database system for the patients in our department and we obtained DNA samples from them after informed consent by the way approved by the institutional ethics committee. Using these clinical data and genetic samples we obtained the results mentioned as follows.(l) The Met823Ile polymorphism in ABCA1 gene was one of the independent determinants of high-density lipoprotein in Japanese population. (2) The combination in the promoter SNPs of MMP1 and MMP3 was significantly associated with susceptibility to myocardial infarction. (3) The (GC)n polymorphism in HO-1 gene was associated with coronary artery diseases. (4) There was no association between glycoprotein Ia polymorphism and onset of myocardial infarction. (5) Mild hyperhomocyteinemia caused endothelial dysfunction resulting in more severe atherosclerotic lesions in rat balloon injury model. This is relevant to our previous report that genetic polymorphism in MTHFR was related to atherothrombotic diseases by affecting plasma homocysteine levels. (6) After immunohistchemical study of post-atherectomy specimens, the expression of KLF5 was shown to be a useful marker to predict post-angioplasty restenosis. Moreover we established and analyzed heterozygous KLF5-knockout mice, demonstrating that KLF5 is a key element linking external stress and cardiovascular remodeling.By promoting the genetic analyzes about important genes in cardiovascular system, we will make personalized medicine a reality after applying useful genetic markers to clinical diagnosis or guidance.
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Hoshino Y, et al.: "Regulated Expression of the BTEB2 Transcription Factor in Vascular Smooth Muscle Cells : Analysis of Developmental and Pathological Expression Profiles Shows Implications as a Predictive Factor for Restenosis"Circulation. 102. 2528-253
Hoshino Y 等人:“血管平滑肌细胞中 BTEB2 转录因子的调节表达:发育和病理表达谱的分析表明其作为再狭窄的预测因素”循环。
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通讯作者:
Itoh T, Kikuchi K, Odagawa Y, Takata S, Yano K, Okada S, Haneda N, Ogawa S, Nakano O, Kawahara Y, Kasai H, Nakayama T, Fukutomi T, Sakurada H, Shimizu A, Yazaki Y, Nagai R, Nakamura Y, Tanaka T.: "Correlation of genetic etiology with response to b-adrener
伊藤 T、菊池 K、小田川 Y、高田 S、矢野 K、冈田 S、羽田 N、小川 S、中野 O、川原 Y、葛西 H、中山 T、福富 T、樱田 H、清水 A、矢崎 Y、永井 R
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Shindo, T.: "Kruppel-like zinc-finger transcription factor KLF5/BTEB2 is a target for angiotensin II signaling and an essential regulator of cardiovascular remodeling"Nature Medicine. 8・8. 856-863 (2002)
Shindo, T.:“Kruppel 样锌指转录因子 KLF5/BTEB2 是血管紧张素 II 信号传导的靶标和心血管重塑的重要调节剂”Nature Medicine 8・8 (2002)。
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Kaneda H, et al.: "Heme oxygenase-1 gene promoter polymorphism is associated with coronary artery disease in Japanese patients with coronary risk factors"Arterioscler Thromb Vasc Biol.. 22:16. 80-85 (2002)
Kaneda H 等人:“血红素加氧酶-1 基因启动子多态性与具有冠状动脉危险因素的日本患者的冠状动脉疾病相关”Arterioscler Thromb Vasc Biol.. 22:16。
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Maemura K, et al.: "Perrell MA. Nagai R. Lee ME. Molecular mechanisms of morning onset of myocardial infarction"Ann NYAcad Sci.. 947. 398-402 (2001)
Maemura K 等:“Perrell MA. Nagai R. Lee ME. 心肌梗塞早晨发作的分子机制”Ann NYAcad Sci.. 947. 398-402 (2001)
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共 25 条
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Molecular mechanisms of phenotypic modulation and growth of smooth muscle cells
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Pathogenesis and molecular mechanisms of arteral restenosis
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Diffcrential diagnosis of tuberculosis and nontuberculous infectious diseases by PCR-RFLP and sequence-specific oligonucleotide probes
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