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AAV Mediated Angiogenic Therapy for Coronary Disease

AAV Mediated Angiogenic Therapy for Coronary Disease
AAV 介导的冠状动脉血管生成治疗
批准号:
6979799
负责人:
YUET Wai KAN
金额:
$29.59万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-12-05 至 2006-11-30

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Current treatment of coronary insufficiency with angioplasty or coronary bypass could be complicated by restenosis in about one third of the cases. The discovery of angiogenic factors that promote blood vessel growth such as VEGF and FGF has stimulated the investigation of using them for the treatment of coronary disease. Direct injection of the growth factors only produces transient effect. The gene encoding for angiogenic factors delivered in the form of plasmic DNA, or by adenoviral vectors are currently being tested. We propose to deliver the genes encoding for angiogenic factors by AAV vectors. AAV appears to be an ideal vector for the delivery of angiogenic factors as it is nonpathogenic. Intramuscular injection of AAV vectors has been shown to be an efficient way of delivering secretory proteins such as erythropoietin and Factor IX. Our preliminary studies indicate that VEGF delivered by AAV vectors into the myocardium can stimulate new blood vessel growth in the myocardium of mice with occluded coronary arteries. The aims of this proposal are: (1) We will verify and extend these preliminary findings by using a rat model in addition to the mouse; rat because the pathophysiologic consequences of coronary occlusion are better understood and the techniques for measuring them well established; and mice because the 3 dimensional structure of the coronary vasculature can be visualized by a new CT technique. Effect of AAV delivered angiogenic factors on left ventricular functions will be determined by echocardiography and measurement with the pressure-volume catheter. (2) We will regulate the expression of the genes for angiogenic factors to avoid over expression, which may cause angioma formation. The hypoxia responsive element of the Epo and VEGF gene will first be investigated. Alternatively, other inducible system will also be tested. (3) We will compare the effectiveness of AAV delivery of the genes for VEGF and angiopoietins, alone and in different combinations. These studies may lead to an effective approach for the treatment of coronary insufficiency.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
AAV serotype 1 mediates more efficient gene transfer to pig myocardium than AAV serotype 2 and plasmid.
AAV 血清型 1 比 AAV 血清型 2 和质粒更有效地介导向猪心肌的基因转移。
DOI: 10.1002/jgm.1129
发表时间: 2008
期刊: The journal of gene medicine
影响因子: --
作者: [Su,H, Yeghiazarians,Y, Lee,A, Huang,Y, Arakawa-Hoyt,J, Ye,J, Orcino,G, Grossman,W, Kan,YW]
通讯作者: Kan,YW
Adeno-associated viral vector delivers cardiac-specific and hypoxia-inducible VEGF expression in ischemic mouse hearts.
腺相关病毒载体在缺血小鼠心脏中传递心脏特异性和缺氧诱导的 VEGF 表达。
DOI: 10.1073/pnas.0407449101
发表时间: 2004
期刊: Proceedings of the National Academy of Sciences of the United States of America.
影响因子: --
作者: [Su,Hua, Joho,Shuji, Huang,Yu, Barcena,Alicia, Arakawa-Hoyt,Janice, Grossman,William, Kan,YuetWai]
通讯作者: Kan,YuetWai
DOI: 10.1007/978-1-59745-030-0_19
发表时间: 2007
期刊: Methods in molecular biology
影响因子: --
作者: [H. Su;Y. Kan]
通讯作者: H. Su;Y. Kan
Reprogramming iPS Cells with Exogenous and Endogenous Transcription Factor Genes
Reprogramming iPS Cells with Exogenous and Endogenous Transcription Factor Genes
Development of iPS Cells for Treatment of Hemoglobinopathies
Development of iPS Cells for Treatment of Hemoglobinopathies
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