Therapeutic angiogenesis in cardiovascular disease

被引:246
作者
Simons, M
Ware, JA [1 ]
机构
[1] Dartmouth Coll Sch Med, Angiogenesis Res Ctr, Lebanon, NH 03756 USA
[2] Dartmouth Coll Sch Med, Cardiol Sect, Dept Med, Lebanon, NH 03756 USA
[3] Dartmouth Coll Sch Med, Dept Pharmacol & Toxicol, Lebanon, NH 03756 USA
[4] Eli Lilly & Co, Indianapolis, IN 46285 USA
关键词
D O I
10.1038/nrd1226
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Despite considerable progress in the management of ischaemic cardiovascular disease during the past three decades, there remains a significant population of patients who are not served well by current treatment approaches. Stimulating revascularization in ischaemic regions is an attractive novel therapeutic strategy, and several angiogenic agents anticipated to have the potential to achieve this goal have been clinically evaluated in recent years. However, as yet none have shown sufficient efficacy to be approved. Here, we consider the key findings from the completed clinical trials of therapeutic angiogenesis in cardiovascular disease, and discuss possible changes to the way in which such agents are developed that could improve the chances of success.
引用
收藏
页码:863 / 871
页数:9
相关论文
共 61 条
[51]   Bone marrow cells adopt the phenotype of other cells by spontaneous cell fusion [J].
Terada, N ;
Hamazaki, T ;
Oka, M ;
Hoki, M ;
Mastalerz, DM ;
Nakano, Y ;
Meyer, EM ;
Morel, L ;
Petersen, BE ;
Scott, EW .
NATURE, 2002, 416 (6880) :542-545
[52]  
Tomita N, 2000, J Atheroscler Thromb, V7, P1
[53]   Angiogenesis in ischaemic myocardium by intramyocardial autologous bone marrow mononuclear cell implantation [J].
Tse, HF ;
Kwong, YL ;
Chan, JKF ;
Lo, G ;
Ho, CL ;
Lau, CP .
LANCET, 2003, 361 (9351) :47-49
[54]   The sequential activation and repression of the human PDGF-B gene during chronic hypoxia reveals antagonistic roles for the depletion of oxygen and glucose [J].
Ullerås, E ;
Wilcock, A ;
Miller, SJ ;
Franklin, GC .
GROWTH FACTORS, 2001, 19 (04) :233-245
[55]   Effects of local MCP-1 protein therapy on the development of the collateral circulation and atherosclerosis in Watanabe hyperlipidemic rabbits [J].
van Royen, N ;
Hoefer, I ;
Buschmann, I ;
Kostin, S ;
Voskuil, M ;
Bode, C ;
Schaper, W ;
Piek, JJ .
CARDIOVASCULAR RESEARCH, 2003, 57 (01) :178-185
[56]  
Vincent KA, 2000, CIRCULATION, V102, P2255
[57]   Modulation of collateral artery growth in a porcine hindlimb ligation model using MCP-1 [J].
Voskuil, M ;
van Royen, N ;
Hoefer, IE ;
Seidler, R ;
Guth, BD ;
Bode, C ;
Schaper, W ;
Piek, JJ ;
Buschmann, IR .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2003, 284 (04) :H1422-H1428
[58]   Angiogenesis in ischemic heart disease [J].
Ware, JA ;
Simons, M .
NATURE MEDICINE, 1997, 3 (02) :158-164
[59]   In vivo myocardial gene transfer: optimization and evaluation of intracoronary gene delivery in vivo [J].
Wright, MJ ;
Wightman, LML ;
Latchman, DS ;
Marber, MS .
GENE THERAPY, 2001, 8 (24) :1833-1839
[60]   In vivo myocardial gene transfer: Optimization, evaluation and direct comparison of gene transfer vectors [J].
Wright, MJ ;
Wightman, LML ;
Lilley, C ;
de Alwis, M ;
Hart, SL ;
Miller, A ;
Coffin, RS ;
Thrasher, A ;
Latchman, DS ;
Marber, MS .
BASIC RESEARCH IN CARDIOLOGY, 2001, 96 (03) :227-236