Targeting the cell cycle machinery for the treatment of cardiovascular disease

被引:38
作者
Bicknell, KA [1 ]
Surry, EL [1 ]
Brooks, G [1 ]
机构
[1] Univ Reading, Sch Anim & Microbial Sci, Cardiovasc Res Grp, Reading RG6 6AJ, Berks, England
关键词
D O I
10.1211/002235703765344487
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cardiovascular disease represents a major clinical problem affecting a significant proportion of the world's population and remains the main cause of death in the UK. The majority of therapies currently available for the treatment of cardiovascular disease do not cure the problem but merely treat the symptoms. Furthermore, many cardioactive drugs have serious side effects and have narrow therapeutic windows that can limit their usefulness in the clinic. Thus, the development of more selective and highly effective therapeutic strategies that could cure specific cardiovascular diseases would be of enormous benefit both to the patient and to those countries where healthcare systems are responsible for an increasing number of patients. In this review, we discuss the evidence that suggests that targeting the cell cycle machinery in cardiovascular cells provides a novel strategy for the treatment of certain cardiovascular diseases. Those cell cycle molecules that are important for regulating terminal differentiation of cardiac myocytes and whether they can be targeted to reinitiate cell division and myocardial repair will be discussed as will the molecules that control vascular smooth muscle cell (VSMC) and endothelial cell proliferation in disorders such as atherosclerosis and restenosis. The main approaches currently used to target the cell cycle machinery in cardiovascular disease have employed gene therapy techniques. We will overview the different methods and routes of gene delivery to the cardiovascular system and describe possible future drug therapies for these disorders. Although the majority of the published data comes from animal studies, there are several instances where potential therapies have moved into the clinical setting with promising results.
引用
收藏
页码:571 / 591
页数:21
相关论文
共 189 条
  • [1] ABE J, 1994, CANCER RES, V54, P3407
  • [2] Adenoviral delivery of E2F-1 directs cell cycle reentry and p53-independent apoptosis in postmitotic adult myocardium in vivo
    Agah, R
    Kirshenbaum, LA
    Abdellatif, M
    Truong, LD
    Chakraborty, S
    Michael, LH
    Schneider, MD
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) : 2722 - 2728
  • [3] Cardiomyocyte-specific gene expression following recombinant adeno-associated viral vector transduction
    Aikawa, R
    Huggins, GS
    Snyder, RO
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (21) : 18979 - 18985
  • [4] *AM HEART ASS, 2003, HEART DIS STROK STAT
  • [5] High-efficiency endovascular gene delivery via therapeutic ultrasound
    Amabile, PG
    Waugh, JM
    Lewis, TN
    Elkins, CJ
    Janas, W
    Dake, MD
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (07) : 1975 - 1980
  • [6] Inhibition of the p53 tumor suppressor gene results in growth of human aortic vascular smooth muscle cells - Potential role of p53 in regulation of vascular smooth muscle cell growth
    Aoki, M
    Morishita, R
    Matsushita, H
    Hayashi, S
    Nakagami, H
    Yamamoto, K
    Moriguchi, A
    Kaneda, Y
    Higaki, J
    Ogihara, T
    [J]. HYPERTENSION, 1999, 34 (02) : 192 - 200
  • [7] LOCAL-DELIVERY OF VASCULAR ENDOTHELIAL GROWTH-FACTOR ACCELERATES REENDOTHELIALIZATION AND ATTENUATES INTIMAL HYPERPLASIA IN BALLOON-INJURED RAT CAROTID-ARTERY
    ASAHARA, T
    BAUTERS, C
    PASTORE, C
    KEARNEY, M
    ROSSOW, S
    BUNTING, S
    FERRARA, N
    SYMES, JF
    ISNER, JM
    [J]. CIRCULATION, 1995, 91 (11) : 2793 - 2801
  • [8] Isolation of putative progenitor endothelial cells for angiogenesis
    Asahara, T
    Murohara, T
    Sullivan, A
    Silver, M
    vanderZee, R
    Li, T
    Witzenbichler, B
    Schatteman, G
    Isner, JM
    [J]. SCIENCE, 1997, 275 (5302) : 964 - 967
  • [9] Axel DI, 1997, CIRCULATION, V96, P636
  • [10] Constitutive expression of phVEGF165 after intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia
    Baumgartner, I
    Pieczek, A
    Manor, O
    Blair, R
    Kearney, M
    Walsh, K
    Isner, JM
    [J]. CIRCULATION, 1998, 97 (12) : 1114 - 1123