Cardiac gene therapy: are we there yet?

被引:22
作者
Matkar, P. N. [1 ,2 ]
Leong-Poi, H. [1 ,2 ]
Singh, K. K. [2 ,3 ,4 ]
机构
[1] St Michaels Hosp, Keenan Res Ctr Biomed Sci, Dept Cardiol, Toronto, ON, Canada
[2] St Michaels Hosp, Dept Vasc Surg, Keenan Res Ctr Biomed Sci, Toronto, ON, Canada
[3] St Michaels Hosp, Dept Vasc Surg, Toronto, ON, Canada
[4] St Michaels Hosp, Dept Cardiac Surg, Keenan Res Ctr Biomed Sci, Toronto, ON, Canada
关键词
ENDOTHELIAL GROWTH-FACTOR; CHRONIC MYOCARDIAL-ISCHEMIA; CALCIUM UP-REGULATION; IN-VIVO; TRANSGENE EXPRESSION; HEART-FAILURE; ADENOVIRAL VECTOR; DOUBLE-BLIND; TRANSIENT IMMUNOSUPPRESSION; CARDIOVASCULAR-DISEASES;
D O I
10.1038/gt.2016.43
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The incidence of cardiovascular disease (CVD) is increasing throughout the world and is associated with elevated morbidity and mortality. Gene therapy to treat cardiac dysfunction is gaining importance because of the limited therapeutic benefit offered by pharmacotherapies. The growing knowledge of the complex signaling pathways and the development of sophisticated vectors and delivery systems, are facilitating identification and targeting of specific molecular candidates involved in initiation and progression of CVDs. Several preclinical and clinical studies have shown the therapeutic efficiency of gene therapy in different disease models and patients. Hence, gene therapy might plausibly become an unconventional treatment modality for CVD patients. In this review, we summarize the gene delivery carriers, modes of delivery, recent preclinical/ clinical studies and potential therapeutic targets. We also briefly discuss the existing limitations of gene therapy, technical challenges surrounding gene carriers and delivery systems, and some approaches to overcome these limitations for bringing CVD gene therapy one step closer to reality.
引用
收藏
页码:635 / 648
页数:14
相关论文
共 154 条
  • [1] Gene transfer into muscle by electroporation in vivo
    Aihara, H
    Miyazaki, J
    [J]. NATURE BIOTECHNOLOGY, 1998, 16 (09) : 867 - 870
  • [2] Effect of stromal-cell-derived factor 1 on stem-cell homing and tissue regeneration in ischaemic cardiomyopathy
    Askari, AT
    Unzek, S
    Popovic, ZB
    Goldman, CK
    Forudi, F
    Kiedrowski, M
    Rovner, A
    Ellis, SG
    Thomas, JD
    DiCorleto, PE
    Topol, EJ
    Penn, MS
    [J]. LANCET, 2003, 362 (9385) : 697 - 703
  • [3] Aurélie D, 2013, CURR DRUG TARGETS, V14, P1336
  • [4] Gene therapy for restenosis - Getting nearer the heart of the matter
    Baek, S
    March, KL
    [J]. CIRCULATION RESEARCH, 1998, 82 (03) : 295 - 305
  • [5] Designing gene delivery vectors for cardiovascular gene therapy
    Baker, AH
    [J]. PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2004, 84 (2-3) : 279 - 299
  • [6] Prevention of vein graft failure: potential applications for gene therapy
    Baker, AH
    Mehta, D
    George, SJ
    Angelini, GD
    [J]. CARDIOVASCULAR RESEARCH, 1997, 35 (03) : 442 - 450
  • [7] Cell-specific targeting of lipid-based carriers for ODN and DNA
    Bartsch, M
    Weeke-Klimp, AH
    Meijer, DKF
    Scherphof, GL
    Kamps, JAAM
    [J]. JOURNAL OF LIPOSOME RESEARCH, 2005, 15 (1-2) : 59 - 92
  • [8] Adeno-Associated Virus (AAV) Serotype 9 Provides Global Cardiac Gene Transfer Superior to AAV1, AAV6, AAV7, and AAV8 in the Mouse and Rat
    Bish, Lawrence T.
    Morine, Kevin
    Sleeper, Meg M.
    Sanmiguel, Julio
    Wu, Di
    Gao, Guangping
    Wilson, James M.
    Sweeney, H. Lee
    [J]. HUMAN GENE THERAPY, 2008, 19 (12) : 1359 - 1368
  • [9] Heart Failure in North America
    Blair, John E. A.
    Huffman, Mark
    Shah, Sanjiv J.
    [J]. CURRENT CARDIOLOGY REVIEWS, 2013, 9 (02) : 128 - 146
  • [10] Myocardial gene transfer by selective pressure-regulated retroinfusion of coronary veins
    Boekstegers, P
    von Degenfeld, G
    Giehrl, W
    Heinrich, D
    Hullin, R
    Kupatt, C
    Steinbeck, G
    Baretton, G
    Middeler, G
    Katus, H
    Franz, WM
    [J]. GENE THERAPY, 2000, 7 (03) : 232 - 240