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Cardiac Gene Therapy

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Abstract

Heart failure is a chronic progressive disorder in which frequent and recurrent hospitalizations are associated with high mortality and morbidity. The incidence and the prevalence of this disease will increase with the increase in the number of the aging population of the United States. Understanding the molecular pathology and pathophysiology of this disease will uncover novel targets and therapies that can restore the function or attenuate the damage of malfunctioning cardiomyocytes by gene therapy that becomes an interesting and a promising field for the treatment of heart failure as well as other diseases in the future. Of equal importance are developing vectors and delivery methods that can efficiently transduce most of the cardiomyocytes that can offer a long-term expression and that can escape the host immune response. Recombinant adeno-associated virus vectors have the potential to become a promising novel therapeutic vehicles for molecular medicine in the future.

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References
1.
Beeri R, Chaput M, Guerrero J, Kawase Y, Yosefy C, Abedat S . Gene delivery of sarcoplasmic reticulum calcium ATPase inhibits ventricular remodeling in ischemic mitral regurgitation. Circ Heart Fail. 2010; 3(5):627-34. PMC: 2939951. DOI: 10.1161/CIRCHEARTFAILURE.109.891184. View

2.
Carr A, Schmidt A, Suzuki Y, Monte F, Sato Y, Lanner C . Type 1 phosphatase, a negative regulator of cardiac function. Mol Cell Biol. 2002; 22(12):4124-35. PMC: 133876. DOI: 10.1128/MCB.22.12.4124-4135.2002. View

3.
Asghari P, Schulson M, Scriven D, Martens G, Moore E . Axial tubules of rat ventricular myocytes form multiple junctions with the sarcoplasmic reticulum. Biophys J. 2009; 96(11):4651-60. PMC: 2711526. DOI: 10.1016/j.bpj.2009.02.058. View

4.
Hoshijima M, Ikeda Y, Iwanaga Y, Minamisawa S, Date M, Gu Y . Chronic suppression of heart-failure progression by a pseudophosphorylated mutant of phospholamban via in vivo cardiac rAAV gene delivery. Nat Med. 2002; 8(8):864-71. DOI: 10.1038/nm739. View

5.
Rosenzweig A . Vectors for cardiovascular gene therapy. J Mol Cell Cardiol. 2003; 35(7):731-3. DOI: 10.1016/s0022-2828(03)00144-5. View