Source:http://linkedlifedata.com/resource/pubmed/id/21601767
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2011-5-23
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pubmed:abstractText |
Chronic heart failure is one of the leading causes of morbidity and mortality in Western countries and is a major financial burden to the health care system. Pharmacologic treatment and implanting devices are the predominant therapeutic approaches. They improve survival and have offered significant improvement in patient quality of life, but they fall short of producing an authentic remedy. Cardiac gene therapy, the introduction of genetic material to the heart, offers great promise in filling this void. In-depth knowledge of the underlying mechanisms of heart failure is, obviously, a prerequisite to achieve this aim. Extensive research in the past decades, supported by numerous methodological breakthroughs, such as transgenic animal model development, has led to a better understanding of the cardiovascular diseases and, inadvertently, to the identification of several candidate genes. Of the genes that can be targeted for gene transfer, calcium cycling proteins are prominent, as abnormalities in calcium handling are key determinants of heart failure. A major impediment, however, has been the development of a safe, yet efficient, delivery system. Nonviral vectors have been used extensively in clinical trials, but they fail to produce significant gene expression. Viral vectors, especially adenoviral, on the other hand, can produce high levels of expression, at the expense of safety. Adeno-associated viral vectors have emerged in recent years as promising myocardial gene delivery vehicles. They can sustain gene expression at a therapeutic level and maintain it over extended periods of time, even for years, and, most important, without a safety risk.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/HL-071763,
http://linkedlifedata.com/resource/pubmed/grant/HL-080498,
http://linkedlifedata.com/resource/pubmed/grant/HL-083156,
http://linkedlifedata.com/resource/pubmed/grant/HL-088434,
http://linkedlifedata.com/resource/pubmed/grant/HL-093183,
http://linkedlifedata.com/resource/pubmed/grant/HL-100396
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
1916-7075
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011. Published by Elsevier Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
265-83
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pubmed:meshHeading |
pubmed-meshheading:21601767-Animals,
pubmed-meshheading:21601767-Chronic Disease,
pubmed-meshheading:21601767-Clinical Trials as Topic,
pubmed-meshheading:21601767-Disease Models, Animal,
pubmed-meshheading:21601767-Female,
pubmed-meshheading:21601767-Forecasting,
pubmed-meshheading:21601767-Gene Expression Regulation,
pubmed-meshheading:21601767-Gene Therapy,
pubmed-meshheading:21601767-Gene Transfer Techniques,
pubmed-meshheading:21601767-Genetic Vectors,
pubmed-meshheading:21601767-Heart Failure,
pubmed-meshheading:21601767-Humans,
pubmed-meshheading:21601767-Male,
pubmed-meshheading:21601767-Molecular Targeted Therapy,
pubmed-meshheading:21601767-Survival Analysis,
pubmed-meshheading:21601767-Treatment Outcome,
pubmed-meshheading:21601767-United States
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pubmed:articleTitle |
Targeted gene therapy for the treatment of heart failure.
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pubmed:affiliation |
Cardiovascular Research Center, Mount Sinai School of Medicine, New York, New York, USA.
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pubmed:publicationType |
Journal Article,
Review,
Research Support, N.I.H., Extramural
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