Molecular targets of gene therapy

Ischemic reperfused heart represents a potential target for gene therapy because gene transfer can represent an alternate pharmacological approach to protect the heart from cellular injury. Gene therapy may be particularly useful to deal with previously unapproachable problems. For myocardial preser...

Full description

Saved in:
Bibliographic Details
Published inThe Annals of thoracic surgery Vol. 68; no. 5; pp. 1929 - 1933
Main Authors Das, Dipak K, Engelman, Richard M, Maulik, Nilanjana, Rousou, John A, Flack, Joseph E, Deaton, David W
Format Journal Article Conference Proceeding
LanguageEnglish
Published New York, NY Elsevier Inc 01.11.1999
Elsevier Science
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Ischemic reperfused heart represents a potential target for gene therapy because gene transfer can represent an alternate pharmacological approach to protect the heart from cellular injury. Gene therapy may be particularly useful to deal with previously unapproachable problems. For myocardial preservation, gene therapy could replace those pharmacological interventions when drugs are delivered locally by sustained release with the help of mechanical device, eg, implants. In this review, attempts are made to define the molecular targets for gene therapy primarily applicable to myocardial preservation associated with ischemia and reperfusion. It has been emphasized that for successful gene transfer, not only characterization of proper targets and elimination of undesirable side effects are necessary, but also the therapy must be proven superior compared to other pharmacological interventions including surgery.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-3
content type line 23
ObjectType-Review-1
ISSN:0003-4975
1552-6259
DOI:10.1016/S0003-4975(99)01015-2