Genetic targeting for cardiovascular therapeutics: are we near the summit or just beginning the climb?

Published online

Journal Article (Review)

This article is based on an Experimental Biology symposium held in April 2001 and presents the current status of gene therapy for cardiovascular diseases in experimental studies and clinical trials. Evidence for the use of gene therapy to limit neointimal hyperplasia and confer myocardial protection was presented, and it was found that augmenting local nitric oxide (NO) production using gene transfer (GT) of NO synthase or interruption of cell cycle progression through a genetic transfer of cell cycle regulatory genes limited vascular smooth muscle hyperplasia in animal models and infra-inguinal bypass patients. The results of application of vascular endothelial growth factor (VEGF) GT strategies for therapeutic angiogenesis in critical limb and myocardial ischemia in pilot clinical trials was reviewed. In addition, experimental evidence was presented that genetic manipulation of peptide systems (i.e., the renin-angiotensin II system and the kallikrein-kinin system) was effective in the treatment of systemic cardiovascular diseases such as hypertension, heart failure, and renal failure. Although, as of yet, there are no well controlled human trials proving the clinical benefits of gene therapy for cardiovascular diseases, the data presented here in animal models and in human subjects show that genetic targeting is a promising and encouraging modality, not only for the treatment and long-term control of cardiovascular diseases, but for their prevention as well.

Full Text

Duke Authors

Cited Authors

  • Francis, SC; Raizada, MK; Mangi, AA; Melo, LG; Dzau, VJ; Vale, PR; Isner, JM; Losordo, DW; Chao, J; Katovich, MJ; Berecek, KH

Published Date

  • December 21, 2001

Published In

Volume / Issue

  • 7 / 2

Start / End Page

  • 79 - 94

PubMed ID

  • 11773594

Pubmed Central ID

  • 11773594

Electronic International Standard Serial Number (EISSN)

  • 1531-2267

Digital Object Identifier (DOI)

  • 10.1152/physiolgenomics.00073.2001

Language

  • eng

Conference Location

  • United States