Literature DB >> 12084235

Gene therapy: future therapy for erectile dysfunction.

G Schenk1, A Melman, G Christ.   

Abstract

Advances in molecular biological techniques, completion of the Human Genome Project, and the ensuing age of molecular medicine, in conjuction with the sum of a decades-long accumulation of knowledge of the physiology of erection and the pathophysiology of erectile dysfunction have converged to make gene therapy for erectile dysfunction a distinct possibility. In short, both the intrinsic complexities of mechanisms responsible for ensuring normal erection and the multifactorial nature of erectile dysfunction ensure that there is a relatively vast number of physiologically relevant molecular targets for gene therapy. As such, perhaps it is not surprising that virtually every preclinical gene therapy strategy/target examined thus far has been largely successful in ameliorating conditions associated with compromised erectile function in vivo and/or in vitro. This report highlights the goals and strategies of gene therapy for erectile dysfunction and reviews the strategies that initially have been employed. In short, the preclinical data, while still quite preliminary in many regards, are nonetheless quite impressive and encouraging. If similar success is obtained in clinical trials, gene therapy for erectile dysfunction may provide the first concrete "proof of concept" for using gene therapy in the treatment of human smooth muscle disorders.

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Mesh:

Year:  2001        PMID: 12084235     DOI: 10.1007/s11934-001-0043-7

Source DB:  PubMed          Journal:  Curr Urol Rep        ISSN: 1527-2737            Impact factor:   2.862


  16 in total

Review 1.  Erectile dysfunction.

Authors:  T F Lue
Journal:  N Engl J Med       Date:  2000-06-15       Impact factor: 91.245

2.  Nitric oxide synthase gene therapy for erectile dysfunction: comparison of plasmid, adenovirus, and adenovirus-transduced myoblast vectors.

Authors:  S Tirney; C E Mattes; N Yoshimura; T Yokayama; H Ozawa; E Tzeng; L A Birder; A J Kanai; J Huard; W C de Groat; M B Chancellor
Journal:  Mol Urol       Date:  2001

3.  The effect of adeno-associated virus mediated brain derived neurotrophic factor in an animal model of neurogenic impotence.

Authors:  M E Bakircioglu; C S Lin; P Fan; K D Sievert; Y W Kan; T F Lue
Journal:  J Urol       Date:  2001-06       Impact factor: 7.450

4.  Gene transfer of endothelial nitric oxide synthase to the penis augments erectile responses in the aged rat.

Authors:  H C Champion; T J Bivalacqua; A L Hyman; L J Ignarro; W J Hellstrom; P J Kadowitz
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

Review 5.  Physiology of penile erection.

Authors:  K E Andersson; G Wagner
Journal:  Physiol Rev       Date:  1995-01       Impact factor: 37.312

6.  Cloning of rat and human inducible penile nitric oxide synthase. Application for gene therapy of erectile dysfunction.

Authors:  H Garbán; D Marquez; T Magee; J Moody; T Rajavashisth; J A Rodríguez; A Hung; D Vernet; J Rajfer; N F González-Cadavid
Journal:  Biol Reprod       Date:  1997-04       Impact factor: 4.285

7.  Impact of erectile dysfunction on quality of life: patient and partner perspectives.

Authors:  G Wagner; K S Fugl-Meyer; A R Fugl-Meyer
Journal:  Int J Impot Res       Date:  2000-10       Impact factor: 2.896

8.  Intracorporal injection of hSlo cDNA in rats produces physiologically relevant alterations in penile function.

Authors:  G J Christ; J Rehman; N Day; L Salkoff; M Valcic; A Melman; J Geliebter
Journal:  Am J Physiol       Date:  1998-08

9.  Gene therapy: future strategies and therapies.

Authors:  G J Christ
Journal:  Drugs Today (Barc)       Date:  2000 Feb-Mar       Impact factor: 2.245

10.  Impotence and its medical and psychosocial correlates: results of the Massachusetts Male Aging Study.

Authors:  H A Feldman; I Goldstein; D G Hatzichristou; R J Krane; J B McKinlay
Journal:  J Urol       Date:  1994-01       Impact factor: 7.450

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