Literature DB >> 18370200

Delivery of DNA into muscle for treating systemic diseases: advantages and challenges.

Capucine Trollet1, Daniel Scherman, Pascal Bigey.   

Abstract

An efficient and safe method to deliver DNA in vivo is a requirement for several purposes, such as the study of gene function and gene therapy applications. Among the different nonviral delivery methods currently under investigation, in vivo DNA electrotransfer has proven to be one of the most efficient and simple methods. This technique is a physical method of gene delivery consisting of a local application of electric pulses after injection of DNA. This technique can be applied to almost any tissue of a living animal, including tumors, skin, liver, kidney, artery, retina, cornea, or even brain, but the focus of this review will be on electrotransfer of plasmid DNA into skeletal muscle and its possible therapeutic uses for systemic diseases. Skeletal muscle is a good target for electrotransfer of DNA because of the following features: a large volume of easily accessible tissue, an endocrine organ capable of expressing several local and systemic factors, and muscle fibers as postmitotic cells have a long lifespan, which allows long-term gene expression. In this review, we will describe the main characteristics of DNA electrotransfer, including toxicity and safety issues related to this technique. We will focus on the important possible therapeutic applications of electrotransfer for systemic diseases demonstrated in animal models in the recent years, in the fields of monogenic diseases, tissue-specific diseases, metabolic disorders, immune-system-related diseases, and cancer. Finally, we will discuss the advantages and challenges of this technique.

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Year:  2008        PMID: 18370200     DOI: 10.1007/978-1-59745-194-9_14

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

1.  Expression of dog microdystrophin in mouse and dog muscles by gene therapy.

Authors:  Christophe Pichavant; Pierre Chapdelaine; Daniel G Cerri; Jean-Christophe Dominique; Simon P Quenneville; Daniel Skuk; Joe N Kornegay; João Cs Bizario; Xiao Xiao; Jacques P Tremblay
Journal:  Mol Ther       Date:  2010-02-23       Impact factor: 11.454

Review 2.  Electroporation for the delivery of DNA-based vaccines and immunotherapeutics: current clinical developments.

Authors:  Angela M Bodles-Brakhop; Richard Heller; Ruxandra Draghia-Akli
Journal:  Mol Ther       Date:  2009-02-17       Impact factor: 11.454

Review 3.  Gene electrotransfer: from biophysical mechanisms to in vivo applications : Part 2 - In vivo developments and present clinical applications.

Authors:  Jean-Michel Escoffre; Chloé Mauroy; Thomas Portet; Luc Wasungu; Aurelie Paganin-Gioanni; Muriel Golzio; Justin Teissié; Marie-Pierre Rols
Journal:  Biophys Rev       Date:  2009-11-10

4.  Pre-clinical toxicity assessment of tumor-targeted interleukin-12 low-intensity electrogenetherapy.

Authors:  S D Reed; S Li
Journal:  Cancer Gene Ther       Date:  2011-01-14       Impact factor: 5.987

5.  BDNF is a mediator of glycolytic fiber-type specification in mouse skeletal muscle.

Authors:  Julien Delezie; Martin Weihrauch; Geraldine Maier; Rocío Tejero; Daniel J Ham; Jonathan F Gill; Bettina Karrer-Cardel; Markus A Rüegg; Lucía Tabares; Christoph Handschin
Journal:  Proc Natl Acad Sci U S A       Date:  2019-07-18       Impact factor: 11.205

6.  APOBEC3A catabolism of electroporated plasmid DNA in mouse muscle.

Authors:  A Kostrzak; M Henry; P L Demoyen; S Wain-Hobson; J-P Vartanian
Journal:  Gene Ther       Date:  2014-10-09       Impact factor: 5.250

Review 7.  Current status of pharmaceutical and genetic therapeutic approaches to treat DMD.

Authors:  Christophe Pichavant; Annemieke Aartsma-Rus; Paula R Clemens; Kay E Davies; George Dickson; Shin'ichi Takeda; Steve D Wilton; Jon A Wolff; Christine I Wooddell; Xiao Xiao; Jacques P Tremblay
Journal:  Mol Ther       Date:  2011-04-05       Impact factor: 11.454

  7 in total

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