Literature DB >> 11715940

Cationic lipid-mediated gene transfer: current concepts.

P R Clark1, E M Hersh.   

Abstract

Infectious disease, heart disease, cancer, autoimmunity, genetic defects and even traumatic injury may someday be treated with gene therapy and gene transfer strategies. The potential impact of this new technology on human disease has produced optimism and expectation for scientists and lay people alike. As more effort is directed at harvesting the potential of this technology it has become clear that the success or failure of gene therapy will hinge on our ability to manipulate and control the process of gene transfer in somatic cells. Today, somatic gene transfer is accomplished using either viral or non-viral gene transfer methods. The benefits and limitations of each system are aggressively being investigated to determine which characteristics are most compatible with safe and reliable gene transfer. Gene transfer with cationic lipid/plasmid DNA complexes (cationic lipoplexes) has become a popular means of delivering therapeutic genes and is being tested in preclinical and clinical trials. Cationic lipoplexes are easy and inexpensive to produce, they are composed of non-toxic and non-immunogenic precursor, and they have the potential of delivering large polynucleotides into somatic cells. Additionally, these reagents are easily manipulated in the laboratory to incorporate novel biological functions or to produce new formulations that can be screened for in vivo gene transfer activity. The last few years has seen many advances in our understanding of molecular and biological factors that influence cationic lipid-mediated gene transfer. In this review we discuss recent developments in the field of cationic lipid-mediated gene transfer with emphasis on in vivo application where possible. We will consider new discoveries concerning the molecular and cellular events that control the uptake, transit and expression of lipoplexes in somatic cells. Recent biodistribution and pharmacokinetic studies and current concepts regarding the toxicity and immunogenicity of cationic lipoplexes will also be discussed. We also survey some of the many preclinical and clinical trials using cationic lipid-mediated gene transfer, with emphasis on cancer applications.

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Year:  1999        PMID: 11715940

Source DB:  PubMed          Journal:  Curr Opin Mol Ther        ISSN: 1464-8431


  13 in total

1.  The shape parameter of liposomes and DNA-lipid complexes determined by viscometry utilizing small sample volumes.

Authors:  Y Sun; X Li; N Düzgüneş; Y Takaoka; S Ohi; S Hirota
Journal:  Biophys J       Date:  2003-08       Impact factor: 4.033

Review 2.  Intracellular trafficking of plasmids for gene therapy: mechanisms of cytoplasmic movement and nuclear import.

Authors:  Erin E Vaughan; James V DeGiulio; David A Dean
Journal:  Curr Gene Ther       Date:  2006-12       Impact factor: 4.391

3.  Computational and analytical modeling of cationic lipid-DNA complexes.

Authors:  Oded Farago; Niels Grønbech-Jensen
Journal:  Biophys J       Date:  2007-01-26       Impact factor: 4.033

Review 4.  Nonviral vector gene modification of stem cells for myocardial repair.

Authors:  Husnain K Haider; Ibrahim Elmadbouh; Michel Jean-Baptiste; Muhammad Ashraf
Journal:  Mol Med       Date:  2008 Jan-Feb       Impact factor: 6.354

5.  Intrinsic bio-signature of gene delivery nanocarriers may impair gene therapy goals.

Authors:  Jaleh Barar; Yadollah Omidi
Journal:  Bioimpacts       Date:  2013-09-17

Review 6.  Functional lipids and lipoplexes for improved gene delivery.

Authors:  Xiao-Xiang Zhang; Thomas J McIntosh; Mark W Grinstaff
Journal:  Biochimie       Date:  2011-05-20       Impact factor: 4.079

7.  Bioapplications of Nanomaterials.

Authors:  Kim-Hung Huynh; Kwee-Yum Lee; Hyejin Chang; Sang Hun Lee; Jaehi Kim; Xuan-Hung Pham; Yoon-Sik Lee; Won-Yeop Rho; Bong-Hyun Jun
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

Review 8.  Real-time optical imaging using quantum dot and related nanocrystals.

Authors:  Nobuyuki Kosaka; Thomas E McCann; Makoto Mitsunaga; Peter L Choyke; Hisataka Kobayashi
Journal:  Nanomedicine (Lond)       Date:  2010-07       Impact factor: 5.307

9.  In vivo anti-tumor effect of expressing p14ARF-TAT using a FGF2-targeted cationic lipid vector.

Authors:  Guoqin Niu; Wouter H P Driessen; Sean M Sullivan; Jeffrey A Hughes
Journal:  Pharm Res       Date:  2011-01-19       Impact factor: 4.200

10.  Liquid crystalline phases of dendritic lipid-DNA self-assemblies: lamellar, hexagonal, and DNA bundles.

Authors:  Alexandra Zidovska; Heather M Evans; Kai K Ewert; Joel Quispe; Bridget Carragher; Clinton S Potter; Cyrus R Safinya
Journal:  J Phys Chem B       Date:  2009-03-26       Impact factor: 2.991

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