Polymer genomics: shifting the gene and drug delivery paradigms

被引:81
作者
Kabanov, AV
Batrakova, EV
Sriadlbhatla, S
Yang, ZH
Kelly, DL
Alakov, VY
机构
[1] Univ Nebraska, Med Ctr, Inst Res Canc & Allied Dis, Coll Pharm & Eppley,Pharmaceut Sci Dept, Omaha, NE 68198 USA
[2] Supratek Pharma Inc, Dorval, PQ H9S 1A9, Canada
关键词
anthracycline antibiotics; block copolymer; cancer; gene delivery; gene expression; multidrug resistance; P-glycoprotein; poloxamer;
D O I
10.1016/j.jconrel.2004.07.009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Pluronic, the A-B-A amphiphilic block copolymers of poly(ethylene oxide) and poly(propylene oxide), can up-regulate the expression of selected genes in cells and alter genetic responses to antineoplastic agents in cancer. Two key new findings are discussed in relation to current drug and gene delivery strategies. First, these block copolymers alone and in combination with a polycation, polyethyleneimine, can up-regulate the expression of reporter genes in stably transfected cells. This underscores the ability of selected synthetic polymers to enhance transgene expression through a mechanism that augments improved DNA delivery into a cell. Second, although, when used alone, Pluronic is "genetically benign," when combined with an antineoplastic agent, doxorubicin, it drastically alters pharmacogenomic responses to this agent and prevents the development of multidrug resistance in breast cancer cells. Collectively, these Studies propose the need for a thorough assessment of pharmacogenomic effects of polymer therapeutics to maximize the clinical outcomes and understand the pharmacological and toxicological effects of polymer-based drugs and delivery systems. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:259 / 271
页数:13
相关论文
共 83 条
[1]   Block copolymeric biotransport carriers as versatile vehicles for drug delivery [J].
Alakhov, V ;
Klinski, E ;
Lemieux, P ;
Pietrzynski, G ;
Kabanov, A .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2001, 1 (04) :583-602
[2]   Hypersensitization of multidrug resistant human ovarian carcinoma cells by pluronic P85 block copolymer [J].
Alakhov, VY ;
Moskaleva, EY ;
Batrakova, EV ;
Kabanov, AV .
BIOCONJUGATE CHEMISTRY, 1996, 7 (02) :209-216
[3]  
Allison A C, 1990, Semin Immunol, V2, P369
[4]   Understanding drug release from poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) gels [J].
Anderson, BC ;
Pandit, NK ;
Mallapragada, SK .
JOURNAL OF CONTROLLED RELEASE, 2001, 70 (1-2) :157-167
[5]   Enhancement of the polycation-mediated DNA uptake and cell transfection with pluronic P85 block copolymer [J].
Astafieva, I ;
Maksimova, I ;
Lukanidin, E ;
Alakhov, V ;
Kabanov, A .
FEBS LETTERS, 1996, 389 (03) :278-280
[6]   Fundamental relationships between the composition of Pluronic block copolymers and their hypersensitization effect in MDR cancer cells [J].
Batrakova, E ;
Lee, S ;
Li, S ;
Venne, A ;
Alakhov, V ;
Kabanov, A .
PHARMACEUTICAL RESEARCH, 1999, 16 (09) :1373-1379
[7]  
Batrakova EV, 2001, J PHARMACOL EXP THER, V299, P483
[8]   Optimal structure requirements for pluronic block copolymers in modifying P-glycoprotein drug efflux transporter activity in bovine brain microvessel endothelial cells [J].
Batrakova, EV ;
Li, S ;
Alakhov, VY ;
Miller, DW ;
Kabanov, AV .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2003, 304 (02) :845-854
[9]   Pluronic P85 increases permeability of a broad spectrum of drugs in polarized BBMEC and Caco-2 cell monolayers [J].
Batrakova, EV ;
Li, S ;
Miller, DW ;
Kabanov, AV .
PHARMACEUTICAL RESEARCH, 1999, 16 (09) :1366-1372
[10]   Sensitization of cells overexpressing multidrug-resistant proteins by Pluronic P85 [J].
Batrakova, EV ;
Li, S ;
Alakhov, VY ;
Elmquist, WF ;
Miller, DW ;
Kabanov, AV .
PHARMACEUTICAL RESEARCH, 2003, 20 (10) :1581-1590