Design and development of polymer conjugates as anti-angiogenic agents

被引:71
作者
Segal, Ehud [1 ]
Satchi-Fainaro, Ronit [1 ]
机构
[1] Tel Aviv Univ, Sackler Sch Med, Dept Physiol & Pharmacol, IL-69978 Tel Aviv, Israel
基金
以色列科学基金会;
关键词
TARGETED DRUG-DELIVERY; TUMOR ENDOTHELIAL-CELLS; WATER-SOLUBLE POLYMER; HPMA COPOLYMER; IN-VIVO; PHASE-I; NEOVASCULAR THERAPY; ENHANCED PERMEABILITY; POLYETHYLENE-GLYCOL; GENE DELIVERY;
D O I
10.1016/j.addr.2009.06.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Angiogenesis, the formation of new blood vessels from pre-existing vasculature, is one of the central key steps in tumor progression and metastasis. Consequently, it became an important target in cancer therapy, making novel angiogenesis inhibitors a new modality of anticancer agents. Although relative to conventional chemotherapy, anti-angiogenic agents display a safer toxicity profile, the vast majority of these agents are low-molecular-weight compounds exhibiting poor pharmacokinetic profile with short half-life in the bloodstream and high overall clearance rate. The "Polymer Therapeutics" field has significantly improved the therapeutic potential of low-molecular-weight drugs and proteins for cancer treatment. Drugs can be conjugated to polymeric carriers that can be either directly conjugated to targeting proteins or peptides or derivatized with adapters conjugated to a targeting moiety. This approach holds a significant promise for the development of new targeted anti-angiogenic therapies as well as for the optimization of existing anti-angiogenic drugs or polypeptides. Here we overview the innovative approach of targeting tumor angiogenesis using polymer therapeutics. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1159 / 1176
页数:18
相关论文
共 170 条
[1]  
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3582
[2]  
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3578
[3]   Molecular targeting of angiogenesis [J].
Alessi, P ;
Ebbinghaus, C ;
Neri, D .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 2004, 1654 (01) :39-49
[4]   Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model [J].
Arap, W ;
Pasqualini, R ;
Ruoslahti, E .
SCIENCE, 1998, 279 (5349) :377-380
[5]   Targeting the prostate for destruction through a vascular address [J].
Arap, W ;
Haedicke, W ;
Bernasconi, M ;
Kain, R ;
Rajotte, D ;
Krajewski, S ;
Ellerby, HM ;
Bredesen, DE ;
Pasqualini, R ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1527-1531
[6]   Anti-neovascular therapy by liposomal DPP-CNDAC targeted to angiogenic vessels [J].
Asai, T ;
Shimizu, K ;
Kondo, M ;
Kuromi, K ;
Watanabe, K ;
Ogino, K ;
Taki, T ;
Shuto, S ;
Matsuda, A ;
Oku, N .
FEBS LETTERS, 2002, 520 (1-3) :167-170
[7]   Antineovascular therapy with angiogenic vessel-targeted polyethyleneglycol-shielded liposomal DPP-CNDAC [J].
Asai, Tomohiro ;
Miyazawa, Souichiro ;
Maeda, Noriyuki ;
Hatanaka, Kentaro ;
Katanasaka, Yasufumi ;
Shimizu, Kosuke ;
Shuto, Satoshi ;
Oku, Naoto .
CANCER SCIENCE, 2008, 99 (05) :1029-1033
[8]   Rational design of a potent, long-lasting form of interferon:: A 40 kDa branched polyethylene glycol-conjugated interferon α-2a for the treatment of hepatitis C [J].
Bailon, P ;
Palleroni, A ;
Schaffer, CA ;
Spence, CL ;
Fung, WJ ;
Porter, JE ;
Ehrlich, GK ;
Pan, W ;
Xu, ZX ;
Modi, MW ;
Farid, A ;
Berthold, W .
BIOCONJUGATE CHEMISTRY, 2001, 12 (02) :195-202
[9]   A novel noninvasive model of endometriosis for monitoring the efficacy of antiangiogenic therapy [J].
Becker, Christian M. ;
Wright, Renee D. ;
Satchi-Fainaro, Ronit ;
Funakoshi, Tae ;
Folkman, Judah ;
Kung, Andrew L. ;
D'Amato, Robert J. .
AMERICAN JOURNAL OF PATHOLOGY, 2006, 168 (06) :2074-2084
[10]   Angiogenesis inhibition by angiostatin, endostatin and TNP-470 prevents cyclophosphamide induced cystitis [J].
Beecken W.-D. ;
Engl T. ;
Blaheta R. ;
Bentas W. ;
Achilles E.-G. ;
Jonas D. ;
Shing Y. ;
Camphausen K. .
Angiogenesis, 2004, 7 (1) :69-73