Homing peptides as targeted delivery vehicles

被引:118
作者
Laakkonen, Pirjo [1 ,2 ,3 ]
Vuorinen, Kirsi [1 ]
机构
[1] Univ Eastern Finland, Novel Target Mol Res Grp, Dept Biotechnol & Mol Med, AI Virtanen Inst Mol Sci, Kuopio, Finland
[2] Univ Helsinki, Biomedicum Helsinki, Inst Biomed, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Mol & Canc Biol Res Program, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
TUMOR-NECROSIS-FACTOR; ADVANCED SOLID TUMORS; VIVO PHAGE DISPLAY; IN-VIVO; FACTOR-ALPHA; ENDOTHELIAL-CELLS; AMINOPEPTIDASE N; MOUSE MODEL; PHASE-I; PHENOTYPIC HETEROGENEITY;
D O I
10.1039/c0ib00013b
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Each normal organ and pathological condition appear to contain organ- or disease-specific molecular tags on its vasculature, which constitute a vascular "zip code" system. In vivo phage display has been exploited to profile this vascular heterogeneity and a number of peptides that home specifically to various normal organs or pathological conditions have been identified. These peptides have been used for targeted delivery of oligonucleotides, drugs, imaging agents, inorganic nanoparticles, liposomes, and viruses. Identification of the receptor molecules for the homing peptides has revealed novel biomarkers for target organs. In tumors many of these receptors seem to play a functional role in tumor angiogenesis. Recently, tumor homing peptides have entered clinical trials. Results from several Phase I and II trials have been reported, and a number of trials are currently ongoing or recruiting patients. In these trials no dose-limiting toxicity has occurred and all combinations of peptide-targeted therapies have been well tolerated.
引用
收藏
页码:326 / 337
页数:12
相关论文
共 95 条
[1]   Phenotypic heterogeneity of the endothelium I. Structure, function, and mechanisms [J].
Aird, William C. .
CIRCULATION RESEARCH, 2007, 100 (02) :158-173
[2]   Phenotypic heterogeneity of the endothelium II. Representative vascular beds [J].
Aird, William C. .
CIRCULATION RESEARCH, 2007, 100 (02) :174-190
[3]   Nanocrystal targeting in vivo [J].
Åkerman, ME ;
Chan, WCW ;
Laakkonen, P ;
Bhatia, SN ;
Ruoslahti, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12617-12621
[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]   Cellular abnormalities of blood vessels as targets in cancer [J].
Baluk, P ;
Hashizume, H ;
McDonald, DM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2005, 15 (01) :102-111
[7]   Vasculature targeted tumor necrosis factor-alpha increases the therapeutic index of doxorubicin against prostate cancer [J].
Bertilaccio, Maria T. S. ;
Grioni, Matteo ;
Sutherland, Brent W. ;
Degl'Innocenti, Elena ;
Freschi, Massimo ;
Jachetti, Elena ;
Greenberg, Norman M. ;
Corti, Angelo ;
Bellone, Matteo .
PROSTATE, 2008, 68 (10) :1105-1115
[8]   cNGR: A novel homing sequence for CD13/APN targeted molecular imaging of murine cardiac angiogenesis in vivo [J].
Buehler, Alexandra ;
van Zandvoort, Marc A. M. J. ;
Stelt, Bram J. ;
Hackeng, Tilman M. ;
Schrans-Stassen, Bianca H. G. J. ;
Bennaghmouch, Abdelkader ;
Hofstra, Leo ;
Cleutjens, Jack P. M. ;
Duijvestijn, Adriaan ;
Smeets, Mirjam B. ;
de Kleijn, Dominique P. V. ;
Post, Mark J. ;
de Muinck, Ebo D. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2006, 26 (12) :2681-2687
[9]  
Burg MA, 1999, CANCER RES, V59, P2869
[10]   Angiogenesis in life, disease and medicine [J].
Carmeliet, P .
NATURE, 2005, 438 (7070) :932-936