Small molecule αv integrin antagonists:: novel anticancer agents

被引:38
作者
Kerr, JS [1 ]
Slee, AM [1 ]
Mousa, SA [1 ]
机构
[1] Dupont Merck Pharmaceut Co, Expt Stn, Gen Pharmacol, Wilmington, DE 19880 USA
关键词
alpha(v); angiogenesis; cancer; integrin;
D O I
10.1517/13543784.9.6.1271
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The members of the integrin family are targets that potentially provide both therapeutic and diagnostic opportunities. Advances in the understanding of the signalling pathways, transcriptional regulation and the structure/function relationships of the adhesion molecules to extracellular matrix proteins have all contributed to these opportunities. The role of the integrins in pathological processes in both acute and chronic diseases, include ocular, cancer (solid rumours and metastasis), cardiovascular (stroke and heart failure) and inflammatory (rheumatoid arthritis) conditions. Various therapeutic candidates, including antibodies, cyclic peptides and peptidomimetics, have been identified. This review will focus on the key role of the alpha(v) integrin (alpha(v)beta(5) and alpha(v)beta(5)) in angiogenic processes in tumours, including its potential use in cancer diagnostics and therapy.
引用
收藏
页码:1271 / 1279
页数:9
相关论文
共 114 条
[1]   THE ALPHA-V-BETA-6 INTEGRIN PROMOTES PROLIFERATION OF COLON-CARCINOMA CELLS THROUGH A UNIQUE REGION OF THE BETA-6 CYTOPLASMIC DOMAIN [J].
AGREZ, M ;
CHEN, A ;
CONE, RI ;
PYTELA, R ;
SHEPPARD, D .
JOURNAL OF CELL BIOLOGY, 1994, 127 (02) :547-556
[2]  
ALBELDA SM, 1990, CANCER RES, V50, P6757
[3]   Angiogenesis at the interface between basic and clinical research [J].
Albini, A ;
Noonan, D ;
Santi, L .
INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 1999, 14 (04) :202-206
[4]   In vitro and in vivo effects of a cyclic peptide with affinity for the αvβ3 integrin in human melanoma cells [J].
Allman, R ;
Cowburn, P ;
Mason, M .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (03) :410-422
[5]  
Aplin AE, 1998, PHARMACOL REV, V50, P197
[6]   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
[7]   Type II' to type I beta-turn swap changes specificity for integrins [J].
Bach, AC ;
Espina, JR ;
Jackson, SA ;
Stouten, PFW ;
Duke, JL ;
Mousa, SA ;
DeGrado, WF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (01) :293-294
[8]   Extensive vasculogenesis, angiogenesis, and organogenesis precede lethality in mice lacking all αv integrins [J].
Bader, BL ;
Rayburn, H ;
Crowley, D ;
Hynes, RO .
CELL, 1998, 95 (04) :507-519
[9]   Disubstituted indazoles as potent antagonists of the integrin αvβ3 [J].
Batt, DG ;
Petraitis, JJ ;
Houghton, GC ;
Modi, DP ;
Cain, GA ;
Corjay, MH ;
Mousa, SA ;
Bouchard, PJ ;
Forsythe, MS ;
Harlow, PP ;
Barbera, FA ;
Spitz, SM ;
Wexler, RR ;
Jadhav, PK .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (01) :41-58
[10]  
BEVIGLIA L, 1995, ONCOL RES, V7, P7