Peptide-based molecules in angiogenesis

被引:82
作者
D'Andrea, LD
Del Gatto, A
Pedone, C
Benedetti, E
机构
[1] CNR, Inst Biostruct & Bioimaging, I-80134 Naples, Italy
[2] Univ Naples Federico II, CIRPEB, Dept Biol Sci, I-80134 Naples, Italy
关键词
angiogenesis; cancer; integrins; ischemia; peptide; vascular endothelial growth factor;
D O I
10.1111/j.1747-0285.2006.00356.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Angiogenesis refers to the process of remodeling the vascular tissue characterized by the branching out of a new blood vessel from a pre-existing vessel. Angiogenesis is particularly active during embryogenesis, while during adult life it is quiescent and limited to particular physiologic phenomena. Recently, the study of molecular mechanisms of angiogenesis has stirred renewed interest due to the recognition of the role played by angiogenesis in several pathologies of significant medical impact, such as cancer and cardiovascular disease, and due to the pharmacologic interest rising from the possibility of modulating these phenomena. Antibodies, peptides and small molecules targeting active endothelial cells represent an innovative tool in therapeutic and diagnostic fields. In this study, we reviewed the literature of peptide and peptidomimetics in angiogenesis and their potential applications. Two specific protein systems, namely the vascular endothelial growth factor and its receptor and integrins, will be discussed in detail.
引用
收藏
页码:115 / 126
页数:12
相关论文
共 122 条
[1]   Vascular endothelial growth factor stimulates tyrosine phosphorylation and recruitment to new focal adhesions of focal adhesion kinase and paxillin in endothelial cells [J].
Abedi, H ;
Zachary, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (24) :15442-15451
[2]   INTEGRINS AND OTHER CELL-ADHESION MOLECULES [J].
ALBELDA, SM ;
BUCK, CA .
FASEB JOURNAL, 1990, 4 (11) :2868-2880
[3]   The angiogenesis induced by HIV-1 Tat protein is mediated by the Flk-1/KDR receptor on vascular endothelial cells [J].
Albini, A ;
Soldi, R ;
Giunciuglio, D ;
Giraudo, E ;
Benelli, R ;
Primo, L ;
Noonan, D ;
Salio, M ;
Camussi, G ;
Rockl, W ;
Bussolino, F .
NATURE MEDICINE, 1996, 2 (12) :1371-1375
[4]   Suppression of tumor growth and metastasis by a vegfr-1 antagonizing peptide identified from a phage display library [J].
An, P ;
Lei, HT ;
Zhang, JZ ;
Song, SM ;
He, LW ;
Jin, GL ;
Liu, XY ;
Wu, J ;
Meng, L ;
Liu, MS ;
Shou, CC .
INTERNATIONAL JOURNAL OF CANCER, 2004, 111 (02) :165-173
[5]   Suppression of tumor growth by novel peptides homing to tumor-derived new blood vessels [J].
Asai, T ;
Nagatsuka, M ;
Kuromi, K ;
Yamakawa, S ;
Kurohane, K ;
Ogino, K ;
Tanaka, M ;
Taki, T ;
Oku, N .
FEBS LETTERS, 2002, 510 (03) :206-210
[6]   ARG-GLY-ASP CONSTRAINED WITHIN CYCLIC PENTAPEPTIDES - STRONG AND SELECTIVE INHIBITORS OF CELL-ADHESION TO VITRONECTIN AND LAMININ FRAGMENT-P1 [J].
AUMAILLEY, M ;
GURRATH, M ;
MULLER, G ;
CALVETE, J ;
TIMPL, R ;
KESSLER, H .
FEBS LETTERS, 1991, 291 (01) :50-54
[7]   Role of PIGF in the intra- and intermolecular cross talk between the VEGF receptors Flt1 and Flk1 [J].
Autiero, M ;
Waltenberger, J ;
Communi, D ;
Kranz, A ;
Moons, L ;
Lambrechts, D ;
Kroll, J ;
Plaisance, S ;
De Mol, M ;
Bono, F ;
Kliche, S ;
Fellbrich, G ;
Ballmer-Hofer, K ;
Maglione, D ;
Mayr-Beyrle, U ;
Dewerchin, M ;
Dombrowski, S ;
Stanimirovic, D ;
Van Hummelen, P ;
Dehio, C ;
Hicklin, DJ ;
Persico, G ;
Herbert, JM ;
Communi, D ;
Shibuya, M ;
Collen, D ;
Conway, EM ;
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (07) :936-943
[8]   Arginine-rich anti-vascular endothelial growth factor peptides inhibit tumor growth and metastasis by blocking angiogenesis [J].
Bae, DG ;
Gho, YS ;
Yoon, WH ;
Chae, CB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (18) :13588-13596
[9]   Potent integrin antagonists from a small library of RGD-including cyclic pseudopeptides [J].
Belvisi, L ;
Bernardi, A ;
Checchia, A ;
Manzoni, L ;
Potenza, D ;
Scolastico, C ;
Castorina, M ;
Cupelli, A ;
Giannini, G ;
Carminati, P ;
Pisano, C .
ORGANIC LETTERS, 2001, 3 (07) :1001-1004
[10]   Tumorigenesis and the angiogenic switch [J].
Bergers, G ;
Benjamin, LE .
NATURE REVIEWS CANCER, 2003, 3 (06) :401-410