In Vitro and In Vivo Efficacy on Retinal Neo-Vascularization of an Innovative Broad-Range Anti-Angiogenic Synthetic Peptide (Uparant)

被引:0
作者
Rusciano, D. [1 ]
Bagnoli, P. [2 ]
Presta, M. [3 ]
Semeraro, F. [4 ]
Dal Monte, M. [2 ]
Cammalleri, M. [2 ]
Rezzola, S. [3 ]
Belleri, M. [3 ]
Andre, H. [5 ]
Lista, L. [6 ]
De Rosa, M. [7 ]
Pavone, V [6 ]
机构
[1] Sooft Italia SpA, Dept Sci, I-00144 Rome, Italy
[2] Univ Pisa, Dept Biol, I-56100 Pisa, Italy
[3] Univ Brescia, Mol & Translat Med Dept, I-25121 Brescia, Italy
[4] Univ Hosp Brescia, Ophthalmol Unit, Brescia, Italy
[5] St Erik Eye Hosp, Karolinska Inst, Dept Clin Neurosci, Sect Ophthalmol & Vis, Stockholm, Sweden
[6] Univ Naples Federico II, Dept Chem Sci, Naples, Italy
[7] Seconda Univ Napoli, SUN, Dept Expt Med, Naples, Italy
来源
12TH ISOPT CLINICAL | 2016年
关键词
angiogenesis; retina; uparant; endothelial cells; VEGF;
D O I
暂无
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Pathologic blood neovessels growth in the macular region of the retina is responsible for several serious illnesses that can quickly lead to vision loss. Nowadays, some anti-angiogenic drugs for intravitreal use are present on the market, targeting the main angiogenic factor, VEGF. However, not all patients respond to anti-VEGF therapy (some 30% are classified as non-responders), and chronic suppression of VEGF (which appears to be also a neurotrophic factor) could exert some negative effects in the long run. We present here a new drug, a modified tetrapeptide, that works as an antagonist of the urokinase plasminogen activator cell receptor, that is able to inhibit the angiogenic response of endothelial cells to several different angiogenic and pro-inflammatory factors, since it blocks their motility and invasion independently from the trigger. We show evidence of its efficacy in widely known experimental model systems both in vitro and in vivo.
引用
收藏
页码:49 / 54
页数:6
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