A novel human fibronectin cryptic sequence unmasked by the insertion of the angiogenesis-associated extra type III domain B

被引:25
作者
Balza, Enrica [2 ]
Sassi, Francesca [2 ]
Ventura, Elisa [1 ]
Parodi, Arianna [1 ,3 ]
Fossati, Sara [1 ,3 ]
Blalock, William [1 ,3 ]
Carnemolla, Barbara [1 ,2 ,3 ,4 ]
Castellani, Patrizia [2 ]
Zardi, Luciano [1 ,3 ]
Borsi, Laura [2 ]
机构
[1] Ctr Biotecnol Avanzate, Lab Recombinant Therapeut Prot, I-16132 Genoa, Italy
[2] Ist Nazl Ric Canc, Cell Biol Lab, I-16132 Genoa, Italy
[3] Ist Giannina Gaslini, Unit Innovat Therapies, I-16148 Genoa, Italy
[4] Ist Nazl Ric Canc, Immunol Lab, I-16132 Genoa, Italy
关键词
oncofetal fibronectin; angiogenesis; tumor targeting; monoclonal antibodies; cryptic epitopes; PRE-MESSENGER-RNA; ED-B; ONCOFETAL FIBRONECTIN; MONOCLONAL-ANTIBODIES; TARGETED DELIVERY; TENASCIN ISOFORMS; SPLICING PATTERN; UTEROGLOBIN; EXPRESSION; MARKER;
D O I
10.1002/ijc.24473
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The angiogenesis-associated extra-domain B (EDB) of fibronectin (FN) is a complete type III repeat of 91 amino acids. Its expression is modulated by the alternative splicing pattern of the FN premRNA. FN containing the EDB (B-FN) is undetectable in tissues of healthy adults, with rare exceptions such as the female reproductive system where tissue remodeling and angiogenesis are recurrent physiological processes. On the contrary, B-FN is expressed at high levels in neoplastic tissues and during angiogenesis; consequently, it is considered an excellent marker of angiogenesis. Here, we report on a novel FN cryptic sequence, localized on the FN type III repeat 8 (immediately downstream of the EDB) that is unmasked by the insertion of the EDB. This sequence is specifically recognized by the high-affinity monoclonal antibody, C6, that selectively recognizes B-FN by means of ELISA, immunohistochemical and Western blot assays. The variable regions of C6 were cloned and a divalent covalently linked mini-antibody was generated. Biodistribution studies using the radioiodinated C6 mini-antibody on tumor-bearing mice demonstrated an efficient tumor targeting. This antibody represents a new tool for the study of the potential biological functions of hindered sequences that the inclusion of the EDB renders accessible, and likewise makes its epitope an additional angiogenesis target. (C) 2009 UICC
引用
收藏
页码:751 / 758
页数:8
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