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New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding

Authors :
Giuseppina Focà
Antonio Leonardi
Mary J.C. Hendrix
Menotti Ruvo
Annalia Focà
Rosanna Palumbo
Roberta Iannitti
Annamaria Sandomenico
Luigi Strizzi
Luca Sanguigno
Focà, Annalia
Sanguigno, Luca
Focà, Giuseppina
Strizzi, Luigi
Iannitti, Roberta
Palumbo, Rosanna
Hendrix, Mary J. C.
Leonardi, Antonio
Ruvo, Menotti
Sandomenico, Annamaria
Source :
International Journal of Molecular Sciences, Volume 16, Issue 9, Pages 21342-21362, International Journal of Molecular Sciences, Vol 16, Iss 9, Pp 21342-21362 (2015), International journal of molecular sciences (Online) 16 (2015): 21342–62. doi:10.3390/ijms160921342, info:cnr-pdr/source/autori:Foca, Annalia; Sanguigno, Luca; Foca, Giuseppina; Strizzi, Luigi; Iannitti, Roberta; Palumbo, Rosanna; Hendrix, Mary J C; Leonardi, Antonio; Ruvo, Menotti; Sandomenico, Annamaria/titolo:New Anti-Nodal Monoclonal Antibodies Targeting the Nodal Pre-Helix Loop Involved in Cripto-1 Binding./doi:10.3390%2Fijms160921342/rivista:International journal of molecular sciences (Online)/anno:2015/pagina_da:21342/pagina_a:62/intervallo_pagine:21342–62/volume:16
Publication Year :
2015
Publisher :
MDPI AG, 2015.

Abstract

Nodal is a potent embryonic morphogen belonging to the TGF-beta superfamily. Typically, it also binds to the ALK4/ActRIIB receptor complex in the presence of the co-receptor Cripto-1. Nodal expression is physiologically restricted to embryonic tissues and human embryonic stem cells, is absent in normal cells but re-emerges in several human cancers, including melanoma, breast, and colon cancer. Our aim was to obtain mAbs able to recognize Nodal on a major CBR (Cripto-Binding-Region) site and to block the Cripto-1-mediated signalling. To achieve this, antibodies were raised against hNodal(44-67) and mAbs generated by the hybridoma technology. We have selected one mAb, named 3D1, which strongly associates with full-length rhNodal (KD 1.4 nM) and recognizes the endogenous protein in a panel of human melanoma cell lines by western blot and FACS analyses. 3D1 inhibits the Nodal-Cripto-1 binding and blocks Smad2/3 phosphorylation. Data suggest that inhibition of the Nodal-Cripto-1 axis is a valid therapeutic approach against melanoma and 3D1 is a promising and interesting agent for blocking Nodal-Cripto mediated tumor development. These findings increase the interest for Nodal as both a diagnostic and prognostic marker and as a potential new target for therapeutic intervention.

Details

ISSN :
14220067
Volume :
16
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences
Accession number :
edsair.doi.dedup.....9a3aa1f8b6a4b3a935c2e53b5eb606ee