Focà Annalia, Sanguigno Luca, Focà Giuseppina, Strizzi Luigi, Iannitti Roberta, Palumbo Rosanna, Hendrix Mary J C, Leonardi Antonio, Ruvo Menotti, Sandomenico Annamaria
Institute of Biostructure and Bioimaging, National Research Council (IBB-CNR) and Centro Interuniversitario di Ricerca sui Peptidi Bioattivi (CIRPeB), Università degli Studi di Napoli "Federico II", Naples 80134, Italy.
Department of Pharmacy, Università degli Studi di Napoli "Federico II", Naples 80131, Italy.
Int J Mol Sci. 2015 Sep 7;16(9):21342-62. doi: 10.3390/ijms160921342.
Nodal is a potent embryonic morphogen belonging to the TGF-β 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.
Nodal是一种属于转化生长因子-β超家族的强效胚胎形态发生素。通常,在共受体Cripto-1存在的情况下,它还会与ALK4/ActRIIB受体复合物结合。Nodal的表达在生理上局限于胚胎组织和人类胚胎干细胞,在正常细胞中不存在,但在包括黑色素瘤、乳腺癌和结肠癌在内的几种人类癌症中重新出现。我们的目标是获得能够在主要CBR(Cripto结合区域)位点识别Nodal并阻断Cripto-1介导信号传导的单克隆抗体。为了实现这一目标,我们制备了针对hNodal(44-67)的抗体,并通过杂交瘤技术产生了单克隆抗体。我们选择了一种名为3D1的单克隆抗体,它与全长rhNodal强烈结合(解离常数为1.4 nM),并通过蛋白质印迹和荧光激活细胞分选分析在一组人类黑色素瘤细胞系中识别内源性蛋白。3D1抑制Nodal与Cripto-1的结合并阻断Smad2/3磷酸化。数据表明,抑制Nodal-Cripto-1轴是一种针对黑色素瘤的有效治疗方法,3D1是一种有前景且有趣的阻断Nodal-Cripto介导肿瘤发展的药物。这些发现增加了人们对Nodal作为诊断和预后标志物以及作为治疗干预潜在新靶点的兴趣。