| Literature DB >> 33724150 |
Andrea A Villanueva1, Pilar Sanchez-Gomez2, Ernesto Muñoz-Palma1, Sofía Puvogel1, Bárbara S Casas1, Cecilia Arriagada3, Isaac Peña-Villalobos1, Pablo Lois4, Manuel Ramírez Orellana4, Fabiana Lubieniecki5, Fernando Casco Claro6, Iván Gallegos7, Javier García-Castro8, Vicente A Torres3, Verónica Palma1.
Abstract
Neuroblastoma is a highly metastatic tumor that emerges from neural crest cell progenitors. Focal Adhesion Kinase (FAK) is a regulator of cell migration that binds to the receptor Neogenin-1 and is upregulated in neuroblastoma. Here, we show that Netrin-1 ligand binding to Neogenin-1 leads to FAK autophosphorylation and integrin β1 activation in a FAK dependent manner, thus promoting neuroblastoma cell migration. Moreover, Neogenin-1, which was detected in all tumor stages and was required for neuroblastoma cell migration, was found in a complex with integrin β1, FAK, and Netrin-1. Importantly, Neogenin-1 promoted neuroblastoma metastases in an immunodeficient mouse model. Taken together, these data show that Neogenin-1 is a metastasis-promoting protein that associates with FAK, activates integrin β1 and promotes neuroblastoma cell migration.Entities:
Keywords: FAK; cell migration; Neogenin-1; Netrin-1; integrin-β1 activation; metastasis; neuroblastoma
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Year: 2021 PMID: 33724150 PMCID: PMC7971226 DOI: 10.1080/19336918.2021.1892397
Source DB: PubMed Journal: Cell Adh Migr ISSN: 1933-6918 Impact factor: 3.405