IL-13 receptor α2 signaling requires a scaffold protein, FAM120A, to activate the FAK and PI3K pathways in colon cancer metastasis.
By: Ruben A Bartolome, Irene García-Palmero, Sofia Torres, Maria Lopez-Lucendo, Irina V Balyasnikova, J Ignacio Casal

Functional Proteomics. Department of Cellular and Molecular Medicine, CENTRO DE INVESTIGACIONES BIOLOGICAS.
2015-4-22; doi: 10.1158/0008-5472.CAN-14-3650
Abstract

IL-13 signaling through its receptor IL13Rα2 plays a critical role in colon cancer invasion and liver metastasis, but the mechanistic features of this process are obscure. In this study, we identified a scaffold protein, FAM120A (C9ORF10), as a signaling partner in this process. FAM120A was overexpressed in human colon cancer cell lines and 55% of human colon cancer specimens. IL13Rα2-FAM120A co-immunoprecipitation experiments revealed further signaling network associations that could regulate the activity of IL13Rα2, including FAK, SRC, PI3K, G-protein coupled receptors and TRAIL receptors. In addition, FAM120A associated with kinesins and motor proteins involved in cargo movement along microtubules. IL13Rα2-triggered activation of the FAK and PI3K/AKT/mTOR pathways was mediated by FAM120A, which also recruited PI3K and functioned as a scaffold protein to enable phosphorylation and activation of PI3K by Src family kinases. FAM120A silencing abolished IL-13-induced cell migration, invasion and survival. Finally, antibody blockade of IL13Rα2 or FAM120A silencing precluded liver colonization in nude mice or metastasis. In conclusion, we identified FAM120A in the IL-13/IL13Rα2 signaling pathway as a key mediator of invasion and liver metastasis in colon cancer.



Copyright © 2015, American Association for Cancer Research.

PMID:25896327






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