4.8 Article

IL13 Receptor α2 Signaling Requires a Scaffold Protein, FAM120A, to Activate the FAK and PI3K Pathways in Colon Cancer Metastasis

Journal

CANCER RESEARCH
Volume 75, Issue 12, Pages 2434-2444

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-14-3650

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Funding

  1. contract to established research groups of the Asociacion Espanola Contra el Cancer (AECC)
  2. Comunidad de Madrid [S2011/BMD-2344/(Colomics2)]
  3. Juan de la Cierva fellowship
  4. Proteored-ISCIII contract
  5. Spanish Ministry of Economy and Competitiveness [BIO2012-31023]
  6. ProteoRed-ISCIII platform

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IL13 signaling through its receptor IL13R alpha 2 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. IL13R alpha 2-FAM120A coimmunoprecipitation experiments revealed further signaling network associations that could regulate the activity of IL13R alpha 2, 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. IL13R alpha 2-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 IL13-induced cell migration, invasion, and survival. Finally, antibody blockade of IL13R alpha 2 or FAM120A silencing precluded liver colonization in nude mice or metastasis. In conclusion, we identified FAM120A in the IL13/IL13R alpha 2 signaling pathway as a key mediator of invasion and liver metastasis in colon cancer. (C) 2015 AACR.

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