Abstract
While growth factor-driven dimerization of receptor tyrosine kinases (RTKs) is a simple and intuitive mechanism of activating RTKs, K.-I. Arimoto et al. (Mol. Cell. Biol. 34:3843-3854, 2014, doi:10.1128/MCB.00758-14) describe a novel means of promoting the activity of RTKs. Namely, plakophilin-2 (PKP2) associates with the epidermal growth factor receptor (EGFR) and enhances its ligand-dependent and ligand-independent activity. This discovery suggests that antagonizing PKP2 may be a new therapeutic opportunity to combat tumors in which activation of EGFR contributes to pathogenesis.
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CITATION STYLE
Kazlauskas, A. (2014). Plakophilin-2 Promotes Activation of Epidermal Growth Factor Receptor. Molecular and Cellular Biology, 34(20), 3778–3779. https://doi.org/10.1128/mcb.00968-14
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