Tensin-4-Dependent MET Stabilization Is Essential for Survival and Proliferation in Carcinoma Cells

(Developmental Cell 26, 393–404; August 26, 2013) Following the online publication of this paper, the authors noticed that the control loading panel for total MET levels in the nontreated A549-GFP cells in Figure 5A was incorrectly inserted. The mistake has been amended online and the correct western blot panel has been inserted in the final version of Figure 5, shown below. The authors apologize for any possible confusion this error might have caused. Tensin-4-Dependent MET Stabilization Is Essential for Survival and Proliferation in Carcinoma CellsMuharram et al.Developmental CellMay 8, 2014In BriefMuharram et al. demonstrate that a direct interaction between MET and TNS4, a recently characterized oncogene, inhibits MET trafficking and induces MET stability, cell proliferation, migration, and survival of MET-addicted carcinomas in vivo. A significant correlation among MET-TNS4 levels in human carcinomas suggests clinical relevance of TNS4-dependent MET stabilization.