Discovery of a Novel ERK Inhibitor with Activity in Models of Acquired Resistance to BRAF and MEK Inhibitors
Excerpt:
In addition, expression of MEK1F129L (allosteric binding site mutant with enhanced activity; refs. 17, 21) or MEK1DD (constitutively active mutant with aspartic acid replacement of activating loop serine residues; ref. 17) all mediated resistance to PLX4032 (Supplementary Fig. S8)