PMID: 21499296

Phosphoproteomic mass spectrometry profiling links Src family kinases to escape from HER2 tyrosine kinase inhibition.

Abstract

Despite the initial effectiveness of the tyrosine kinase inhibitor lapatinib against HER2 gene-amplified breast cancers, most patients eventually relapse after treatment, implying that tumors acquire mechanisms of drug resistance. To discover these mechanisms, we generated six lapatinib-resistant

PTM Type Substrate Site PTM Enzyme Source
Phosphorylation iPTM:P04626 (ERBB2)
PRO
Y1248 RLIMS-P
Phosphorylation iPTM:P12931 (SRC)
PRO
Y216 RLIMS-P