Feed-forward stimulation of CAMK2 by the oncogenic pseudokinase PEAK1 generates a therapeutically ‘actionable’ signalling axis in triple negative breast cancer
医学
作者
Xue Yang,Xiuquan Ma,David R. Croucher,Elizabeth V. Nguyen,Kimberley C. Clark,Changyuan Hu,Sharissa L. Latham,Tianyue Zhao,Charles Bayly-Jones,Viet Chi Bao Nguyen,Sung‐Young Shin,Lan K. Nguyen,Thomas R. Cotton,Anderly C. Chüeh,Terry C.C. Lim Kam Sian,Margaret M. Stratton,Andrew M. Ellisdon,Roger J. Daly
The PEAK family of pseudokinases, comprising PEAK1-3, are signalling scaffolds that play oncogenic roles in several poor prognosis human cancers, including triple negative breast cancer (TNBC). However, therapeutic targeting of pseudokinases is challenging due to their lack of catalytic activity. To address this, we screened for PEAK1 effectors by affinity purification and mass spectrometry, identifying calcium/calmodulin-dependent protein kinase 2 (CAMK2)D and CAMK2G. PEAK1 promoted CAMK2D/G activation in TNBC cells via a novel feed-forward mechanism involving PEAK1/PLCγ1/Ca