Author/Authors :
Kale، نويسنده , , Vijay Pralhad and Hengst، نويسنده , , Jeremy A. and Desai، نويسنده , , Dhimant H. and Dick، نويسنده , , Taryn E. and Choe، نويسنده , , Katherine N. and Colledge، نويسنده , , Ashley L. and Takahashi، نويسنده , , Yoshinori and Sung، نويسنده , , Shen-Shu and Amin، نويسنده , , Shantu G. and Yun، نويسنده , , Jong K.، نويسنده ,
Abstract :
Two structurally related protein kinase families, the Rho kinases (ROCK) and the myotonic dystrophy kinase-related Cdc42-binding kinases (MRCK) are required for migration and invasion of cancer cells. We hypothesized that simultaneous targeting of these two kinase families might represent a novel therapeutic strategy to block the migration and invasion of metastatic cancers. To this end, we developed DJ4 as a novel small molecule inhibitor of these kinases. DJ4 potently inhibited activities of ROCK and MRCK in an ATP competitive manner. In cellular functional assays, DJ4 treatment significantly blocked stress fiber formation and inhibited migration and invasion of multiple cancer cell lines in a concentration dependent manner. Our results strongly indicate that DJ4 may be further developed as a novel anti-metastatic chemotherapeutic agent for multiple cancers.
Keywords :
Stress fibers , cancer , rock , MRCK , Multikinase inhibitor , Migration
