%0 Journal Article
%T MERTK Inhibition as a Targeted Novel Cancer Therapy.
%A Tanim KM
%A Holtzhausen A
%A Thapa A
%A Huelse JM
%A Graham DK
%A Earp HS
%J Int J Mol Sci
%V 25
%N 14
%D 2024 Jul 12
%M 39062902
%F 6.208
%R 10.3390/ijms25147660
%X In this issue honoring the contributions of Greg Lemke, the Earp and Graham lab teams discuss several threads in the discovery, action, signaling, and translational/clinical potential of MERTK, originally called c-mer, a member of the TYRO3, AXL, and MERTK (TAM) family of receptor tyrosine kinases. The 30-year history of the TAM RTK family began slowly as all three members were orphan RTKs without known ligands and/or functions when discovered by three distinct alternate molecular cloning strategies in the pre-genome sequencing era. The pace of understanding their physiologic and pathophysiologic roles has accelerated over the last decade. The activation of ligands bridging externalized phosphatidylserine (PtdSer) has placed these RTKs in a myriad of processes including neurodevelopment, cancer, and autoimmunity. The field is ripe for further advancement and this article hopefully sets the stage for further understanding and therapeutic intervention. Our review will focus on progress made through the collaborations of the Earp and Graham labs over the past 30 years.