MEK inhibition reduced vascular tumor growth and coagulopathy in a mouse model of hyperactive GNAQ


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MEK inhibition reduced vascular tumor growth and coagulopathy in a mouse model with hyperactive GNAQ Sandra Schrenk , Lindsay J Bischoff , Jillian Goines , Yuqi Cai , Shruti Vemaraju , Yoshinobu Odaka , Samantha R Good, Joseph S Palumbo, Sara Szabo 8, Damien Reynaud , Catherine D Van Raamsdonk , Richard A Lang , Elisa Boscolo Nat Commun. 2023 Apr 6;14(1):1929. doi: 10.1038/s41467-023-37516-7.



Activating non-inherited mutations in the guanine nucleotide-binding protein G(q) subunit alpha (GNAQ) gene family have been identified in childhood vascular tumors. Patients experience extensive disfigurement, chronic pain and severe complications including a potentially lethal coagulopathy termed Kasabach-Merritt phenomenon. Animal models for this class of vascular tumors do not exist. This has severely hindered the discovery of the molecular consequences of GNAQ mutations in the vasculature and, in turn, the preclinical development of effective targeted therapies. Here we report a mouse model expressing hyperactive mutant GNAQ in endothelial cells. Mutant mice develop vascular and coagulopathy phenotypes similar to those seen in patients. Mechanistically, by transcriptomic analysis we demonstrate increased mitogen activated protein kinase signaling in the mutant endothelial cells. Targeting of this pathway with Trametinib suppresses the tumor growth by reducing vascular cell proliferation and permeability. Trametinib also prevents the development of coagulopathy and improves mouse survival.



This work was supported by NIDDK U54 DK126108 at Cincinnati Children’s Hospital Medical Center Hematology Center Core.

Publication: 2023-10-13