Direct engagement of the PI3K pathway by mutant KIT dominates oncogenic signaling in gastrointestinal stromal tumor.

Abstract

Gastrointestinal stromal tumors (GISTs) predominantly harbor activating mutations in the receptor tyrosine kinase KIT. To genetically dissect in vivo the requirement of different signal transduction pathways emanating from KIT for tumorigenesis, the oncogenic <i>Kit</i>^{<i>V558Δ</i>} mutation was combined with point mutations abrogating specific phosphorylation sites on KIT. Compared with single-mutant <i>Kit</i>^{<i>V558Δ/+</i>} mice, double-mutant <i>Kit</i>^{<i>V558Δ;Y567F/Y567F</i>} knock-in mice lacking the SRC family kinase-binding site on KIT (pY567) exhibited attenuated MAPK signaling and tumor growth. Surprisingly, abrogation of the PI3K-binding site (pY719) in <i>Kit</i>^{<i>V558Δ;Y719F/Y719F</i>} mice prevented GIST development, although the interstitial cells of Cajal (ICC), the cells of origin of GIST, were normal. Pharmacologic inhibition of the PI3K pathway in tumor-bearing <i>Kit</i>^{<i>V558Δ/+</i>} mice with the dual PI3K/mTOR inhibitor voxtalisib, the pan-PI3K inhibitor pilaralisib, and the PI3K-alpha-restricted inhibitor alpelisib each diminished tumor proliferation. The addition of the MEK inhibitor PD-325901 or binimetinib further decreased downstream KIT signaling. Moreover, combining PI3K and MEK inhibition was effective against imatinib-resistant <i>Kit</i>^{<i>V558Δ;T669I/+</i>} tumors.