Active Gαi/o mutants accelerate breast tumor metastasis via the c-Src pathway

Abstract

AbstractConstitutively active mutations in the Gαi2and GαoAsubunits of heterotrimeric G proteins have been identified in several human cancers including breast cancer, but their functional significance in tumorigenesis and metastasis has not been well characterized. In this study, we show that expression of the constitutively active GαoAR243H and Gαi2R179C mutants alone was insufficient to induce mammary tumor formation in mice. However, in transgenic mouse models of breast cancer induced by Neu expression or PTEN loss, we found that the Gαi2R179C mutant enhanced spontaneous lung metastasis while having no effect on primary tumor initiation and growth. Additionally, we observed that ectopic expression of the GαoAR243H and Gαi2R179C mutants in tumor cells promote cell migrationin vitroas well as dissemination into multiple organsin vivoby activating c-Src signaling. Thus, our study uncovers a critical function of Gαi/osignaling in accelerating breast cancer metastasis via the c-Src pathway. This work is clinically significant, as it can potentially pave the way to personalized therapies for patients who present with active Gαi/omutations or elevated Gαi/osignaling by targeting c-Src to inhibit breast cancer metastasis.