Publication | Open Access
Phosphoinositide 3-Kinase p110β Activity: Key Role in Metabolism and Mammary Gland Cancer but Not Development
262
Citations
31
References
2008
Year
Breast OncologyKey RoleMetabolic RemodelingCancer BiologyInsulin SignalingMammary Gland DevelopmentTumor BiologySignaling PathwayReceptor Tyrosine KinaseCancer Cell BiologyMetabolic SignalingCancer MetabolismRadiation OncologyCell SignalingCancer ResearchMammary Gland CancerPharmacologyCell BiologyMild Insulin ResistanceProtein PhosphorylationSignal TransductionDiabetesMetabolic RegulationBreast CancerMouse MutantsGrowth RetardationMedicine
The phosphoinositide 3-kinase (PI3K) pathway crucially controls metabolism and cell growth. Although different PI3K catalytic subunits are known to play distinct roles, the specific in vivo function of p110beta (the product of the PIK3CB gene) is not clear. Here, we show that mouse mutants expressing a catalytically inactive PIK3CB(K805R) mutant survived to adulthood but showed growth retardation and developed mild insulin resistance with age. Pharmacological and genetic analyses of p110beta function revealed that p110beta catalytic activity is required for PI3K signaling downstream of heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors as well as to sustain long-term insulin signaling. In addition, PIK3CB(K805R) mice were protected in a model of ERBB2-driven tumor development. These findings indicate an unexpected role for p110beta catalytic activity in diabetes and cancer, opening potential avenues for therapeutic intervention.
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