In GH3 pituitary tumor cells or primary cultures of anterior pituitary cells from rat, the PrRP receptor appears to signal via multiple kinase pathways including mitogen-activated protein kinase (MAPK), Jun N-terminal kinase (JNK), and serine/threonine kinase (Akt/protein kinase B) to the PRL promoter; these pathways require an Ets transcription factor (26, 27). Here, AKT1 is linked to pituitary tumor.