Prostaglandin E2 activates cAMP response element-binding protein in glioma cells via a signaling pathway involving PKA-dependent inhibition of ERK

Prostaglandin E2 (PGE2) plays a critical role in influencing the biological behavior of tumor cells. We previously demonstrated that PGE2 stimulates human glioma cell growth via activation of protein kinase A (PKA) type II. This study was undertaken to further elucidate the intracellular pathways activated by PGE2 downstream to PKA. Stimulation of U87-MG glioma cells with PGE2 increased phosphorylation of the cyclic-AMP response element (CRE) binding protein CREB at Ser-133 and CREB-driven transcription in a dose- and time-dependent manner. Expression of dominant CREB constructs that interfere with CREB phosphorylation at Ser-133 or with its binding to the CRE site markedly decreased PGE2-induced CREB activation. Inhibition of PKA by H-89 or expression of a dominant negative PKA construct attenuated PGE2-induced CREB activation. Moreover, inhibition of PKA type II decreased PGE2-induced CREB-dependent transcription by 45% compared to vehicle-treated cells. To investigate the involvement of additional signaling pathways, U87-MG cells were pretreated with wortmannin or LY294002 to inhibit the PI3-kinase/AKT pathway. Both inhibitors had no effect on PGE2-induced CREB phosphorylation and transcriptional activity, suggesting that PGE2 activates CREB in a PI3-kinase/AKT independent manner. Challenge of U87-MG cells with PGE2, at concentrations that induced maximal CREB activation, or with forskolin inhibited extracellular signal-regulated kinase (ERK) phosphorylation. Pretreatment of U87-MG cells with the ERK inhibitor PD98059, accentuated ERK inhibition and increased CREB phosphorylation at Ser-133 and CREB-driven transcription stimulated by PGE2, suggesting that inhibition of ERK contributes to PGE2-induced CREB activation. Inhibition of ERK by PGE2 or by forskolin was rescued by treatment of cells with H-89 or by the dominant negative PKA construct. Moreover, PGE2 or forskolin inhibited phosphorylation of Raf-1 phosphorylation at Ser-338. Challenge of U87-MG cells with 11-deoxy-PGE1 increased CREB-driven transcription and stimulated cell growth, while other PGE2 analogues had no effect. Together our results reveal a novel signaling pathway whereby PGE2 signals through PKA to inhibit ERK and increase CREB transcriptional activity.