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It is known that amphibian oocytes undergo maturation through the formation and activation of maturation-promoting factor (MPF) in response to stimulation by the maturation-inducing hormone progesterone; however, the signal transduction pathway that links the hormonal stimulation on the oocyte surface to the activation of MPF in the oocyte cytoplasm remains a mystery. The aim of this study was to investigate whether the signal transduction mediated by phosphatidylinositol 3-kinase (P13K), protein kinase B (PKB), and glycogen synthase kinase 3β (GSK3β) is involved in progesterone-induced oocyte maturation in the Japanese brown frog, Rana japonica. Inhibitors of P13K, wortmannin and LY294002, inhibited progesterone-stimulated germinal vesicle breakdown (GVBD) only when the oocytes were treated at the initial phase of maturation, suggesting that P13K is involved in the progesterone-induced maturation of Rana oocytes. However, we also obtained results suggesting that PKB and GSK3β are not involved in Rana oocyte maturation. A constitutively active PKB expressed in the oocytes failed to induce GVBD in the absence of progesterone despite its high level of kinase activity. A Myc-tagged PKB expressed in the oocytes (used to monitor endogenous PKB activity) was not activated in the process of progesterone-induced oocyte maturation. Overexpression of GSK3β, which is reported to retard the progress of Xenopus oocyte maturation, had no effect on Rana oocyte maturation. On the basis of these results, we propose that P13K is involved in the initiation of Rana oocyte maturation, but that neither PKB nor GSK3β is a component of the P13K signal transduction pathway. [ABSTRACT FROM AUTHOR]

The PI3Kα inhibitor alpelisib achieved a 58.2% disease control rate in PIK3CA -altered solid tumors., (©2018 American Association for Cancer Research.)