Department of Pharmacological and Biomolecular Sciences "Rodolfo Paoletti", Università degli Studi di Milano, Milan, Italy.
Int J Biol Sci. 2024 May 27;20(8):3113-3125. doi: 10.7150/ijbs.89942. eCollection 2024.
Aberrant activation of the PI3K/Akt pathway commonly occurs in cancers and correlates with multiple aspects of malignant progression. In particular, recent evidence suggests that the PI3K/Akt signaling plays a fundamental role in promoting the so-called aerobic glycolysis or Warburg effect, by phosphorylating different nutrient transporters and metabolic enzymes, such as GLUT1, HK2, PFKB3/4 and PKM2, and by regulating various molecular networks and proteins, including mTORC1, GSK3, FOXO transcription factors, MYC and HIF-1α. This leads to a profound reprogramming of cancer metabolism, also impacting on pentose phosphate pathway, mitochondrial oxidative phosphorylation, de novo lipid synthesis and redox homeostasis and thereby allowing the fulfillment of both the catabolic and anabolic demands of tumor cells. The present review discusses the interactions between the PI3K/Akt cascade and its metabolic targets, focusing on their possible therapeutic implications.
PI3K/Akt 通路的异常激活在癌症中普遍存在,与恶性进展的多个方面相关。特别是,最近的证据表明,PI3K/Akt 信号通路通过磷酸化不同的营养转运体和代谢酶,如 GLUT1、HK2、PFKB3/4 和 PKM2,并通过调节包括 mTORC1、GSK3、FOXO 转录因子、MYC 和 HIF-1α 在内的各种分子网络和蛋白质,在促进所谓的有氧糖酵解或瓦博格效应方面起着至关重要的作用。这导致了癌症代谢的深刻重编程,也影响了磷酸戊糖途径、线粒体氧化磷酸化、从头脂质合成和氧化还原平衡,从而使肿瘤细胞的分解代谢和合成代谢需求都得到满足。本文讨论了 PI3K/Akt 级联与其代谢靶标的相互作用,重点讨论了它们可能的治疗意义。