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磷酸肌醇 3-激酶/蛋白激酶 B 信号通路与肿瘤中 DNA 损伤反应和氧化应激的串扰。

Crosstalk between Phosphoinositide 3-kinase/Akt signaling pathway with DNA damage response and oxidative stress in cancer.

机构信息

Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Cancer & Immunology Research Center, Kurdistan University of Medical Sciences, Sanandaj, Iran.

出版信息

J Cell Biochem. 2019 Jun;120(6):10248-10272. doi: 10.1002/jcb.28309. Epub 2018 Dec 28.

Abstract

The phosphatidylinositol 3-kinases (PI3K)/Akt signaling pathway is one of the well-characterized and most important signaling pathways activated in response to DNA damage. This review discusses the most recent discoveries on the involvement of PI3K/Akt signaling pathway in cancer development, as well as stimulation of some important signaling networks involved in the maintenance of cellular homeostasis upon DNA damage, with an exploration of how PI3K/Akt signaling pathway contributes to the regulation of modulators and effectors underlying DNA damage response, the intricate, protein-based signal transduction network, which decides between cell cycle arrest, DNA repair, and apoptosis, the elimination of irreparably damaged cells to maintain homeostasis. The review continues by looking at the interplay between cell cycle checkpoints, checking the repair of damage inflicted to the DNA before entering DNA replication to facilitate DNA synthesis, and PI3K/Akt signaling pathway. We then investigate the challenges the cells overcome to ameliorate damages induced by oxidative activities, for example, the recruitment of many pathways and factors to maintain integrity and hemostasis. Finally, the review provides a discussion of how cells use the PI3K/Akt signaling pathway to regulate the balance between these networks.

摘要

磷脂酰肌醇 3-激酶(PI3K)/Akt 信号通路是一种已被充分研究的、最重要的信号通路之一,它在响应 DNA 损伤时被激活。本文讨论了 PI3K/Akt 信号通路在癌症发展中的最新发现,以及它在刺激参与维持细胞内稳态的一些重要信号网络方面的作用,这些信号网络涉及到 DNA 损伤后,PI3K/Akt 信号通路如何参与调节 DNA 损伤反应的调节剂和效应子,这个复杂的、基于蛋白质的信号转导网络决定了细胞周期停滞、DNA 修复和细胞凋亡之间的选择,从而消除无法修复的受损细胞以维持内稳态。本文接着探讨了细胞周期检查点之间的相互作用,细胞周期检查点在进入 DNA 复制之前检查 DNA 损伤的修复情况,以促进 DNA 合成,以及 PI3K/Akt 信号通路之间的相互作用。然后,我们研究了细胞克服氧化应激活动诱导损伤的挑战,例如,招募许多途径和因素来维持完整性和止血。最后,本文讨论了细胞如何利用 PI3K/Akt 信号通路来调节这些网络之间的平衡。

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