肿瘤中的 mTORC1 与铁凋亡的关系

Huilin Liao, Yueqing Wang, Lili Zou, Yanmei Fan, Xinyue Wang, Xiancong Tu, Qiaobai Zhu, Jun Wang, Xiaowen Liu, Chuanjiang Dong
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引用次数: 0

摘要

铁凋亡是一种新型的程序性死亡,依赖于铁离子和氧化应激,细胞内主要是脂质过氧化。mTOR 始终在肿瘤中过表达,控制着细胞的生长和代谢活动,在自噬和铁变性中都扮演着重要角色。有趣的是,自噬的选择性类型在促进铁突变中起着重要作用,而铁突变与 mTOR 和一些代谢途径(尤其是铁和氨基酸)有关。在本文中,我们列举了铁突变与 mTOR 信号通路的主要联系机制,并进一步总结了目前通过这些途径靶向铁突变的化合物。越来越多的实验证据表明,以 mTOR 和铁突变为靶点可能会对许多肿瘤产生有效的影响,而了解 mTOR 与铁突变之间的联系机制可能会为肿瘤治疗提供一种潜在的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Relationship of mTORC1 and ferroptosis in tumors

Ferroptosis is a novel form of programmed death, dependent on iron ions and oxidative stress, with a predominant intracellular form of lipid peroxidation. In recent years, ferroptosis has gained more and more interest of people in the treatment mechanism of targeted tumors. mTOR, always overexpressed in the tumor, and controlling cell growth and metabolic activities, has an important role in both autophagy and ferroptosis. Interestingly, the selective types of autophay plays an important role in promoting ferroptosis, which is related to mTOR and some metabolic pathways (especially in iron and amino acids). In this paper, we list the main mechanisms linking ferroptosis with mTOR signaling pathway and further summarize the current compounds targeting ferroptosis in these ways. There are growing experimental evidences that targeting mTOR and ferroptosis may have effective impact in many tumors, and understanding the mechanisms linking mTOR to ferroptosis could provide a potential therapeutic approach for tumor treatment.

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