Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Naunyn Schmiedebergs Arch Pharmacol. 2024 May;397(5):2531-2549. doi: 10.1007/s00210-023-02782-1. Epub 2023 Oct 25.
The control of biological cell death is essential for the body's appropriate growth. The resistance of cells to the apoptotic process presents a new difficulty in the treatment of cancer. To combat cancer cells, researchers are working to find new apoptotic pathways and components to activate. One of the processes of regulated cell death (RCD) is referred to as ferroptosis marked by a decline in the activity of lipid glutathione peroxidase 4 (GPX4) after the buildup of reactive oxygen species (ROS). Since lipid peroxidation is a crucial component of ferroptosis and is required for its start, numerous medicines have been studied, particularly for the treatment of cancer. In this context, autophagy is an additional form of RCD that can govern ferroptosis through shared signaling pathways/factors involved in both mechanisms. In this review, we will explore the molecular mechanisms underlying ferroptosis and its association with autophagy, to gain fresh insights into their interplay in cancer advancement, and the potential of natural products for its treatment.
生物细胞死亡的控制对于身体的正常生长至关重要。细胞对凋亡过程的抵抗给癌症的治疗带来了新的困难。为了对抗癌细胞,研究人员正在努力寻找新的凋亡途径和组件来激活。细胞程序性死亡(RCD)的一个过程被称为铁死亡,其特征是在活性氧(ROS)积累后脂质谷胱甘肽过氧化物酶 4(GPX4)的活性下降。由于脂质过氧化是铁死亡的关键组成部分,并且是其启动所必需的,因此已经研究了许多药物,特别是用于癌症的治疗。在这种情况下,自噬是另一种 RCD 形式,它可以通过参与这两种机制的共享信号通路/因子来控制铁死亡。在这篇综述中,我们将探讨铁死亡的分子机制及其与自噬的关联,以深入了解它们在癌症进展中的相互作用以及天然产物在其治疗中的潜力。