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穿梭于氧化还原景观:活性氧在细胞周期调控中的作用。

Navigating the redox landscape: reactive oxygen species in regulation of cell cycle.

机构信息

Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

Department of Physiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.

出版信息

Redox Rep. 2024 Dec;29(1):2371173. doi: 10.1080/13510002.2024.2371173. Epub 2024 Jul 7.

DOI:10.1080/13510002.2024.2371173
PMID:38972297
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11637001/
Abstract

To advance our knowledge of disease mechanisms and therapeutic options, understanding cell cycle regulation is critical. Recent research has highlighted the importance of reactive oxygen species (ROS) in cell cycle regulation. Although excessive ROS levels can lead to age-related pathologies, ROS also play an essential role in normal cellular functions. Many cell cycle regulatory proteins are affected by their redox status, but the precise mechanisms and conditions under which ROS promote or inhibit cell proliferation are not fully understood. This review presents data from the scientific literature and publicly available databases on changes in redox state during the cell cycle and their effects on key regulatory proteins. We identified redox-sensitive targets within the cell cycle machinery and analysed different effects of ROS (type, concentration, duration of exposure) on cell cycle phases. For example, moderate levels of ROS can promote cell proliferation by activating signalling pathways involved in cell cycle progression, whereas excessive ROS levels can induce DNA damage and trigger cell cycle arrest or cell death. Our findings encourage future research focused on identifying redox-sensitive targets in the cell cycle machinery, potentially leading to new treatments for diseases with dysregulated cell proliferation.

摘要

为了深入了解疾病机制和治疗选择,理解细胞周期调控至关重要。最近的研究强调了活性氧(ROS)在细胞周期调控中的重要性。虽然过量的 ROS 水平会导致与年龄相关的病理,但 ROS 在正常细胞功能中也起着重要作用。许多细胞周期调节蛋白的活性受其氧化还原状态的影响,但 ROS 促进或抑制细胞增殖的确切机制和条件尚不完全清楚。本综述介绍了来自科学文献和公开数据库的数据,这些数据涉及细胞周期过程中氧化还原状态的变化及其对关键调节蛋白的影响。我们鉴定了细胞周期机制中的氧化还原敏感靶点,并分析了 ROS(类型、浓度、暴露持续时间)对细胞周期各阶段的不同影响。例如,适度的 ROS 水平可以通过激活参与细胞周期进程的信号通路来促进细胞增殖,而过量的 ROS 水平会导致 DNA 损伤,并引发细胞周期停滞或细胞死亡。我们的研究结果鼓励未来的研究集中在鉴定细胞周期机制中的氧化还原敏感靶点,这可能为细胞增殖失调的疾病提供新的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/3ffc46e0213f/YRER_A_2371173_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/ced9c1a7f000/YRER_A_2371173_F0001_OC.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/1d41f3bebf4e/YRER_A_2371173_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/3ffc46e0213f/YRER_A_2371173_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/ced9c1a7f000/YRER_A_2371173_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/fee69feb3d26/YRER_A_2371173_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/1d41f3bebf4e/YRER_A_2371173_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbee/11637001/3ffc46e0213f/YRER_A_2371173_F0004_OC.jpg

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