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超越抗氧化剂:氧化还原途径如何塑造细胞信号传导和疾病结局

Beyond Antioxidants: How Redox Pathways Shape Cellular Signaling and Disease Outcomes.

作者信息

Alhaj Sulaiman Abdallah, Katanaev Vladimir L

机构信息

Translational Oncology Research Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University (HBKU), Qatar Foundation (QF), Doha P.O. Box 34110, Qatar.

Translational Research Centre in Oncohaematology, Department of Cell Physiology and Metabolism, Faculty of Medicine, University of Geneva, Rue Michel-Servet 1, CH-1211 Geneva, Switzerland.

出版信息

Antioxidants (Basel). 2025 Sep 22;14(9):1142. doi: 10.3390/antiox14091142.

Abstract

Cellular redox pathways are critical regulators of various biological processes, including the intricate modulation of intracellular signaling pathways. This review explores how major redox enzymes-such as catalase, superoxide dismutases, glutathione peroxidases, thioredoxins, and peroxiredoxins-interact with key cellular signaling pathways, including receptor tyrosine kinase, mTORC1/AMPK, Wnt/β-catenin, TGF-β/SMAD, NF-κB, Hedgehog, Notch, and GPCR signaling. By investigating mechanisms such as ROS-mediated activation, cysteine oxidation, spatial enzyme localization, and phosphatase regulation, we demonstrate the extensive influence of redox balance on cellular signaling dynamics. Understanding these redox-dependent interactions provides insights into pathophysiological conditions ranging from cancer to fibrosis, offering novel therapeutic opportunities.

摘要

细胞氧化还原途径是各种生物过程的关键调节因子,包括对细胞内信号通路的复杂调控。本综述探讨了主要的氧化还原酶,如过氧化氢酶、超氧化物歧化酶、谷胱甘肽过氧化物酶、硫氧还蛋白和过氧化物还原酶,如何与关键的细胞信号通路相互作用,包括受体酪氨酸激酶、mTORC1/AMPK、Wnt/β-连环蛋白、TGF-β/SMAD、NF-κB、Hedgehog、Notch和GPCR信号通路。通过研究ROS介导的激活、半胱氨酸氧化、酶的空间定位和磷酸酶调节等机制,我们证明了氧化还原平衡对细胞信号动力学的广泛影响。了解这些氧化还原依赖性相互作用有助于深入了解从癌症到纤维化等病理生理状况,提供新的治疗机会。

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