Department of Basic Medical Sciences, School of Medicine, Tsinghua University, Beijing, China.
Department of Basic Medical Sciences, School of Medicine, Tsinghua University, Beijing, China; Tsinghua-Peking Center for Life Sciences, Beijing, China.
Trends Endocrinol Metab. 2024 May;35(5):385-399. doi: 10.1016/j.tem.2023.12.010. Epub 2024 Jan 22.
The intracellular metabolic network comprises a variety of reduction-oxidation (redox) reactions that occur in a temporally and spatially distinct manner. In order to coordinate these redox processes, mammalian cells utilize a collection of electron-carrying molecules common to many redox reactions, including NAD, NADP, coenzyme Q (CoQ), and glutathione (GSH). This review considers the metabolic basis of redox regulation in the context of cell proliferation by analyzing how cells acquire and utilize electron carriers to maintain directional carbon flux, sustain reductive biosynthesis, and support antioxidant defense. Elucidating the redox requirement during cell proliferation can advance the understanding of human diseases such as cancer, and reveal effective therapeutic opportunities in the clinic.
细胞内代谢网络包含多种氧化还原(redox)反应,这些反应以时间和空间上独特的方式发生。为了协调这些氧化还原过程,哺乳动物细胞利用了许多氧化还原反应共有的一组电子载体分子,包括 NAD、NADP、辅酶 Q(CoQ)和谷胱甘肽(GSH)。本综述通过分析细胞如何获取和利用电子载体来维持定向碳通量、支持还原性生物合成以及支持抗氧化防御,从细胞增殖的角度考虑了氧化还原调节的代谢基础。阐明细胞增殖过程中的氧化还原需求可以促进对癌症等人类疾病的理解,并揭示临床治疗的有效机会。