Lyu Siying, Gildor Nina, Zhang Qing, Liao Chengheng
Department of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX, 75390, USA.
Sci China Life Sci. 2025 Nov;68(11):3281-3302. doi: 10.1007/s11427-025-2979-3. Epub 2025 Jul 25.
Metabolic reprogramming is a hallmark of cancer, playing a critical role in tumorigenesis by supporting cancer cell survival, proliferation, metastasis, and immune evasion. Oncogenic signaling pathways regulate key metabolic processes by orchestrating gene expression and enhancing metabolic enzyme activity, ensuring cancer cells meet their bioenergetic and biosynthetic demands. Here, we highlight the roles of major oncogenic metabolic signaling pathways, including phosphoinositide 3-kinase (PI3K)/AKT, Myc, p53, and hypoxia-inducible factor (HIF), in driving metabolic rewiring. We provide a conceptual framework to understand why metabolic reprogramming occurs in tumor cells, how metabolic alterations contribute to tumorigenesis, metastasis, and immune evasion, and the therapeutic implications of targeting these metabolic vulnerabilities in cancer.
代谢重编程是癌症的一个标志,通过支持癌细胞的存活、增殖、转移和免疫逃逸在肿瘤发生过程中发挥关键作用。致癌信号通路通过协调基因表达和增强代谢酶活性来调节关键代谢过程,确保癌细胞满足其生物能量和生物合成需求。在这里,我们强调主要致癌代谢信号通路的作用,包括磷酸肌醇3激酶(PI3K)/AKT、Myc、p53和缺氧诱导因子(HIF),在驱动代谢重排方面的作用。我们提供了一个概念框架,以理解为什么肿瘤细胞会发生代谢重编程,代谢改变如何促进肿瘤发生、转移和免疫逃逸,以及针对癌症中这些代谢弱点进行治疗的意义。