医学研究与教育 ›› 2026, Vol. 43 ›› Issue (5): 1-11.DOI: 10.3969/j.issn.1674-490X.2026.05.001

• 基础医学 •    

核苷酸代谢调控及其在肿瘤中的重编程与靶向治疗

李晨阳,郄楚楚,李文娟   

  1. 1.河北大学基础医学院, 河北 保定 071000;
    2. 河北省炎性自身免疫性疾病发病机制及防治重点实验室, 河北 保定 071000
  • 收稿日期:2026-05-18 发布日期:2026-10-21
  • 通讯作者: 李文娟(1977—),女,甘肃静宁人,教授,博士,硕士生导师,主要从事肿瘤代谢的研究。E-mail: liwenjuan@hbu.edu.cn
  • 作者简介:李晨阳(1999—),女,河北保定人,在读硕士,主要从事肿瘤代谢及化学预防的研究。 E-mail: 15127232590@163.com

Nucleotide metabolism regulation and its reprogramming in tumors with targeted therapeutic strategies

Li Chenyang, Ke Chuchu, Li Wenjuan   

  1. 1.School of Basic Medical Sciences, Hebei University, Baoding 071000, China; 2. Key Laboratory of Pathogenesis Mechanism and Control of Inflammatory Autoimmune Diseases of Hebei Province, Baoding 071000, China
  • Received:2026-05-18 Published:2026-10-21

摘要: 核苷酸代谢通过从头合成与补救途径维持细胞内dNTP平衡与核苷酸池稳态,为DNA复制及RNA转录提供前体,同时参与能量代谢调控与表观修饰底物供给。肿瘤中该代谢网络发生重编程,受癌基因信号及肿瘤微环境的多重调控,驱动异常增殖并维持基因组稳定性。然而,核苷酸代谢关键酶的非经典功能与通路动态调控机制仍未充分阐明。临床应用中,现有靶向药物面临肿瘤特异性不足、毒副作用显著及易耐药等瓶颈。系统阐述肿瘤核苷酸代谢的调控机制及其在治疗耐药中的作用,以期为肿瘤精准靶向治疗提供新思路和理论依据。

关键词: 核苷酸代谢, 关键酶, 代谢重编程, 靶向治疗

Abstract: Nucleotide metabolism maintains intracellular dNTP balance and nucleotide pool homeostasis through de novo synthesis and salvage pathways, providing precursors for DNA replication and RNA transcription while also contributing to energy metabolism regulation and supplying substrates for epigenetic modifications. In tumors, this metabolic network undergoes reprogramming, driven by oncogenic signals and tumor microenvironment, which fuels abnormal proliferation and maintains genomic stability. However, the non-classical functions of key enzymes in nucleotide metabolism and the dynamic regulatory mechanisms of these pathways remain poorly understood. Clinically, available targeted therapies face significant bottlenecks, including insufficient tumor specificity, marked toxic side effects, and susceptibility to drug resistance. This review systematically elaborates on the regulatory mechanisms of tumor nucleotide metabolism, and its role in therapeutic resistance, aiming to provide new insights and a theoretical basis for precision targeted therapy of tumors.

Key words: nucleotide metabolism, key enzymes, metabolic reprogramming, targeted therapy

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