Targeting nucleotide metabolism: a promising approach to enhance cancer immunotherapy

被引:89
|
作者
Wu, Huai-liang [1 ]
Gong, Yue [1 ]
Ji, Peng [1 ]
Xie, Yi-fan [1 ]
Jiang, Yi-Zhou [1 ]
Liu, Guang-yu [1 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Key Lab Breast Canc Shanghai, Dept Breast Surg,Dept Oncol, 270 Dongan Rd, Shanghai 200032, Peoples R China
关键词
INOSINE MONOPHOSPHATE DEHYDROGENASE; PURINE NUCLEOSIDE PHOSPHORYLASE; ACUTE LYMPHOBLASTIC-LEUKEMIA; ACUTE MYELOID-LEUKEMIA; I CLINICAL-TRIAL; CELL LUNG-CANCER; DIHYDROPYRIMIDINE DEHYDROGENASE; OPEN-LABEL; ADJUVANT CHEMOTHERAPY; T-CELLS;
D O I
10.1186/s13045-022-01263-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeting nucleotide metabolism can not only inhibit tumor initiation and progression but also exert serious side effects. With in-depth studies of nucleotide metabolism, our understanding of nucleotide metabolism in tumors has revealed their non-proliferative effects on immune escape, indicating the potential effectiveness of nucleotide antimetabolites for enhancing immunotherapy. A growing body of evidence now supports the concept that targeting nucleotide metabolism can increase the antitumor immune response by (1) activating host immune systems via maintaining the concentrations of several important metabolites, such as adenosine and ATP, (2) promoting immunogenicity caused by increased mutability and genomic instability by disrupting the purine and pyrimidine pool, and (3) releasing nucleoside analogs via microbes to regulate immunity. Therapeutic approaches targeting nucleotide metabolism combined with immunotherapy have achieved exciting success in preclinical animal models. Here, we review how dysregulated nucleotide metabolism can promote tumor growth and interact with the host immune system, and we provide future insights into targeting nucleotide metabolism for immunotherapeutic treatment of various malignancies.
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页数:21
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