Polyamine metabolism and anti-tumor immunity

被引:3
作者
Wu, Jing-Yi [1 ]
Zeng, Yan [1 ]
You, Yu-Yang [1 ]
Chen, Qi-Yue [2 ]
机构
[1] Fujian Med Univ, Fuzhou, Fujian, Peoples R China
[2] Fujian Med Univ, Dept Gastr Surg, Union Hosp, Fuzhou, Peoples R China
关键词
polyamine; tumorigenesis; polyamine combination therapeutic strategies; metabolism; tumor microenvironment; CELLS; SPERMIDINE; EXPRESSION; TRANSPORT; PATHWAY; INHIBITION; MECHANISMS; HYPOXIA; MYC;
D O I
10.3389/fimmu.2025.1529337
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Growing attention has been directed toward the critical role of polyamines in the tumor microenvironment and immune regulation. Polyamines, primarily comprising putrescine, spermidine, and spermine, are tightly regulated through coordinated biosynthesis, catabolism, and transport, with distinct metabolic patterns between normal and cancerous tissues. Emerging evidence highlights the pivotal role of polyamine metabolism in tumor initiation, progression, and metastasis. This review aims to elucidate the differences in polyamine biosynthesis, transport, and catabolism between normal and cancerous tissues, as well as the associated alterations in tumor epigenetic modifications and resistance to immune checkpoint blockade driven by polyamine metabolism. Polyamine metabolism influences both tumor cells and the tumor microenvironment by modulating immune cell phenotypes-shifting them towards either tumor suppression or immune evasion within the tumor immune microenvironment. Additionally, polyamine metabolism impacts immunotherapy through its regulation of key enzymes. This review also explores potential therapeutic targets and summarizes the roles of polyamine inhibitors in combination with immunotherapy for cancer treatment, offering a novel perspective on therapeutic strategies.
引用
收藏
页数:15
相关论文
共 106 条
[1]   Loss of Anti-Tumor Efficacy by Polyamine Blocking Therapy in GCN2 Null Mice [J].
Alexander, Eric T. ;
Fahey, Erin ;
Phanstiel, Otto ;
Gilmour, Susan K. .
BIOMEDICINES, 2023, 11 (10)
[2]   Harnessing the polyamine transport system to treat BRAF inhibitor-resistant melanoma [J].
Alexander, Eric T. ;
El Naggar, Olivia ;
Fahey, Erin ;
Mariner, Kelsey ;
Donnelly, Julia ;
Wolfgang, Katelyn ;
Phanstiel, Otto ;
Gilmour, Susan K. .
CANCER BIOLOGY & THERAPY, 2021, 22 (03) :225-237
[3]   Polyamine Blocking Therapy Decreases Survival of Tumor-Infiltrating Immunosuppressive Myeloid Cells and Enhances the Antitumor Efficacy of PD-1 Blockade [J].
Alexander, Eric T. ;
Mariner, Kelsey ;
Donnelly, Julia ;
Phanstiel, Otto ;
Gilmour, Susan K. .
MOLECULAR CANCER THERAPEUTICS, 2020, 19 (10) :2012-2022
[4]  
[Anonymous], European Journal of Immunology, DOI [10.1002/eji.202048784, DOI 10.1002/EJI.202048784]
[5]   Oil for the cancer engine: The cross-talk between oncogenic signaling and polyamine metabolism [J].
Arruabarrena-Aristorena, Amaia ;
Zabala-Letona, Amaia ;
Carracedo, Arkaitz .
SCIENCE ADVANCES, 2018, 4 (01)
[6]   An unexpected pathway to polyamines in pancreatic cancer [J].
Awad, Dominik ;
Lyssiotis, Costas A. .
MOLECULAR CELL, 2023, 83 (11) :1765-1766
[7]   Polyamine synthesis as a target of MYC oncogenes [J].
Bachmann, Andre S. ;
Geerts, Dirk .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (48) :18757-18769
[8]   Glypican-1 is a vehicle for polyamine uptake in mammalian cells -: A pivotal role for nitrosothiol-derived nitric oxide [J].
Belting, M ;
Mani, K ;
Jönsson, M ;
Cheng, F ;
Sandgren, S ;
Jonsson, S ;
Ding, K ;
Delcros, JG ;
Fransson, LÅ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (47) :47181-47189
[9]   Inhibition of the aryl hydrocarbon receptor/polyamine biosynthesis axis suppresses multiple myeloma [J].
Bianchi-Smiraglia, Anna ;
Bagati, Archis ;
Fink, Emily E. ;
Affronti, Hayley C. ;
Lipchick, Brittany C. ;
Moparthy, Sudha ;
Long, Mark D. ;
Rosario, Spencer R. ;
Lightman, Shivana M. ;
Moparthy, Kalyana ;
Wolff, David W. ;
Yun, Dong Hyun ;
Han, Zhannan ;
Polechetti, Anthony ;
Roll, Matthew, V ;
Gitlin, Ilya I. ;
Leonova, Katerina, I ;
Rowsam, Aryn M. ;
Kandel, Eugene S. ;
Gudkov, Andrei, V ;
Bergsagel, P. Leif ;
Lee, Kelvin P. ;
Smiraglia, Dominic J. ;
Nikiforov, Mikhail A. .
JOURNAL OF CLINICAL INVESTIGATION, 2018, 128 (10) :4682-4696
[10]   Lipophilic Lysine-Spermine Conjugates Are Potent Polyamine Transport Inhibitors for Use in Combination with a Polyamine Biosynthesis Inhibitor [J].
Burns, Mark R. ;
Graminski, Gerard F. ;
Weeks, Reitha S. ;
Chen, Yan ;
O'Brien, Thomas G. .
JOURNAL OF MEDICINAL CHEMISTRY, 2009, 52 (07) :1983-1993