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肿瘤免疫治疗中CD73抑制剂的研发以及成像与联合治疗的机遇

Development of CD73 Inhibitors in Tumor Immunotherapy and Opportunities in Imaging and Combination Therapy.

作者信息

Bi Chunyang, Patel Jimmy S, Liang Steven H

机构信息

Department of Radiology and Imaging Sciences, Emory University, Atlanta, Georgia 30322, United States.

PharmaCenter Bonn, Pharmaceutical Institute, Pharmaceutical & Medicinal Chemistry, University of Bonn, An der Immenburg 4, D-53121 Bonn, Germany.

出版信息

J Med Chem. 2025 Apr 10;68(7):6860-6869. doi: 10.1021/acs.jmedchem.4c02151. Epub 2025 Mar 19.


DOI:10.1021/acs.jmedchem.4c02151
PMID:40106690
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11998006/
Abstract

CD73 is a member of the membrane-bound enucleotidase family, which catalyzes the extracellular hydrolysis of adenosine monophosphate (AMP) to produce anti-inflammatory and immunosuppressive adenosine. As a novel checkpoint protein, CD73 is overexpressed in the immune system of various tumors, where adenosine is abundantly enriched. A large number of monoclonal antibodies (mAbs), nucleotides, and non-nucleotides as potent CD73 inhibitors are being discovered, providing opportunities for novel tumor immunotherapy. Currently, 18 CD73 inhibitors are in clinical trials, showing promising results in combination therapy for various solid tumors. The development of CD73-specific companion positron emission tomography imaging ligands holds potential for facilitating diagnosis, patient selection, and treatment efficacy evaluation throughout the entire process of CD73-targeted therapeutic development.

摘要

CD73是膜结合核苷磷酸酶家族的一员,它催化细胞外单磷酸腺苷(AMP)水解,产生抗炎和免疫抑制性腺苷。作为一种新型的检查点蛋白,CD73在多种肿瘤的免疫系统中过度表达,腺苷在这些肿瘤中大量富集。大量作为强效CD73抑制剂的单克隆抗体(mAb)、核苷酸和非核苷酸正在被发现,这为新型肿瘤免疫治疗提供了机会。目前,有18种CD73抑制剂正在进行临床试验,在各种实体瘤的联合治疗中显示出有前景的结果。开发CD73特异性的伴随正电子发射断层扫描成像配体,在CD73靶向治疗开发的整个过程中,对于促进诊断、患者选择和治疗疗效评估具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/596b4fbc2b91/jm4c02151_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/610b3c9f04ea/jm4c02151_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/cf90f99c9447/jm4c02151_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/a3f43769ad83/jm4c02151_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/596b4fbc2b91/jm4c02151_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/610b3c9f04ea/jm4c02151_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/cf90f99c9447/jm4c02151_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/a3f43769ad83/jm4c02151_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f71c/11998006/596b4fbc2b91/jm4c02151_0004.jpg

相似文献

[1]
Development of CD73 Inhibitors in Tumor Immunotherapy and Opportunities in Imaging and Combination Therapy.

J Med Chem. 2025-4-10

[2]
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Bioorg Med Chem Lett. 2024-11-1

[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Non-Canonical Functions of Adenosine Receptors: Emerging Roles in Metabolism, Immunometabolism, and Epigenetic Regulation.

Int J Mol Sci. 2025-7-26

本文引用的文献

[1]
Discovery of Novel 5-(Pyridazin-3-yl)pyrimidine-2,4(1,3)-dione Derivatives as Potent and Orally Bioavailable Inhibitors Targeting Ecto-5'-nucleotidase.

J Med Chem. 2024-10-24

[2]
Discovery of Novel Non-Nucleoside Inhibitors Interacting with Dizinc Ions of CD73.

J Med Chem. 2024-6-13

[3]
MDSCs in bone metastasis: Mechanisms and therapeutic potential.

Cancer Lett. 2024-6-28

[4]
A novel small molecule inhibitor of CD73 triggers immune-mediated multiple myeloma cell death.

Blood Cancer J. 2024-4-9

[5]
Small molecular CD73 inhibitors: Recent progress and future perspectives.

Eur J Med Chem. 2024-1-15

[6]
The Clinical Significance of CD73 in Cancer.

Int J Mol Sci. 2023-7-21

[7]
Overexpression of CD73 is associated with recurrence and poor prognosis of gingivobuccal oral cancer as revealed by transcriptome and deep immune profiling of paired tumor and margin tissues.

Cancer Med. 2023-8

[8]
Advances in CD73 inhibitors for immunotherapy: Antibodies, synthetic small molecule compounds, and natural compounds.

Eur J Med Chem. 2023-10-5

[9]
Radiochemistry for positron emission tomography.

Nat Commun. 2023-6-5

[10]
The CD73 immune checkpoint promotes tumor cell metabolic fitness.

Elife. 2023-6-1

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