دورية أكاديمية

Development of small molecule drugs targeting immune checkpoints.

التفاصيل البيبلوغرافية
العنوان: Development of small molecule drugs targeting immune checkpoints.
المؤلفون: Chen L; Department of Oncology, Sichuan Academy of Medical Sciences, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610054, China., Zhao X; Department of Oncology, Sichuan Academy of Medical Sciences, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610054, China., Liu X; Institute for Breast Health Medicine, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China., Ouyang Y; Acupuncture and Massage College, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China., Xu C; Department of Oncology, Sichuan Academy of Medical Sciences, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610054, China., Shi Y; Department of Oncology, Sichuan Academy of Medical Sciences, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610054, China.
المصدر: Cancer biology & medicine [Cancer Biol Med] 2024 May 09; Vol. 21 (5).
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Chinese Anti-Cancer Association Country of Publication: China NLM ID: 101588850 Publication Model: Print Cited Medium: Internet ISSN: 2095-3941 (Print) Linking ISSN: 20953941 NLM ISO Abbreviation: Cancer Biol Med Subsets: MEDLINE
أسماء مطبوعة: Original Publication: [Tianjin] : Chinese Anti-Cancer Association
مواضيع طبية MeSH: Immune Checkpoint Inhibitors*/therapeutic use , Neoplasms*/drug therapy , Neoplasms*/immunology, Humans ; Drug Development ; Immune Checkpoint Proteins/metabolism ; Small Molecule Libraries/pharmacology ; Animals ; Immunotherapy/methods
مستخلص: Immune checkpoint inhibitors (ICIs) are used to relieve and refuel anti-tumor immunity by blocking the interaction, transcription, and translation of co-inhibitory immune checkpoints or degrading co-inhibitory immune checkpoints. Thousands of small molecule drugs or biological materials, especially antibody-based ICIs, are actively being studied and antibodies are currently widely used. Limitations, such as anti-tumor efficacy, poor membrane permeability, and unneglected tolerance issues of antibody-based ICIs, remain evident but are thought to be overcome by small molecule drugs. Recent structural studies have broadened the scope of candidate immune checkpoint molecules, as well as innovative chemical inhibitors. By way of comparison, small molecule drug-based ICIs represent superior oral bioavailability and favorable pharmacokinetic features. Several ongoing clinical trials are exploring the synergetic effect of ICIs and other therapeutic strategies based on multiple ICI functions, including immune regulation, anti-angiogenesis, and cell cycle regulation. In this review we summarized the current progression of small molecule ICIs and the mechanism underlying immune checkpoint proteins, which will lay the foundation for further exploration.
Competing Interests: No potential conflicts of interest are disclosed.
(Copyright: © 2024, The Authors.)
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معلومات مُعتمدة: 82203539 National Natural Science Foundation of China; 92259102 National Natural Science Foundation of China; 2023YFSY0043 Provincial Cooperation Project of Science and Technology Department of Sichuan Province; 2023YFC3402100 National Key Research and Development Program of China
فهرسة مساهمة: Keywords: CD47; Immune checkpoints; programmed death protein 1; signal-regulatory protein α; small molecule drugs
المشرفين على المادة: 0 (Immune Checkpoint Inhibitors)
0 (Immune Checkpoint Proteins)
0 (Small Molecule Libraries)
تواريخ الأحداث: Date Created: 20240510 Date Completed: 20240528 Latest Revision: 20240530
رمز التحديث: 20240530
مُعرف محوري في PubMed: PMC11131045
DOI: 10.20892/j.issn.2095-3941.2024.0034
PMID: 38727005
قاعدة البيانات: MEDLINE
الوصف
تدمد:2095-3941
DOI:10.20892/j.issn.2095-3941.2024.0034