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CD155 as an emerging target in tumor immunotherapy
Jiang-Wan Wu1, Ying Liu2, Xing-Jie Dai1
1State Key Laboratory of Esophageal Cancer Prevention & Treatment, Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education of China, Key Laboratory of Henan Province for Drug Quality and Evaluation, XNA Platform, School of Pharmaceutical Sciences, Zhengzhou University, 100 Kexue Avenue, Zhengzhou, Henan 450001, China.
CD155, a protein on tumor cells, drives cancer growth and immune evasion. Inhibiting CD155/TIGIT shows promise for treating advanced solid tumors, paving the way for new immunotherapies.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- CD155 (also known as PVR) is an immunoglobulin-like protein frequently overexpressed on tumor cells.
- It promotes tumor cell proliferation, adhesion, invasion, and migration.
- CD155 interacts with immune receptors TIGIT, CD226, and CD96, modulating immune cell function and contributing to tumor immune escape.
Purpose of the Study:
- To review the relationship between tumor surface CD155 and its receptors.
- To discuss how these interactions regulate tumor immune escape.
- To summarize novel therapeutic strategies and clinical trials targeting CD155 and its receptors for cancer immunotherapy.
Main Methods:
- Literature review of studies on CD155 function in cancer.
- Analysis of the molecular interactions between CD155 and immune receptors (TIGIT, CD226, CD96).
- Summary of preclinical and clinical data for CD155-targeted therapies.
Main Results:
- CD155 plays a critical role in promoting tumor progression and immune evasion.
- Inhibition of the CD155/TIGIT pathway demonstrates efficacy in advanced solid malignancies.
- Combination therapies involving CD155/TIGIT inhibition show potential.
Conclusions:
- CD155 is a key target for overcoming tumor immune escape.
- Targeting CD155 and its receptors offers a promising strategy for next-generation cancer immunotherapies.
- Further clinical investigation of CD155-targeted therapies is warranted.
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