ICI-based therapies: A new strategy for oral potentially malignant disorders

被引:7
|
作者
Wang, Tianqing [1 ]
Sun, Silu [1 ]
Zeng, Xin [1 ,2 ]
Li, Jing [1 ,3 ]
机构
[1] Sichuan Univ, West China Hosp Stomatol, Chinese Acad Med Sci, Natl Clin Res Ctr Oral Dis,State Key Lab Oral Dis,, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp Stomatol, Natl Clin Res Ctr Oral Dis, Dept Oral Med,State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, Natl Clin Res Ctr Oral Dis, State Key Lab Oral Dis, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
OPMDs; ICIs; Immunosuppressive microenvironment; PD-1; cGAS-STING; SQUAMOUS-CELL CARCINOMA; PROMOTES TUMOR PROGRESSION; EXPRESSION; HEAD; ANTITUMOR; MICROENVIRONMENT; NIVOLUMAB; VISTA; MOLECULES; PREDICT;
D O I
10.1016/j.oraloncology.2023.106388
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oral potentially malignant disorders (OPMDs) are linked with an escalated risk of developing cancers, particularly oral squamous cell carcinoma (OSCC). Since prevailing therapies cannot effectively forestall the exacerbation and recurrence of OPMDs, halting their malignant progression is paramount. The immune checkpoint serves as a cardinal regulator of the immune response and the primary cause of adaptive immunological resistance. Although the exact mechanism remains elusive, elevated expression of multiple immune checkpoints in OPMDs and OSCC relative to healthy oral mucosa has been ascertained. This review delves into the immunosuppressive microenvironment of OPMDs, the expression of diverse immune checkpoints such as programmed death receptor-1 (PD-1) and programmed death receptor-1 ligand (PD-L1) in OPMDs, and the potential application of corresponding inhibitors. In addition, synergistic strategies incorporating combined immune checkpoint inhibitors, such as cGAS-STING, costimulatory molecules, cancer vaccines, and hydrogels, are discussed to gain a more comprehensive understanding of the role and application of immune checkpoint inhibitors (ICIs) in oral carcinogenesis.
引用
收藏
页数:10
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