Tumor microenvironment and immune-related therapies of head and neck squamous cell carcinoma

被引:56
作者
Qin, Yixiao [1 ,2 ]
Zheng, Xiwang [1 ,3 ]
Gao, Wei [1 ,2 ,3 ,4 ,5 ]
Wang, Binquan [1 ,2 ,3 ]
Wu, Yongyan [1 ,2 ,3 ,4 ,6 ]
机构
[1] Shanxi Med Univ, Hosp 1, Shanxi Key Lab Otorhinolaryngol Head & Neck Canc, Taiyuan 030001, Shanxi, Peoples R China
[2] Shanxi Med Univ, Hosp 1, Dept Otolaryngol Head & Neck Surg, Taiyuan 030001, Shanxi, Peoples R China
[3] Shanxi Med Univ, Hosp 1, Shanxi Prov Clin Med Res Ctr Precis Med Head & Ne, Taiyuan 030001, Shanxi, Peoples R China
[4] Shanxi Med Univ, Key Lab Cellular Physiol, Minist Educ, Taiyuan 030001, Shanxi, Peoples R China
[5] Shanxi Med Univ, Basic Med Sch, Dept Cell Biol & Genet, Taiyuan 030001, Shanxi, Peoples R China
[6] Shanxi Med Univ, Dept Biochem & Mol Biol, Taiyuan 030001, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
CANCER-ASSOCIATED FIBROBLASTS; REGULATORY T-CELLS; NATURAL-KILLER-CELLS; SUPPRESSOR-CELLS; MACROPHAGE PLASTICITY; DENDRITIC CELLS; POOR-PROGNOSIS; OPEN-LABEL; IMMUNOTHERAPY; EXPRESSION;
D O I
10.1016/j.omto.2021.01.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Head and neck squamous cell carcinomas (HNSCCs) are a type of common malignant tumor, mainlymanifesting as oropharyngeal, oral cavity, laryngopharyngeal, hypopharyngeal, and laryngeal cancers. These highly aggressive malignant tumors reportedly affect more than 830,000 patients worldwide every year. Currently, the main treatments for HNSCC include surgery, radiotherapy, chemotherapy, and immunotherapy, as well as combination therapy. However, the overall 5-year survival rate of HNSCC has remained 50%, and it has not significantly improved in the past 10 years. Previous studies have shown that the tumor microenvironment (TME) plays a crucial role in the recurrence, metastasis, and drug resistance of patients with HNSCC. In this review, we summarize the role of anti-tumor and pro-tumor immune cells, as well as extracellular components in the TME of HNSCC. We also discuss classical HNSCC immunotherapy and highlight examples of clinical trials using CTLA-4 inhibitors and programmed cell death 1 (PD1)/programmed cell death ligand 1 (PD-L1)-related combination therapies. We also outline somemolecules in the TME known to regulate immunosuppressive cells. Furthermore, the role and underlying mechanism of radiation therapy on the TME, immune cells, and immune response are discussed.
引用
收藏
页码:342 / 351
页数:10
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