Role of tumor microenvironment in cancer progression and therapeutic strategy

被引:70
|
作者
Wang, Qingjing [1 ]
Shao, Xueting [2 ,3 ]
Zhang, Yuxuan [1 ]
Zhu, Miaojin [4 ]
Wang, Frederick X. C. [5 ]
Mu, Jianjian [1 ]
Li, Jiaxuan [1 ]
Yao, Hangping [4 ]
Chen, Keda [1 ]
机构
[1] Zhejiang Shuren Univ, Shulan Int Med Coll, Hangzhou, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Inst Pharmaceut Biotechnol, Sch Med, Hangzhou, Peoples R China
[3] Zhejiang Univ, Affiliated Hosp 1, Res Ctr Clin Pharm, Sch Med, Hangzhou, Peoples R China
[4] Zhejiang Univ, Affiliated Hosp 1, Natl Clin Res Ctr Infect Dis, Sch Med, Hangzhou, Peoples R China
[5] Texas A&M Univ, EnMed Program Houston Methodist Hosp, Coll Engn, Coll Med, Houston, TX USA
来源
CANCER MEDICINE | 2023年 / 12卷 / 10期
基金
中国国家自然科学基金;
关键词
cancer immunotherapy; cancer progression; PD-1; PD-L1; tumor microenvironment; T-CELL THERAPY; METABOLIC INTERACTIONS; OVERCOMES RESISTANCE; ANTI-PD-1; THERAPY; SOLID TUMORS; IMMUNOTHERAPY; PD-L1; MICROBIOME; EXPRESSION; BLOCKADE;
D O I
10.1002/cam4.5698
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer is now considered a tumor microenvironment (TME) disease, although it was originally thought to be a cell and gene expression disorder. Over the past 20 years, significant advances have been made in understanding the complexity of the TME and its impact on responses to various anticancer therapies, including immunotherapies. Cancer immunotherapy can recognize and kill cancer cells by regulating the body's immune system. It has achieved good therapeutic effects in various solid tumors and hematological malignancies. Recently, blocking of programmed death-1 (PD-1), programmed death-1 ligand-1 (PD-L1), and programmed death Ligand-2 (PD-L2), the construction of antigen chimeric T cells (CAR-T) and tumor vaccines have become popular immunotherapies Tumorigenesis, progression, and metastasis are closely related to TME. Therefore, we review the characteristics of various cells and molecules in the TME, the interaction between PD-1 and TME, and promising cancer immunotherapy therapeutics.
引用
收藏
页码:11149 / 11165
页数:17
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