Targeting Tumor Microenvironment by Small-Molecule Inhibitors

被引:78
|
作者
Zhong, Shangwei [1 ,2 ]
Jeong, Ji-Hak [2 ]
Chen, Zhikang [1 ]
Chen, Zihua [1 ]
Luo, Jun-Li [2 ]
机构
[1] Cent South Univ, Xiangya Hosp, Hunan Prov Key Lab Precis Diag & Treatment Gastro, Changsha 410008, Hunan, Peoples R China
[2] Scripps Res Inst, Dept Mol Med, Jupiter, FL 33458 USA
来源
TRANSLATIONAL ONCOLOGY | 2020年 / 13卷 / 01期
关键词
CANCER-ASSOCIATED FIBROBLASTS; CARBONIC-ANHYDRASE IX; REGULATORY T-CELLS; CARCINOMA-ASSOCIATED FIBROBLASTS; HYPOXIA-ACTIVATED PRODRUG; TYROSINE KINASE INHIBITOR; ENDOTHELIAL GROWTH-FACTOR; PROTON PUMP INHIBITORS; ANTITUMOR-ACTIVITY; SUPPRESSOR-CELL;
D O I
10.1016/j.tranon.2019.10.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The tumor microenvironment (TME) is a hypoxic, acidic, and immune/inflammatory cell-enriched milieu that plays crucial roles in tumor development, growth, progression, and therapy resistance. Targeting TME is an attractive strategy for the treatment of solid tumors. Conventional cancer chemotherapies are mostly designed to directly kill cancer cells, and the effectiveness is always compromised by their penetration and accessibility to cancer cells. Small-molecule inhibitors, which exhibit good penetration and accessibility, are widely studied, and many of them have been successfully applied in clinics for cancer treatment. As TME is more penetrable and accessible than tumor cells, a lot of efforts have recently been made to generate small-molecule inhibitors that specifically target TME or the components of TME or develop special drug-delivery systems that release the cytotoxic drugs specifically in TME. In this review, we briefly summarize the recent advances of small-molecule inhibitors that target TME for the tumor treatment.
引用
收藏
页码:57 / 69
页数:13
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