Targeting Endocytosis and Cell Communications in the Tumor Immune Microenvironment

被引:10
作者
Wu, Bo [1 ]
Wang, Qian [2 ]
Shi, Xiang [3 ]
Jiang, Meixi [4 ]
机构
[1] China Med Univ, Affiliated Hosp 4, Dept Gen Surg, Shenyang 110032, Peoples R China
[2] Fifth Hosp Xiamen, Dept Radiol, Xiamen 361101, Peoples R China
[3] China Med Univ, Canc Hosp Liaoning Prov, Dept Thorac Surg, Shenyang 110032, Peoples R China
[4] China Med Univ, Affiliated Hosp 4, Dept Neurol, Shenyang 110032, Peoples R China
基金
中国国家自然科学基金;
关键词
Endocytosis; Tumor immune microenvironment; Adhesion molecules; Exosome; HEPATOCELLULAR-CARCINOMA; EXTRACELLULAR VESICLES; CANCER PROGRESSION; B-CELLS; EXOSOMES; SECRETION; SYNAPSE; PROTEINS; MACROPINOCYTOSIS; MICROVESICLES;
D O I
10.1186/s12964-022-00968-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The existence of multiple endocytic pathways is well known, and their exact biological effects in tumors have been intensively investigated. Endocytosis can affect the connection between tumor cells and determine the fate of tumor cells. Many relationships between endocytosis and tumor cells have been elucidated, but the mechanism of endocytosis between different types of cells in tumors needs to be explored in greater depth. Endocytic receptors sense the environment and are induced by specific ligands to trigger communication between tumor and immune cells. Crosstalk in the tumor microenvironment can occur through direct contact between cell adhesion molecules or indirectly through exosomes. So a better understanding of the endocytic pathways that control cell adhesion molecules and function is expected to lead to new candidates for cancer treatment. In additional, tumor-derived exosomes may changes immune cell function, which may be a key role for tumors to evade immune detection and response. The overall understanding of exosomes through endocytosis is also expected to bring new candidates for therapeutic regulation of tumor immune microenvironment. In this case, endocytic pathways coordinate cell adhesion molecules and exosomes and can be used as targets in the tumor immune microenvironment for cancer treatment.
引用
收藏
页数:10
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