The roles of glioma-associated macrophages/microglia and potential targets for anti-glioma therapy

被引:0
|
作者
Matsuzaki, Hiroaki [1 ,2 ]
Pan, Cheng [1 ]
Komohara, Yoshihiro [1 ]
Yamada, Rin [1 ,3 ]
Yano, Hiromu [1 ]
Fujiwara, Yukio [1 ]
Kai, Keitaro [2 ]
Mukasa, Akitake [2 ]
机构
[1] Kumamoto Univ, Grad Sch Med Sci, Dept Cell Pathol, 1-1-1 Honjo Chuo Ku, Kumamoto 8608556, Japan
[2] Kumamoto Univ, Grad Sch Med Sci, Dept Neurosurg, Kumamoto, Japan
[3] Kumamoto Univ, Grad Sch Med Sci, Dept Diagnost Pathol, Kumamoto, Japan
关键词
Tumor-associated macrophage (TAM); microglia; brain tumor; glioblastoma; MONOCYTE CHEMOATTRACTANT PROTEIN-1; COLONY-STIMULATING FACTOR; MACROPHAGE INFILTRATION; EXPRESSION; MICROGLIA; BEVACIZUMAB; BIOLOGY; GROWTH;
D O I
10.1080/25785826.2024.2411035
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Glioblastoma (GBM) is the central nervous system tumor with the most aggressive behavior, and no definitive therapy has yet been found. The tumor microenvironment of GBM is immunosuppressive and is considered a 'cold tumor' with low lymphocytic infiltration, but is characterized by a high proportion of glioma-associated macrophages/microglia (GAMs). GAMs promote tumor growth and also affect treatment resistance in GBM. In this review, we describe the origin and classification of GAMs in humans and describe the mechanisms of their activation and the cell-cell interactions between tumor cells and GAMs. We also describe the history of GAM detection methods, especially immunohistochemistry, and discusses the merits and limitations of these techniques. In addition, we summarized chemotactic factors for GAMs and the therapies targeting these factors. Recent single-cell RNA analysis and spatial analysis add new insights to our previous knowledge of GAMs. Based on these studies, GBM therapies targeting GAMs are expected to be further developed.
引用
收藏
页码:24 / 32
页数:9
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