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Microglia and macrophage metabolism: a regulator of cerebral gliomas.
Deng, Yue; Chen, Qinyan; Wan, Chao; Sun, Yajie; Huang, Fang; Hu, Yan; Yang, Kunyu.
Afiliación
  • Deng Y; Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
  • Chen Q; Hubei Key Laboratory of Precision Radiation Oncology, Wuhan, 430022, China.
  • Wan C; Institute of Radiation Oncology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
  • Sun Y; Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
  • Huang F; Hubei Key Laboratory of Precision Radiation Oncology, Wuhan, 430022, China.
  • Hu Y; Institute of Radiation Oncology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
  • Yang K; Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Cell Biosci ; 14(1): 49, 2024 Apr 17.
Article en En | MEDLINE | ID: mdl-38632627
ABSTRACT
Reciprocal interactions between the tumor microenvironment (TME) and cancer cells play important roles in tumorigenesis and progression of glioma. Glioma-associated macrophages (GAMs), either of peripheral origin or representing brain-intrinsic microglia, are the majority population of infiltrating immune cells in glioma. GAMs, usually classified into M1 and M2 phenotypes, have remarkable plasticity and regulate tumor progression through different metabolic pathways. Recently, research efforts have increasingly focused on GAMs metabolism as potential targets for glioma therapy. This review aims to delineate the metabolic characteristics of GAMs within the TME and provide a summary of current therapeutic strategies targeting GAMs metabolism in glioma. The goal is to provide novel insights and therapeutic pathways for glioma by highlighting the significance of GAMs metabolism.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Cell Biosci Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Cell Biosci Año: 2024 Tipo del documento: Article País de afiliación: China