Ren Jiangbin, Xu Bangjie, Ren Jianghao, Liu Zhichao, Cai Lingyu, Zhang Xiaotian, Wang Weijie, Li Shaoxun, Jin Luhao, Ding Lianshu
Department of neurosurgery, The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Nanjing Medical University, Huai'an 223000, China.
Department of Thoracic Surgery, Shanghai Chest Hospital, Shanghai Jiaotong University, Shanghai 200030, China.
Brain Sci. 2023 Aug 31;13(9):1269. doi: 10.3390/brainsci13091269.
Glioma is the most common and malignant tumor of the central nervous system. Glioblastoma (GBM) is the most aggressive glioma, with a poor prognosis and no effective treatment because of its high invasiveness, metabolic rate, and heterogeneity. The tumor microenvironment (TME) contains many tumor-associated macrophages (TAMs), which play a critical role in tumor proliferation, invasion, metastasis, and angiogenesis and indirectly promote an immunosuppressive microenvironment. TAM is divided into tumor-suppressive M1-like (classic activation of macrophages) and tumor-supportive M2-like (alternatively activated macrophages) polarized cells. TAMs exhibit an M1-like phenotype in the initial stages of tumor progression, and along with the promotion of lysing tumors and the functions of T cells and NK cells, tumor growth is suppressed, and they rapidly transform into M2-like polarized macrophages, which promote tumor progression. In this review, we discuss the mechanism by which M1- and M2-polarized macrophages promote or inhibit the growth of glioblastoma and indicate the future directions for treatment.
胶质瘤是中枢神经系统最常见的恶性肿瘤。胶质母细胞瘤(GBM)是最具侵袭性的胶质瘤,由于其高侵袭性、代谢率和异质性,预后较差且没有有效的治疗方法。肿瘤微环境(TME)包含许多肿瘤相关巨噬细胞(TAM),它们在肿瘤增殖、侵袭、转移和血管生成中起关键作用,并间接促进免疫抑制微环境。TAM分为具有肿瘤抑制作用的M1样(巨噬细胞的经典激活)和具有肿瘤支持作用的M2样(替代性激活的巨噬细胞)极化细胞。TAM在肿瘤进展的初始阶段表现出M1样表型,随着肿瘤溶解以及T细胞和NK细胞功能的促进,肿瘤生长受到抑制,它们迅速转变为促进肿瘤进展的M2样极化巨噬细胞。在本综述中,我们讨论了M1和M2极化巨噬细胞促进或抑制胶质母细胞瘤生长的机制,并指出了未来的治疗方向。