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M1型和M2型极化巨噬细胞在胶质瘤中的重要性及作为潜在治疗靶点的研究

The Importance of M1-and M2-Polarized Macrophages in Glioma and as Potential Treatment Targets.

作者信息

Ren Jiangbin, Xu Bangjie, Ren Jianghao, Liu Zhichao, Cai Lingyu, Zhang Xiaotian, Wang Weijie, Li Shaoxun, Jin Luhao, Ding Lianshu

机构信息

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.

出版信息

Brain Sci. 2023 Aug 31;13(9):1269. doi: 10.3390/brainsci13091269.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e9c/10526262/523eec0b7b1a/brainsci-13-01269-g001.jpg

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