Glioma associated microglia/macrophages, a potential pharmacological target to promote antitumor inflammatory immune response in the treatment of glioblastoma

C. D. Russo, N. Cappoli
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引用次数: 16

Abstract

Glioma associated microglia/macrophages (GAMs) constitute the largest proportion of glioma infiltrating cells, particularly in high grade tumors (i.e., glioblastoma). Once inside the tumors, GAMs usually acquire a specific phenotype of activation that favors tumor growth, angiogenesis and promotes the invasion of normal brain parenchyma. Therefore, treatments that limit or prevent GAMs’ recruitment at the tumor site or modulate their immune activation promoting antitumor activities are expected to exert beneficial effects in glioblastoma. In the present paper, we aim at the revision of pharmacological strategies that interfere with GAMs’ function and are currently proposed as an alternative/additional option to current approved cytotoxic regimens.
胶质瘤相关的小胶质细胞/巨噬细胞,在胶质母细胞瘤治疗中促进抗肿瘤炎症免疫反应的潜在药理学靶点
胶质瘤相关的小胶质细胞/巨噬细胞(GAMs)在胶质瘤浸润细胞中占最大比例,尤其是在高级别肿瘤(即胶质母细胞瘤)中。一旦进入肿瘤,GAM通常会获得一种特定的激活表型,有利于肿瘤生长、血管生成并促进正常脑实质的侵袭。因此,限制或阻止GAM在肿瘤部位募集或调节其免疫激活以促进抗肿瘤活性的治疗有望在胶质母细胞瘤中发挥有益作用。在本文中,我们的目标是修订干扰GAM功能的药理学策略,并目前被提议作为当前批准的细胞毒性方案的替代/额外选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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