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The contribution of tumor-associated macrophages in glioma neo-angiogenesis and implications for anti-angiogenic strategies

机译:肿瘤相关巨噬细胞在神经胶质瘤新血管生成中的作用及其对抗血管生成策略的影响

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摘要

“Tumor-associated macrophages” (TAMs) form a significant cell population in malignant tumors and contribute to tumor growth, metastasis, and neovascularization. Gliomas are characterized by extensive neo-angiogenesis, and knowledge of the role of TAMs in neovascularization is important for future anti-angiogenic therapies. The phenotypes and functions of TAMs are heterogeneous and more complex than a classification into M1 and M2 inflammation response types would suggest. In this review, we provide an update on the current knowledge of the ontogeny of TAMs, focusing on diffuse gliomas. The role of TAMs in the regulation of the different processes in tumor angiogenesis is highlighted and the most recently discovered mechanisms by which TAMs mediate resistance against current antivascular therapies are mentioned. Novel compounds tested in clinical trials are discussed and brought in relation to different TAM-related angiogenesis pathways. In addition, potential therapeutic targets used to intervene in TAM-regulated tumor angiogenesis are summarized.
机译:“肿瘤相关巨噬细胞”(TAM)在恶性肿瘤中形成大量细胞,并有助于肿瘤生长,转移和新血管形成。神经胶质瘤的特征在于广泛的新血管生成,并且TAM在新血管形成中的作用的知识对于未来的抗血管生成疗法很重要。 TAM的表型和功能是异质的,并且比分类为M1和M2炎症反应类型所提示的更为复杂。在这篇综述中,我们提供了有关TAM的个体发育的最新知识,重点是弥漫性神经胶质瘤。强调了TAM在调节肿瘤血管生成中不同过程中的作用,并提及了最近发现的TAM介导对当前抗血管疗法的抗性的机制。讨论了在临床试验中测试的新型化合物,并将其与不同的TAM相关的血管生成途径相关。此外,总结了用于干预TAM调节的肿瘤血管生成的潜在治疗靶标。

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