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The Fate of the Tumor in the Hands of Microenvironment: Role of TAMs and mTOR Pathway

机译:微环境手中的肿瘤命运:TAM和mTOR通路的作用

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摘要

Since 2000, written with elegance and accuracy, Hanahan and Weinberg have proposed six major hallmarks of cancer and, together, they provide great advances to the understanding of tumoral biology. Our knowledge about tumor behavior has improved and the investigators have now recognized that inflammatory microenvironment may be a new feature for the tumor entities. Macrophages are considered as an important component of tumoral microenvironment. Biologically, two forms of activated macrophages can be observed: classically activated macrophages (M1) and alternative activated macrophages (M2). Despite the canonical pathways that control this puzzle of macrophages polarization, recently, mTOR signaling pathway has been implicated as an important piece in determining the metabolic and functional differentiation of M1 and M2 profiles. Currently, it is believed that macrophages related to tumoral microenvironment present an “M2-like” feature promoting an immunosuppressive microenvironment enhancing tumoral angiogenesis, growth, and metastasis. In the present review we discuss the role of macrophages in the tumor microenvironment and the role of mTOR pathway in M1 and M2 differentiation. We also discuss the recent findings in M1 and M2 polarization as a possible target in the cancer therapy.
机译:自2000年以来,Hanahan和Weinberg用优雅而准确的文字提出了六种癌症的主要标志,它们一起为理解肿瘤生物学提供了巨大的进步。我们对肿瘤行为的了解有所提高,研究人员现已认识到,炎症微环境可能是肿瘤实体的新特征。巨噬细胞被认为是肿瘤微环境的重要组成部分。从生物学上讲,可以观察到两种形式的活化巨噬细胞:经典活化巨噬细胞(M1)和替代活化巨噬细胞(M2)。尽管控制巨噬细胞极化这个难题的规范途径,最近,mTOR信号传导途径已被认为是确定M1和M2谱的代谢和功能分化的重要部分。当前,据信与肿瘤微环境有关的巨噬细胞呈现出“ M2样”特征,其促进免疫抑制性微环境增强了肿瘤血管生成,生长和转移。在本综述中,我们讨论了巨噬细胞在肿瘤微环境中的作用以及mTOR通路在M1和M2分化中的作用。我们还将讨论M1和M2极化的最新发现,将其作为癌症治疗中的可能靶标。

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