School of Life and Environmental Sciences, Shaoxing University, Shaoxing, 312000, Zhejiang, China.
Department of Fundamental Oncology, Faculty of Biology and Medicine, University of Lausanne, Lausanne, Switzerland.
J Exp Clin Cancer Res. 2023 Sep 23;42(1):245. doi: 10.1186/s13046-023-02832-9.
Macrophages are highly plastic in different tissues and can differentiate into functional subpopulations under different stimuli. Tumor-associated macrophages (TAMs) are one of the most important innate immune cells implicated in the establishment of an immunosuppressive tumor microenvironment (TME). Recent evidence pinpoints the critical role of metabolic reprogramming in dictating pro-tumorigenic functions of TAMs. Both tumor cells and macrophages undergo metabolic reprogramming to meet energy demands in the TME. Understanding the metabolic rewiring in TAMs can shed light on immune escape mechanisms and provide insights into repolarizing TAMs towards anti-tumorigenic function. Here, we discuss how metabolism impinges on the functional divergence of macrophages and its relevance to macrophage polarization in the TME.
巨噬细胞在不同组织中具有高度的可塑性,并能在不同刺激下分化为具有功能的亚群。肿瘤相关巨噬细胞(TAMs)是参与建立免疫抑制性肿瘤微环境(TME)的最重要的固有免疫细胞之一。最近的证据指出,代谢重编程在决定 TAMs 的促肿瘤功能方面起着关键作用。肿瘤细胞和巨噬细胞都经历代谢重编程以满足 TME 中的能量需求。了解 TAMs 中的代谢重排可以揭示免疫逃逸机制,并深入了解将 TAMs 重新极化为抗肿瘤功能。在这里,我们讨论代谢如何影响巨噬细胞的功能分化及其与 TME 中巨噬细胞极化的相关性。