Department of Molecular, Cellular and Biomedical Sciences, University of New Hampshire, Durham, NH 03824, USA.
Int J Mol Sci. 2021 Jun 29;22(13):6995. doi: 10.3390/ijms22136995.
The M1/M2 macrophage paradigm plays a key role in tumor progression. M1 macrophages are historically regarded as anti-tumor, while M2-polarized macrophages, commonly deemed tumor-associated macrophages (TAMs), are contributors to many pro-tumorigenic outcomes in cancer through angiogenic and lymphangiogenic regulation, immune suppression, hypoxia induction, tumor cell proliferation, and metastasis. The tumor microenvironment (TME) can influence macrophage recruitment and polarization, giving way to these pro-tumorigenic outcomes. Investigating TME-induced macrophage polarization is critical for further understanding of TAM-related pro-tumor outcomes and potential development of new therapeutic approaches. This review explores the current understanding of TME-induced macrophage polarization and the role of M2-polarized macrophages in promoting tumor progression.
M1/M2 巨噬细胞范式在肿瘤进展中起着关键作用。M1 巨噬细胞在历史上被认为是抗肿瘤的,而 M2 极化的巨噬细胞,通常被认为是肿瘤相关巨噬细胞 (TAMs),通过血管生成和淋巴管生成调节、免疫抑制、缺氧诱导、肿瘤细胞增殖和转移,促进了许多促肿瘤发生的结果。肿瘤微环境 (TME) 可以影响巨噬细胞的募集和极化,从而导致这些促肿瘤发生的结果。研究 TME 诱导的巨噬细胞极化对于进一步了解 TAM 相关促肿瘤发生的结果和潜在的新治疗方法的发展至关重要。这篇综述探讨了 TME 诱导的巨噬细胞极化的现有理解,以及 M2 极化的巨噬细胞在促进肿瘤进展中的作用。