Department of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
Cancer Sci. 2014 Jan;105(1):1-8. doi: 10.1111/cas.12314. Epub 2013 Nov 29.
The fact that various immune cells, including macrophages, can be found in tumor tissue has long been known. With the recent introduction of the novel concept of macrophage differentiation into a classically activated phenotype (M1) and an alternatively activated phenotype (M2), the role of tumor-associated macrophages (TAMs) is gradually beginning to be elucidated. Specifically, in human malignant tumors, TAMs that have differentiated into M2 macrophages act as "protumoral macrophages" and contribute to the progression of disease. Based on recent basic and preclinical research, TAMs that have differentiated into protumoral or M2 macrophages are believed to be intimately involved in the angiogenesis, immunosuppression, and activation of tumor cells. In this paper, we specifically discuss both the role of TAMs in human malignant tumors and the cell-cell interactions between TAMs and tumor cells.
长期以来,人们一直知道各种免疫细胞,包括巨噬细胞,可以在肿瘤组织中被发现。随着新型巨噬细胞分化为经典激活表型(M1)和交替激活表型(M2)概念的引入,肿瘤相关巨噬细胞(TAMs)的作用逐渐被阐明。具体来说,在人类恶性肿瘤中,分化为 M2 巨噬细胞的 TAMs 充当“促肿瘤巨噬细胞”,并促进疾病的进展。基于最近的基础和临床前研究,分化为促肿瘤或 M2 巨噬细胞的 TAMs 被认为与血管生成、免疫抑制和肿瘤细胞的激活密切相关。在本文中,我们专门讨论了 TAMs 在人类恶性肿瘤中的作用以及 TAMs 与肿瘤细胞之间的细胞-细胞相互作用。