Noy Roy, Pollard Jeffrey W
Department of Developmental and Molecular Biology, Center for the Study of Reproductive Biology and Women's Health, Albert Einstein College of Medicine, New York, NY 10461, USA.
Department of Developmental and Molecular Biology, Center for the Study of Reproductive Biology and Women's Health, Albert Einstein College of Medicine, New York, NY 10461, USA; MRC Centre for Reproductive Health, Queen's Medical Research Institute, The University of Edinburgh, Edinburgh EH16 4TJ, UK.
Immunity. 2014 Jul 17;41(1):49-61. doi: 10.1016/j.immuni.2014.06.010.
The tumor microenvironment is a complex ecology of cells that evolves with and provides support to tumor cells during the transition to malignancy. Among the innate and adaptive immune cells recruited to the tumor site, macrophages are particularly abundant and are present at all stages of tumor progression. Clinical studies and experimental mouse models indicate that these macrophages generally play a protumoral role. In the primary tumor, macrophages can stimulate angiogenesis and enhance tumor cell invasion, motility, and intravasation. During monocytes and/or metastasis, macrophages prime the premetastatic site and promote tumor cell extravasation, survival, and persistent growth. Macrophages are also immunosuppressive, preventing tumor cell attack by natural killer and T cells during tumor progression and after recovery from chemo- or immunotherapy. Therapeutic success in targeting these protumoral roles in preclinical models and in early clinical trials suggests that macrophages are attractive targets as part of combination therapy in cancer treatment.
肿瘤微环境是一个复杂的细胞生态系统,在肿瘤细胞向恶性转化过程中不断演变并为其提供支持。在招募到肿瘤部位的先天性和适应性免疫细胞中,巨噬细胞特别丰富,且存在于肿瘤进展的各个阶段。临床研究和实验小鼠模型表明,这些巨噬细胞通常发挥促肿瘤作用。在原发性肿瘤中,巨噬细胞可刺激血管生成,并增强肿瘤细胞的侵袭、迁移和血管内渗。在单核细胞和/或转移过程中,巨噬细胞使前转移部位致敏,并促进肿瘤细胞外渗、存活和持续生长。巨噬细胞还具有免疫抑制作用,在肿瘤进展期间以及化疗或免疫治疗恢复后,可阻止自然杀伤细胞和T细胞对肿瘤细胞的攻击。在临床前模型和早期临床试验中,针对这些促肿瘤作用的治疗成功表明,巨噬细胞作为癌症联合治疗的一部分是有吸引力的靶点。