Macrophages at the interface of the co-evolving cancer ecosystem

被引:149
|
作者
Kloosterman, Daan J. [1 ]
Akkari, Leila [1 ]
机构
[1] Netherlands Canc Inst, Oncode Inst, Div Tumor Biol & Immunol, Plesmanlaan 121, NL-1066CX Amsterdam, Netherlands
关键词
TUMOR-ASSOCIATED MACROPHAGES; TISSUE-RESIDENT MACROPHAGES; TNF-ALPHA; MYELOID CELLS; UP-REGULATION; PROGRESSION; MICROENVIRONMENT; INFLAMMATION; EXPRESSION; EVOLUTION;
D O I
10.1016/j.cell.2023.02.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages are versatile and heterogeneous innate immune cells undertaking central functions in balancing immune responses and tissue repair to maintain homeostasis. This plasticity, once co-opted by malignant outgrowth, orchestrates manifold reciprocal interactions within the tumor microenvironment, fueling the evolution of the cancer ecosystem. Here, we review the multilayered sources of influence that jointly underpin and longitudinally shape tumor-associated macrophage (TAM) phenotypic states in solid neoplasms. We discuss how, in response to these signals, TAMs steer tumor evolution in the context of natural selection, biological dispersion, and treatment resistance. A number of research frontiers to be tackled are laid down in this review to therapeutically exploit the complex roles of TAMs in cancer. Building upon knowledge obtained from currently applied TAM-targeting strategies and using next generation technologies, we propose conceptual advances and novel therapeutic avenues to rewire TAM multifaceted regulation of the co-evolving cancer ecosystem.
引用
收藏
页码:1627 / 1651
页数:25
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