Coffelt Seth B, Hughes Russell, Lewis Claire E
Academic Unit of Pathology, Medical School, University of Sheffield, Sheffield, UK.
Biochim Biophys Acta. 2009 Aug;1796(1):11-8. doi: 10.1016/j.bbcan.2009.02.004. Epub 2009 Mar 6.
Tumor-associated macrophages (TAMs) are a prominent inflammatory cell population in many tumor types residing in both perivascular and avascular, hypoxic regions of these tissues. Analysis of TAMs in human tumor biopsies has shown that they express a variety of tumor-promoting factors and evidence from transgenic murine tumor models has provided unequivocal evidence for the importance of these cells in driving angiogenesis, lymphangiogenesis, immunosuppression, and metastasis. This review will summarize the mechanisms by which monocytes are recruited into tumors, their myriad, tumor-promoting functions within tumors, and the influence of the tumor microenvironment in driving these activities. We also discuss recent attempts to both target/destroy TAMs and exploit them as delivery vehicles for anti-cancer gene therapy.
肿瘤相关巨噬细胞(TAM)是许多肿瘤类型中突出的炎症细胞群体,存在于这些组织的血管周围和无血管的缺氧区域。对人类肿瘤活检组织中TAM的分析表明,它们表达多种肿瘤促进因子,转基因小鼠肿瘤模型的证据明确证实了这些细胞在驱动血管生成、淋巴管生成、免疫抑制和转移中的重要性。本综述将总结单核细胞被募集到肿瘤中的机制、它们在肿瘤内众多的促肿瘤功能,以及肿瘤微环境对这些活动的影响。我们还将讨论近期针对TAM进行靶向/破坏以及将其用作抗癌基因治疗载体的尝试。