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肿瘤微环境中的巨噬细胞差异化编程。

Differential macrophage programming in the tumor microenvironment.

机构信息

Department of Pathology, University of California, San Francisco, 513 Parnassus Ave, HSW450C, San Francisco, CA 94143, USA.

出版信息

Trends Immunol. 2012 Mar;33(3):119-26. doi: 10.1016/j.it.2011.12.001. Epub 2012 Jan 23.

Abstract

Of the multiple unique stromal cell types common to solid tumors, tumor-associated macrophages (TAMs) are significant for fostering tumor progression. The protumor properties of TAMs derive from regulation of angiogenic programming, production of soluble mediators that support proliferation, survival and invasion of malignant cells, and direct and indirect suppression of cytotoxic T cell activity. These varied activities are dependent on the polarization state of TAMs that is regulated in part by local concentrations of cytokines and chemokines, as well as varied interactions of TAMs with normal and degraded components of the extracellular matrix. Targeting molecular pathways regulating TAM polarization holds great promise for anticancer therapy.

摘要

在实体瘤中常见的多种独特基质细胞类型中,肿瘤相关巨噬细胞(TAMs)对促进肿瘤进展具有重要意义。TAMs 的促肿瘤特性源于对血管生成程序的调节、产生支持恶性细胞增殖、存活和侵袭的可溶性介质,以及直接和间接抑制细胞毒性 T 细胞活性。这些不同的活性取决于 TAMs 的极化状态,这种状态部分受到细胞因子和趋化因子的局部浓度以及 TAMs 与细胞外基质的正常和降解成分的不同相互作用的调节。靶向调节 TAM 极化的分子途径为癌症治疗带来了巨大的希望。

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