Differential macrophage programming in the tumor microenvironment.

Differential macrophage programming in the tumor microenvironment.
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DOI:
10.1016/j.it.2011.12.001
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发表时间:
2012-03
影响因子:
16.8
通讯作者:
Coussens LM
Coussens LM
中科院分区:
医学1区
文献类型:
--
作者:
Ruffell B;Affara NI;Coussens LM

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在实体肿瘤中常见的多种独特的基质细胞类型中,肿瘤相关巨噬细胞(tam)已被认为对促进肿瘤进展具有重要意义。tam的肿瘤特性源于其调节血管生成程序的能力,为恶性细胞的增殖、存活和侵袭提供可溶性介质,并直接或间接抑制细胞毒性T细胞的活性。这些不同的活性依赖于tam的极化状态,部分受局部细胞因子和趋化因子浓度的调节,以及tam与细胞外基质正常和降解组分的各种相互作用。靶向调节TAM极化的分子通路在抗癌治疗中具有很大的前景。
Of the multiple unique stromal cell types common to solid tumors, tumor-associated macrophages (TAMs) have been recognized as significant for fostering tumor progression. The protumor properties of TAMs are derived from their ability to regulate angiogenic programming, provide soluble mediators to malignant cells for proliferation, survival and invasion, and for directly and indirectly suppressing activity of cytotoxic T cells. 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 anti-cancer therapy.
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