Plasticity beyond Cancer Cells and the "Immunosuppressive Switch"

被引:77
作者
Granot, Zvi [1 ]
Fridlender, Zvi G. [2 ]
机构
[1] Hebrew Univ Jerusalem, Inst Med Res Israel Canada, Dept Dev Biol & Canc Res, Sch Med, IL-91010 Jerusalem, Israel
[2] Hadassah Hebrew Univ, Med Ctr, Inst Pulm Med, Jerusalem, Israel
关键词
REGULATORY T-CELLS; TGF-BETA; MACROPHAGE ACTIVATION; ANGIOGENIC SWITCH; TUMOR PROGRESSION; DENDRITIC CELLS; FIBROBLASTS; DIFFERENTIATION; METASTASIS; MICROENVIRONMENT;
D O I
10.1158/0008-5472.CAN-15-1502
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor initiation, growth, and metastatic progression are complex processes that, in order to be successful, require extraordinary cellular plasticity. Accordingly, tumor cell plasticity and how it affects disease progression have been studied extensively. However, as our understanding of the tumor microenvironment deepens, we are confronted with the notion that functional plasticity in the context of cancer is not limited to tumor cells alone but is also commonly seen in normal stromal cells of the microenvironment, and specifically in immune cells. Here, we review the functional plasticity these cells exhibit in the context of cancer, highlighting the role of circulating and tumor-associated neutrophils. We further discuss how this plasticity supports or limits tumor progression, inducing an "immunosuppressive switch" to promote further tumor growth and development. (C) 2015 AACR.
引用
收藏
页码:4441 / 4445
页数:5
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