Support of Tumor Endothelial Cells by Chemokine Receptors

被引:50
作者
Salazar, Nicole [1 ]
Zabel, Brian A. [2 ]
机构
[1] San Francisco State Univ, Dept Biol, San Francisco, CA 94132 USA
[2] Vet Affairs Palo Alto Hlth Care Syst, Palo Alto Vet Inst Res, Palo Alto, CA 94304 USA
关键词
chemokine receptor; chemoattractant; endothelial cell; tumor vasculature; tumor microenvironment; TRANSENDOTHELIAL MIGRATION; PROGENITOR CELLS; I-TAC; CXCR7; ANGIOGENESIS; EXPRESSION; GROWTH; AXIS; STEM; METASTASIS;
D O I
10.3389/fimmu.2019.00147
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor-associated vascular endothelium comprises a specialized and diverse group of endothelial cells that, although not cancer themselves, are integral to cancer progression. Targeting the tumor vasculature can have significant efficacy in reducing tumor burden, although loss of efficacy due to acquisition of resistance mechanisms is common. Here we review mechanisms by which tumor endothelial cells (TEC) utilize chemokine receptors to support tumor progression. We illustrate how chemokine receptors support and may serve as functional markers of the diverse TEC population. We focus on ACKR1 (DARC), ACKR3 (CXCR7), CXCR4, and CCR2, as these are the best studied chemokine receptors in TEC: and suggest that targeting these receptors on the tumor vasculature may prove efficacious in slowing or reversing tumor growth. We also mention CXCR2 and CXCR3 as important mediators or tumor angiogenesis, given their distinct roles with angiogenic and angiostatic chemokines, respectively.
引用
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页数:9
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