趋化因子受体
趋化因子受体
血管生成
CCR2型
趋化因子
CXCR3型
癌症研究
CCR10
肿瘤进展
受体
CCR3
免疫学
CXCL1型
医学
肿瘤微环境
CXCR4型
生物
癌症
肿瘤细胞
内科学
作者
Nicole Salazar,Brian A. Zabel
标识
DOI:10.3389/fimmu.2019.00147
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.
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