CXCR3, a double-edged sword in tumor progression and angiogenesis

被引:126
作者
Billottet, Clotilde
Quemener, Cathy
Bikfalvi, Andreas
机构
[1] INSERM, U1029, Talence, France
[2] Univ Bordeaux 1, F-33405 Talence, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2013年 / 1836卷 / 02期
关键词
CXCR3; CXC chemokines; Angiogenesis; Cancer; Tumor invasion; Tumor immunity; CHEMOKINE RECEPTOR CXCR3; PROTEIN-COUPLED RECEPTORS; AIRWAY EPITHELIAL-CELLS; X-C-CHEMOKINE; IFN-GAMMA; SMALL-MOLECULE; T-CELLS; PLATELET-FACTOR-4; VARIANT; DIFFERENTIAL EXPRESSION; INTERFERON-GAMMA;
D O I
10.1016/j.bbcan.2013.08.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CXC chemokines are involved in chemotaxis, regulation of cell growth, induction of apoptosis and modulation of angiostatic effects. CXCL9, CXCL10, CXCL11, CXCL4 and its variant CXCL4L1 are members of the CXC chemokine family, which bind to the CXCR3 receptor to exert their biological effects. These chemokines are associated with a variety of human diseases including chronic inflammation, immune dysfunction, cancer and metastasis. In this review, we focus on accumulating evidence demonstrating the pivotal role of CXCR3 in tumor progression. Its effects are mediated directly in tumor cells or indirectly through the regulation of angiogenesis and tumor immunity. Understanding the emerging role of CXCR3 and its signaling mechanisms further validates this receptor as a biomarker and therapeutic target for tumor progression and tumor angiogenesis. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:287 / 295
页数:9
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