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CXCL12 / CXCR4 / CXCR7 chemokine axis and cancer progression

Authors :
Guangcun Cheng
Jianghua Zheng
Kenneth J. Pienta
Russell S. Taichman
Mingang Hao
Xiaoming Zhou
Xueqing Sun
Jian Zhang
Jianhua Wang
Source :
Cancer and Metastasis Reviews. 29:709-722
Publication Year :
2010
Publisher :
Springer Science and Business Media LLC, 2010.

Abstract

Chemokines, small pro-inflammatory chemoattractant cytokines that bind to specific G-protein coupled seven-span transmembrane receptors (GPCRs), are major regulators of cell trafficking and adhesion. The chemokine CXCL12 [also called stromal-derived factor-1 (SDF-1)] is an important α-chemokine that binds primarily to its cognate receptor CXCR4 and thus regulates the trafficking of normal and malignant cells. For many years it was believed that CXCR4 was the only receptor for CXCL12. Yet recent work has demonstrated that CXCL12 also binds to another seven-transmembrane span receptor called CXCR7. Our group and others have established critical roles for CXCR4 and CXCR7 on mediating tumor metastasis in several types of cancers, in addition to their contributions as biomarkers of tumor behavior as well as potential therapeutic targets. Here we review the current concepts regarding the role of CXCL12/CXCR4/CXCR7 axis activation, which regulates the pattern of tumor growth and metastatic spread to organs expressing high levels of CXCL12 to develop secondary tumors. We also summarize recent therapeutic approaches to target these receptors and/or their ligands.

Details

ISSN :
15737233 and 01677659
Volume :
29
Database :
OpenAIRE
Journal :
Cancer and Metastasis Reviews
Accession number :
edsair.doi.dedup.....6fd335f7abd0ec370611a4512e53c559