Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Dec;35(12):1819-28.
doi: 10.1002/hed.23217. Epub 2013 Mar 6.

Focus on the role of the CXCL12/CXCR4 chemokine axis in head and neck squamous cell carcinoma

Affiliations
Review

Focus on the role of the CXCL12/CXCR4 chemokine axis in head and neck squamous cell carcinoma

Sébastien Albert et al. Head Neck. 2013 Dec.

Abstract

The human chemokine system includes approximately 48 chemokines and 19 chemokine receptors. The CXCL12/CXCR4 system is one of the most frequently studied that is also found overexpressed in a large variety of tumors. The CXCL12/CXCR4 axis has been increasingly identified as an important target in cancer growth, metastasis, relapse, and resistance to therapy. In this review, we highlight current knowledge of the molecular mechanisms involving chemokines CXCL12/CXCR4 and their consequences in head and neck squamous cell carcinoma (HNSCC). Overexpression of CXCL12/CXCR4 in HNSCC appears to activate cellular functions, including motility, invasion, and metastatic processes. Current findings suggest that CXCR4 and epithelial-mesenchymal transition markers are associated with tumor aggressiveness and a poor prognosis, and may be suitable biomarkers for head and neck tumors with high metastatic potential. Furthermore, knowledge of the role of CXCR4 in HNSCC could influence the development of new targeted therapies for treatment, aimed at improving the prognosis of this disease.

Keywords: SDF-1; epithelial-to-mesenchymal transition; head and neck cancer; hypoxia; invasion; metastasis.

PubMed Disclaimer

Publication types

MeSH terms

LinkOut - more resources