The CXCL16-CXCR6 chemokine axis in glial tumors.

Abstract

Since chemokines and their receptors play a pivotal role in tumors, we investigated the CXCL16-CXCR6-axis in human astroglial tumors. The transmembrane chemokine CXCL16 is heavily expressed by tumor, microglial and endothelial cells in situ and in vitro. In contrast, the receptor CXCR6 is restricted in glioblastomas to a small subset of proliferating cells positive for the stem-cell markers Musashi, Nanog, Sox2 and Oct4. In particular, the vast majority (about 90%) of Musashi-positive cells stained also for CXCR6. Thus, CXCL16 is highly expressed by glial tumor and stroma cells whereas CXCR6 defines a subset of cells with stem cell character.

• Authors: Kirsten Hattermann, Janka Held-Feindt, Andreas Ludwig, Rolf Mentlein
• Journal: Journal of neuroimmunology (J Neuroimmunol) Vol. 260 Issue 1-2 Pg. 47-54 (Jul 15 2013) ISSN: 1872-8421 [Electronic] Netherlands
• PMID: 23628207 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2013 Elsevier B.V. All rights reserved.

Chemical References

• Biomarkers, Tumor
• CXCL16 protein, human
• CXCR6 protein, human
• Chemokine CXCL16
• Chemokines, CXC
• Homeodomain Proteins
• MSI1 protein, human
• NANOG protein, human
• Nanog Homeobox Protein
• Nerve Tissue Proteins
• Octamer Transcription Factor-3
• RNA, Messenger
• RNA-Binding Proteins
• Receptors, CXCR6
• Receptors, Chemokine
• Receptors, Scavenger
• Receptors, Virus
• SOX2 protein, human
• SOXB1 Transcription Factors

Topics

• Biomarkers, Tumor (genetics, metabolism)
• Brain Neoplasms (immunology, metabolism, pathology)
• Chemokine CXCL16
• Chemokines, CXC (genetics, immunology, metabolism)
• Glioblastoma (immunology, metabolism, pathology)
• Homeodomain Proteins (metabolism)
• Humans
• Nanog Homeobox Protein
• Neoplastic Cells, Circulating (metabolism)
• Neoplastic Stem Cells (immunology, metabolism)
• Nerve Tissue Proteins (metabolism)
• Neural Stem Cells (immunology, metabolism)
• Octamer Transcription Factor-3 (metabolism)
• Primary Cell Culture
• RNA, Messenger (metabolism)
• RNA-Binding Proteins (metabolism)
• Receptors, CXCR6
• Receptors, Chemokine (genetics, immunology, metabolism)
• Receptors, Scavenger (genetics, immunology, metabolism)
• Receptors, Virus (genetics, immunology, metabolism)
• SOXB1 Transcription Factors (metabolism)
• Stromal Cells (immunology, metabolism)
• Tumor Cells, Cultured