(2020) CXCL-10: a new candidate for melanoma therapy? Cellular Oncology. pp. 353-365. ISSN 2211-3428
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Abstract
Background Melanoma is a malignancy that stems from melanocytes and is defined as the most dangerous skin malignancy in terms of metastasis and mortality rates. CXC motif chemokine 10 (CXCL10), also known as interferon gamma-induced protein-10 (IP-10), is a small cytokine-like protein secreted by a wide variety of cell types. CXCL10 is a ligand of the CXC chemokine receptor-3 (CXCR3) and is predominantly expressed by T helper cells (Th cells), cytotoxic T lymphocytes (CTLs), dendritic cells, macrophages, natural killer cells (NKs), as well as some epithelial and cancer cells. Similar to other chemokines, CXCL10 plays a role in immunomodulation, inflammation, hematopoiesis, chemotaxis and leukocyte trafficking. Conclusions Recent studies indicate that the CXCL10/CXCR3 axis may act as a double-edged sword in terms of pro- and anti-cancer activities in a variety of tissues and cells, especially in melanoma cells and their microenvironments. Most of these activities arise from the CXCR3 splice variants CXCR3-A, CXCR3-B and CXCR3-Alt. In this review, we discuss the pro- and anti-cancer properties of CXCL10 in various types of tissues and cells, particularly melanoma cells, including its potential as a therapeutic target.
Item Type: | Article |
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Keywords: | CXCL10 CXCR3 Melanoma Chemokine Cancer therapy Immunomodulation CHEMOKINE RECEPTOR CXCR3 MESENCHYMAL STEM-CELLS IFN-GAMMA INDUCIBLE PROTEIN-10 CHEMOATTRACTANT CYTOKINES ENDOTHELIAL-CELLS INTERFERON-GAMMA SPLICE VARIANT CXCL10 CANCER |
Subjects: | QZ Pathology > QZ 200-380 Neoplasms |
Divisions: | Faculty of Medicine > Departments of Clinical Sciences > Department of Pathology |
Page Range: | pp. 353-365 |
Journal or Publication Title: | Cellular Oncology |
Journal Index: | ISI |
Volume: | 43 |
Number: | 3 |
Identification Number: | https://doi.org/10.1007/s13402-020-00501-z |
ISSN: | 2211-3428 |
Depositing User: | Zahra Otroj |
URI: | http://eprints.mui.ac.ir/id/eprint/12261 |
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