Tumor-derived CCL20 affects B16 melanoma growth in mice
Background - Chemokine ligand-20 (CCL20) expressed in the epidermis is a potent impetus for the recruitment of CC-chemokine receptor 6 (CCR6)-expressing subsets of DCs, B-cells and memory T-cells into the skin. CCL20 and CCR6+ immune cells have been detected in chronic inflammatory skin diseases and...
Gespeichert in:
| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2020
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| In: |
Journal of dermatological science
Year: 2019, Jahrgang: 97, Heft: 1, Pages: 57-65$79 |
| ISSN: | 1873-569X |
| DOI: | 10.1016/j.jdermsci.2019.12.005 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.jdermsci.2019.12.005 Verlag, lizenzpflichtig, Volltext: http://www.sciencedirect.com/science/article/pii/S0923181119303883 |
| Verfasserangaben: | Diego Martin-Garcia, Cinthia Silva-Vilches, Rainer Will, Alexander H. Enk, Anke S. Lonsdorf |
MARC
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| 245 | 1 | 0 | |a Tumor-derived CCL20 affects B16 melanoma growth in mice |c Diego Martin-Garcia, Cinthia Silva-Vilches, Rainer Will, Alexander H. Enk, Anke S. Lonsdorf |
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| 520 | |a Background - Chemokine ligand-20 (CCL20) expressed in the epidermis is a potent impetus for the recruitment of CC-chemokine receptor 6 (CCR6)-expressing subsets of DCs, B-cells and memory T-cells into the skin. CCL20 and CCR6+ immune cells have been detected in chronic inflammatory skin diseases and several malignancies, including melanoma. Yet, the functional contribution of the CCR6/CCL20 axis for melanoma progression remains controversial. - Objective - The functional contribution of CCR6-expressing immune cell subsets and local CCL20 in the tumor microenvironment for the immune control of melanoma was studied. - Methods - Homeostatic and inducible CCL20 secretion of murine (B16, Ret) and human (A375, C32) melanoma cells was analyzed by ELISA. To assess the functional relevance of CCR6/CCL20 interactions on local tumor progression, prestimulated or retrovirally transduced B16/F1 melanoma cells overexpressing CCL20 (B16-CCL20) were injected subcutaneously into C57BL/6 Wt mice and congenic CCR6-deficient (CCR6−/−) mice. Infiltrating leucocytes were examined by flow cytometry in tumors and draining lymph nodes (DLNs). - Results - Melanoma cell lines up-regulate CCL20 secretion upon stimulation with pro-inflammatory cytokines in vitro. While only moderate changes in phenotype and composition of leucocytes were detected in advanced tumors and DLNs, mice injected with CCR6+ B16-CCL20 cells developed smaller tumors compared to B16-Control injected littermates, with CCR6-/- mice displaying the most pronounced reduction in tumor growth and incidence. - Conclusion - Our results suggest that CCR6/CCL20 interactions and individual independent effects of CCL20 and CCR6 in the microenvironment may be essential for melanoma progression and suggest a decisive role of this chemokine axis for melanoma pathogenesis beyond chemoattraction. | ||
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| 650 | 4 | |a CCL20 | |
| 650 | 4 | |a CCR6 | |
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| 650 | 4 | |a Melanoma | |
| 650 | 4 | |a Tumor infiltrating leucocytes | |
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