Immune evasion by murine melanoma mediated through CC chemokine receptor-10.
Human melanoma cells frequently express CC chemokine receptor (CCR)10, a receptor whose ligand (CCL27) is constitutively produced by keratinocytes. Compared with B16 murine melanoma, cells rendered more immunogenic via overexpression of luciferase, B16 cells that overexpressed both luciferase and CCR10 resisted host immune responses and readily formed tumors. In vitro, exposure of tumor cells to CCL27 led to rapid activation of Akt, resistance to cell death induced by melanoma antigen-specific cytotoxic T cells, and phosphatidylinositol-3-kinase (PI3K)-dependent protection from apoptosis induced by Fas cross-linking. In vivo, cutaneous injection of neutralizing antibodies to endogenous CCL27 blocked growth of CCR10-expressing melanoma cells. We propose that CCR10 engagement by locally produced CCL27 allows melanoma cells to escape host immune antitumor killing mechanisms (possibly through activation of PI3K/Akt), thereby providing a means for tumor progression.
Duke Scholars
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- Reverse Transcriptase Polymerase Chain Reaction
- Receptors, Chemokine
- Receptors, CCR10
- Mice, Inbred C57BL
- Mice
- Melanoma, Experimental
- Immunology
- Immunohistochemistry
- Humans
- Female
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Reverse Transcriptase Polymerase Chain Reaction
- Receptors, Chemokine
- Receptors, CCR10
- Mice, Inbred C57BL
- Mice
- Melanoma, Experimental
- Immunology
- Immunohistochemistry
- Humans
- Female