Possible regulation of the immune modulator tetraspanin CD81 by alpha-synuclein in melanoma

We probed the mechanism by which the Parkinson's disease-associated protein α-synuclein (α-syn)/SNCA promotes the pathogenesis and progression of melanoma. We found that the human melanoma cell line SK-MEL-28 in which SNCA is knocked out (SNCA-KO) has low levels of tetraspanin CD81, which is a cell-surface protein that promotes invasion, migration, and immune suppression. Analyzing data from the Cancer Genome Atlas, we show that SNCA and CD81 mRNA levels are positively correlated in melanoma; melanoma survival is inversely related to the levels of SNCA and CD81; and SNCA/CD81 are inversely related to the expression of key cytokine genes (IL12A, IL12B, IFN, IFNG, PRF1 and GZMB) for immune activation and immune cell-mediated killing of melanoma cells. We propose that high levels of α-syn and CD81 in melanoma and in immune cells drive invasion and migration and in parallel cause an immunosuppressive microenvironment; these contributing factors lead to aggressive melanomas.

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Publication Details

Journal
Biochemical and Biophysical Research Communications
Published
2024-08-30
DOI
https://doi.org/10.1016/j.bbrc.2024.150631
Citations
6
Primary Topic
Cell Adhesion Molecules Research
Type
article
Field-Weighted Citation Impact
2.30

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article

Possible regulation of the immune modulator tetraspanin CD81 by alpha-synuclein in melanoma

Michael W. Graner, Christina Coughlan, Nirjhar M. Aloy, Stephan N. Witt
6 citations
Biochemical and Biophysical Research Communications
Cell Adhesion Molecules Research
2.30
article

Possible regulation of the immune modulator tetraspanin CD81 by alpha-synuclein in melanoma

Michael W. Graner, Christina Coughlan, Nirjhar M. Aloy, Stephan N. Witt
article en
6 citations

Abstract

We probed the mechanism by which the Parkinson's disease-associated protein α-synuclein (α-syn)/SNCA promotes the pathogenesis and progression of melanoma. We found that the human melanoma cell line SK-MEL-28 in which SNCA is knocked out (SNCA-KO) has low levels of tetraspanin CD81, which is a cell-surface protein that promotes invasion, migration, and immune suppression. Analyzing data from the Cancer Genome Atlas, we show that SNCA and CD81 mRNA levels are positively correlated in melanoma; melanoma survival is inversely related to the levels of SNCA and CD81; and SNCA/CD81 are inversely related to the expression of key cytokine genes (IL12A, IL12B, IFN, IFNG, PRF1 and GZMB) for immune activation and immune cell-mediated killing of melanoma cells. We propose that high levels of α-syn and CD81 in melanoma and in immune cells drive invasion and migration and in parallel cause an immunosuppressive microenvironment; these contributing factors lead to aggressive melanomas.

Biochemical and Biophysical Research CommunicationsVol. 734
University of Colorado Anschutz Medical Campus (US), Louisiana State University Health Sciences Center Shreveport (US)
Feist-Weiller Cancer Center
Zero hunger
Openalex Percentile: Top 11%
Cell Adhesion Molecules Research
2.30
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