Department of Biochemistry and Molecular Biology, Louisiana State University Health Sciences Center, Shreveport, LA, USA; Feist-Weiller Cancer Center, Louisiana State University Health Shreveport, Shreveport, USA.
University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Biochem Biophys Res Commun. 2024 Nov 19;734:150631. doi: 10.1016/j.bbrc.2024.150631. Epub 2024 Aug 30.
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.
我们探究了帕金森病相关蛋白α-突触核蛋白(α-syn)/SNCA 促进黑色素瘤发病和进展的机制。我们发现,SNCA 敲除(SNCA-KO)的人黑色素瘤细胞系 SK-MEL-28 中,四跨膜蛋白 CD81 水平较低,CD81 是一种促进侵袭、迁移和免疫抑制的细胞表面蛋白。分析癌症基因组图谱的数据,我们表明黑色素瘤中 SNCA 和 CD81 mRNA 水平呈正相关;黑色素瘤的存活率与 SNCA 和 CD81 水平呈负相关;SNCA/CD81 与关键细胞因子基因(IL12A、IL12B、IFN、IFNG、PRF1 和 GZMB)的表达呈负相关,这些基因参与免疫激活和免疫细胞介导的黑色素瘤细胞杀伤。我们提出,黑色素瘤和免疫细胞中高水平的α-syn 和 CD81 驱动侵袭和迁移,并平行导致免疫抑制微环境;这些促成因素导致侵袭性黑色素瘤。