Spatial transcriptomic analysis of tumour–immune cell interactions in melanoma arising from congenital melanocytic nevus

• Published in: Journal of the European Academy of Dermatology and Venereology 2024-08, Vol.38 (8), p.1599-1605
• Main Authors: Lim, Youngkyoung, Cho, Beom Keun, Kang, Seong‐Jun, Jeong, Soyoung, Kim, Hyun Je, Baek, Jiyoon, Moon, Ji Hwan, Lee, Cheol, Park, Chan‐Sik, Mun, Je‐Ho, Won, Chong Hyun, Park, Chung‐Gyu
• Format: Article
• Language: English
• Subjects: Axl Receptor Tyrosine Kinase; Blood Proteins; Cell Communication; Female; Galectin 3 - genetics; Galectin 3 - metabolism; Galectins - genetics; Galectins - metabolism; Gene Expression Profiling; Hepatitis A Virus Cellular Receptor 2 - genetics; Hepatitis A Virus Cellular Receptor 2 - metabolism; Humans; Lymphocytes, Tumor-Infiltrating - immunology; Macrophages - immunology; Macrophages - metabolism; Male; Melanoma - genetics; Melanoma - immunology; Melanoma - pathology; Middle Aged; Neoplasm Invasiveness; Nevus, Pigmented - genetics; Nevus, Pigmented - immunology; Nevus, Pigmented - metabolism; Nevus, Pigmented - pathology; Skin Neoplasms - genetics; Skin Neoplasms - immunology; Skin Neoplasms - pathology; T-Lymphocytes - immunology; Transcriptome
• ISSN: 0926-9959; 1468-3083; 1468-3083
• DOI: 10.1111/jdv.19881

Background Studies on the interaction between tumour‐infiltrating immune cells (TIICs) and tumour cells in melanoma arising from congenital melanocytic nevus (CMN) are lacking. Objective The aim of this study was to determine the intratumoral immune landscape of TIICs and tumour cells during invasion and metastasis. Methods Tissue specimens were obtained from patients with melanoma originating from CMN. Differential gene expression in melanoma cells and TIICs during invasion and metastasis was determined using spatial transcriptomics. Results As invasion depth increased, the expression of LGALS3, known to induce tumour‐driven immunosuppression, increased in melanoma cells. In T cells, the expression of genes that inhibit T‐cell activation increased with increasing invasion depth. In macrophages, the expression of genes related to the anti‐inflammatory M2 phenotype was upregulated with increasing invasion depth. Compared to primary tumour cells, melanoma cells in metastatic lesions showed upregulated expression of genes associated with cancer immune evasion, including AXL and EPHA2, which impede T‐cell recruitment, and BST2, associated with M2 polarization. Furthermore, T cells showed increased expression of genes related to immunosuppression, and macrophages exhibited increased expression of genes associated with the M2 phenotype. Conclusions The interaction between melanomas arising from CMN and TIICs may be important for tumour progression and metastasis.