DSE inhibits melanoma progression by regulating tumor immune cell infiltration and VCAN

• Published in: Cell death discovery Vol. 9; no. 1; pp. 373 - 10
• Main Authors: Xia, Lin, Feng, Maoxiao, Ren, Yidan, Hao, Xiaodong, Jiao, Qinlian, Xu, QinChen, Wang, Yunshan, Wang, Qin, Gong, Ningji
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 13.10.2023; Springer Nature B.V; Nature Publishing Group
• Subjects: 631/67/395; 631/67/580; 692/699/67; Apoptosis; Biochemistry; Biological activity; Biomedical and Life Sciences; Carcinogenesis; Cell Biology; Cell Cycle Analysis; Cell proliferation; Chondroitin sulfate; Epimerase; Flow cytometry; Infiltration; Life Sciences; Melanoma; Metastases; Proteomics; Stem Cells; Tumors
• ISSN: 2058-7716; 2058-7716
• DOI: 10.1038/s41420-023-01676-8

Dermatan sulfate epimerase (DSE) is a C5 epiminase that plays a key role in converting chondroitin sulfate into dermal sulfate. DSE is often upregulated during carcinogenesis of some types of cancer and can regulate growth factor signaling in cancer cells. However, the expression and function of DSE in human melanoma have not been reported. In this study, we investigated the influence of tumor-derived DSE in melanoma progression and the potential mechanism of their action. First, proteomic analysis of collected melanoma tissues revealed that DSE was significantly down-regulated in melanoma tissues. DSE silenced or overexpressed melanoma cells were constructed to detect the effect of DSE on melanoma cells, and it was found that the up-regulation of DSE significantly inhibited the proliferation, migration and invasion of melanoma cells. Data analysis and flow cytometry were used to evaluate the immune subpopulations in tumors, and it was found that the high expression of DSE was closely related to the invasion of killer immune cells. Mechanistically, DSE promoted the expression of VCAN, which inhibited the biological activity of melanoma cells. Together, these results suggest that DSE is downregulated in melanoma tissues, and that high expression of DSE can promote melanoma progression by inducing immune cell infiltration and VCAN expression.