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Expression of LOXL3 , NES , and SNAI1 in Melanoma Genesis and Progression.
- Source :
-
Cells [Cells] 2024 Aug 29; Vol. 13 (17). Date of Electronic Publication: 2024 Aug 29. - Publication Year :
- 2024
-
Abstract
- Melanoma is the most severe type of skin cancer and among the most malignant neoplasms in humans. With the growing incidence of melanoma, increased numbers of therapeutic options, and the potential to target specific proteins, understanding the basic mechanisms underlying the disease's progression and resistance to treatment has never been more important. LOXL3, SNAI1, and NES are key factors in melanoma genesis, regulating tumor growth, metastasis, and cellular differentiation. In our study, we explored the potential role of LOXL3, SNAI1, and NES in melanoma progression and metastasis among patients with dysplastic nevi, melanoma in situ, and BRAF + and BRAF - metastatic melanoma, using immunofluorescence and qPCR analysis. Our results reveal a significant increase in LOXL3 expression and the highest NES expression in BRAF + melanoma compared to BRAF -, dysplastic nevi, and melanoma in situ. As for SNAI1, the highest expression was observed in the metastatic melanoma group, without significant differences among groups. We found co-expression of LOXL3 and SNAI1 in the perinuclear area of all investigated subgroups and NES and SNAI1 co-expression in melanoma cells. These findings suggest a codependence or collaboration between these markers in melanoma EMT, suggesting new potential therapeutic interventions to block the EMT cascade that could significantly affect survival in many melanoma patients.
- Subjects :
- Humans
Gene Expression Regulation, Neoplastic
Amino Acid Oxidoreductases genetics
Amino Acid Oxidoreductases metabolism
Skin Neoplasms genetics
Skin Neoplasms pathology
Skin Neoplasms metabolism
Cell Line, Tumor
Male
Female
Neoplasm Metastasis
Middle Aged
Melanoma genetics
Melanoma pathology
Melanoma metabolism
Snail Family Transcription Factors metabolism
Snail Family Transcription Factors genetics
Disease Progression
Subjects
Details
- Language :
- English
- ISSN :
- 2073-4409
- Volume :
- 13
- Issue :
- 17
- Database :
- MEDLINE
- Journal :
- Cells
- Publication Type :
- Academic Journal
- Accession number :
- 39273022
- Full Text :
- https://doi.org/10.3390/cells13171450