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Curcumin Modulates Purinergic Signaling and Inflammatory Response in Cutaneous Metastatic Melanoma Cells

Abstract

Cutaneous melanoma (CM) poses a therapeutic challenge due to its aggressive nature and often limited response to conventional treatments. Exploring novel therapeutic targets is essential, and natural compounds have emerged as potential candidates. This study aimed to elucidate the impact of curcumin, a natural compound known for its anti-inflammatory, antioxidant, and anti-tumor properties, on metastatic melanoma cells, focusing on the purinergic system and immune responses. Human melanoma cell line SK-Mel-28 were exposed to different curcumin concentrations for either 6 or 24 h, after which we assessed components related to the purinergic system and the inflammatory cascade. Using RT-qPCR, we assessed the gene expression of CD39 and CD73 ectonucleotidases, as well as adenosine deaminase (ADA). Curcumin effectively downregulated CD39, CD73, and ADA gene expression. Flow cytometry analysis revealed that curcumin significantly reduced CD39 and CD73 protein expression at specific concentrations. Moreover, the A2A receptor's protein expression decreased across all concentrations. Enzymatic activity assays demonstrated that curcumin modulated CD39, CD73, and ADA activities, with effects dependent on concentration and duration of treatment. Extracellular ATP levels increased after 24 h of curcumin treatment, emphasizing its role in modulating hydrolytic activity. Curcumin also displayed anti-inflammatory properties by reducing NLRP3 gene expression and impacting the levels of key inflammatory cytokines. In conclusion, this study unveils the potential of curcumin as a promising adjuvant in CM treatment. Curcumin modulates the expression and activity of crucial components of the purinergic system and exhibits anti-inflammatory effects, indicating its potential therapeutic role in combating CM. These findings underscore curcumin's promise and warrant further investigation in preclinical and clinical settings for melanoma management.

Citing Articles

Therapeutic Significance of NLRP3 Inflammasome in Cancer: Friend or Foe?.

Jalali A, Mitchell K, Pompoco C, Poludasu S, Tran S, Ramana K Int J Mol Sci. 2025; 25(24.

PMID: 39769450 PMC: 11728390. DOI: 10.3390/ijms252413689.

References
1.
Arnold M, Singh D, Laversanne M, Vignat J, Vaccarella S, Meheus F . Global Burden of Cutaneous Melanoma in 2020 and Projections to 2040. JAMA Dermatol. 2022; 158(5):495-503. PMC: 8968696. DOI: 10.1001/jamadermatol.2022.0160. View

2.
Rebecca V, Somasundaram R, Herlyn M . Pre-clinical modeling of cutaneous melanoma. Nat Commun. 2020; 11(1):2858. PMC: 7275051. DOI: 10.1038/s41467-020-15546-9. View

3.
Gouravani M, Khalili N, Razi S, Keshavarz-Fathi M, Khalili N, Rezaei N . The NLRP3 inflammasome: a therapeutic target for inflammation-associated cancers. Expert Rev Clin Immunol. 2020; 16(2):175-187. DOI: 10.1080/1744666X.2020.1713755. View

4.
Di Virgilio F, Sarti A, Falzoni S, De Marchi E, Adinolfi E . Extracellular ATP and P2 purinergic signalling in the tumour microenvironment. Nat Rev Cancer. 2018; 18(10):601-618. DOI: 10.1038/s41568-018-0037-0. View

5.
Allard B, Longhi M, Robson S, Stagg J . The ectonucleotidases CD39 and CD73: Novel checkpoint inhibitor targets. Immunol Rev. 2017; 276(1):121-144. PMC: 5338647. DOI: 10.1111/imr.12528. View