Manica Daiane, da Silva Gilnei Bruno, Narzetti Rafael Antônio, Dallagnoll Paula, da Silva Alana Patrícia, Marafon Filomena, Cassol Joana, de Souza Matias Letícia, Zamoner Ariane, de Oliveira Maciel Sarah Franco Vieira, Moreno Marcelo, Bagatini Margarete Dulce
Department of Biochemistry, Biochemistry Graduate Program, Federal University of Santa Catarina, Florianopolis, SC, Brazil.
Multicentric Graduate Program in Biochemistry and Molecular Biology, State University of Santa Catarina, Lages, SC, Brazil.
Purinergic Signal. 2025 Apr;21(2):277-288. doi: 10.1007/s11302-024-10023-0. Epub 2024 May 27.
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.
皮肤黑色素瘤(CM)因其侵袭性本质以及对传统治疗的反应往往有限,给治疗带来了挑战。探索新的治疗靶点至关重要,天然化合物已成为潜在的候选物。本研究旨在阐明姜黄素(一种以其抗炎、抗氧化和抗肿瘤特性而闻名的天然化合物)对转移性黑色素瘤细胞的影响,重点关注嘌呤能系统和免疫反应。将人黑色素瘤细胞系SK-Mel-28暴露于不同浓度的姜黄素中6小时或24小时,之后我们评估了与嘌呤能系统和炎症级联相关的成分。使用逆转录定量聚合酶链反应(RT-qPCR),我们评估了CD39和CD73外核苷酸酶以及腺苷脱氨酶(ADA)的基因表达。姜黄素有效地下调了CD39、CD73和ADA的基因表达。流式细胞术分析显示,姜黄素在特定浓度下显著降低了CD39和CD73的蛋白表达。此外,A2A受体的蛋白表达在所有浓度下均下降。酶活性测定表明,姜黄素调节了CD39、CD73和ADA的活性,其作用取决于治疗浓度和持续时间。姜黄素处理24小时后细胞外ATP水平升高,强调了其在调节水解活性中的作用。姜黄素还通过降低NLRP3基因表达和影响关键炎症细胞因子水平表现出抗炎特性。总之,本研究揭示了姜黄素作为CM治疗中有前景的佐剂的潜力。姜黄素调节嘌呤能系统关键成分的表达和活性,并表现出抗炎作用,表明其在对抗CM中的潜在治疗作用。这些发现强调了姜黄素的前景,并值得在黑色素瘤管理的临床前和临床环境中进行进一步研究。