姜黄素调节皮肤转移性黑色素瘤细胞的嘌呤能信号转导和炎症反应

IF 3 4区 医学 Q2 NEUROSCIENCES
Daiane Manica, Gilnei Bruno da Silva, Rafael Antônio Narzetti, Paula Dallagnoll, Alana Patrícia da Silva, Filomena Marafon, Joana Cassol, Letícia de Souza Matias, Ariane Zamoner, Sarah Franco Vieira de Oliveira Maciel, Marcelo Moreno, Margarete Dulce Bagatini
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引用次数: 0

摘要

皮肤黑色素瘤(CM)具有侵袭性,对传统疗法的反应往往有限,因此给治疗带来了挑战。探索新的治疗靶点至关重要,而天然化合物已成为潜在的候选靶点。姜黄素是一种以抗炎、抗氧化和抗肿瘤特性著称的天然化合物,本研究旨在阐明姜黄素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。将人类黑色素瘤细胞株 SK-Mel-28 暴露于不同浓度的姜黄素 6 或 24 小时后,我们评估了与嘌呤能系统和炎症级联相关的成分。我们使用 RT-qPCR 评估了 CD39 和 CD73 外切核苷酸酶以及腺苷脱氨酶(ADA)的基因表达。姜黄素能有效下调 CD39、CD73 和 ADA 基因的表达。流式细胞术分析表明,姜黄素在特定浓度下可显著降低 CD39 和 CD73 蛋白表达。此外,A2A受体的蛋白表达在所有浓度下都有所下降。酶活性测定表明,姜黄素能调节 CD39、CD73 和 ADA 的活性,其效果取决于浓度和治疗时间。姜黄素处理 24 小时后,细胞外 ATP 水平升高,强调了姜黄素在调节水解活性方面的作用。姜黄素还通过减少 NLRP3 基因的表达和影响关键炎症细胞因子的水平而显示出抗炎特性。总之,本研究揭示了姜黄素作为一种有前景的辅助药物治疗中风的潜力。姜黄素能调节嘌呤能系统关键成分的表达和活性,并具有抗炎作用,这表明姜黄素具有抗击 CM 的潜在治疗作用。这些研究结果突显了姜黄素的前景,值得在临床前和临床环境中进一步研究它对黑色素瘤的治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Curcumin modulates purinergic signaling and inflammatory response in cutaneous metastatic melanoma cells.

Curcumin modulates purinergic signaling and inflammatory response in cutaneous metastatic melanoma cells.

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.

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来源期刊
Purinergic Signalling
Purinergic Signalling 医学-神经科学
CiteScore
6.60
自引率
17.10%
发文量
75
审稿时长
6-12 weeks
期刊介绍: Nucleotides and nucleosides are primitive biological molecules that were utilized early in evolution both as intracellular energy sources and as extracellular signalling molecules. ATP was first identified as a neurotransmitter and later as a co-transmitter with all the established neurotransmitters in both peripheral and central nervous systems. Four subtypes of P1 (adenosine) receptors, 7 subtypes of P2X ion channel receptors and 8 subtypes of P2Y G protein-coupled receptors have currently been identified. Since P2 receptors were first cloned in the early 1990’s, there is clear evidence for the widespread distribution of both P1 and P2 receptor subtypes in neuronal and non-neuronal cells, including glial, immune, bone, muscle, endothelial, epithelial and endocrine cells.
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