Proença Carina, Rufino Ana Teresa, Santos Isabela, Albuquerque Hélio M T, Silva Artur M S, Fernandes Eduarda, Ferreira de Oliveira José Miguel P
LAQV, REQUIMTE, Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
LAQV, REQUIMTE, Department of Chemistry, Campus Universitario de Santiago, University of Aveiro, 3810-193 Aveiro, Portugal.
Antioxidants (Basel). 2023 Sep 10;12(9):1744. doi: 10.3390/antiox12091744.
Osteosarcoma (OS) is a common childhood sarcoma, and its treatment is hindered by adverse effects, chemoresistance, and recurrence. Interleukin (IL)-6 production by tumors plays a significant role in inflammation, carcinogenesis, and metastasis. This study aimed to investigate the antiproliferative potential of luteolin derivatives in OS and to evaluate interleukin production. MG-63, Saos-2, HOS, and 143B human OS cell lines were incubated with luteolin and eight derivatives containing hydroxy, chlorine, or alkyl substitutions. The cell viability and growth were evaluated in the presence of these compounds. Apoptosis was also examined through the analysis of the Bax expression and caspase-3 activity. Finally, the gossypetin effects were measured regarding the production of proinflammatory cytokines interleukin (IL)-6, IL-1β, and IL-12p70. Our findings show that gossypetin was the most potent compound, with proliferation-suppressing activities that induced a series of critical events, including the inhibition of the cell viability and growth. Apoptosis was associated with enhanced caspase-3 activity and increased Bax expression, indicating the involvement of the intrinsic pathway of apoptosis. Moreover, pre-/co-treatment with gossypetin significantly reduced the autocrine production of proinflammatory cytokines. Further investigation is required; nevertheless, considering the link between inflammation, carcinogenesis, and metastasis in OS, our findings suggest that gossypetin exhibits anti-proliferative and anti-inflammatory properties that are potentially relevant in the clinical context.
骨肉瘤(OS)是一种常见的儿童肉瘤,其治疗受到副作用、化疗耐药性和复发的阻碍。肿瘤产生的白细胞介素(IL)-6在炎症、致癌作用和转移中起重要作用。本研究旨在探讨木犀草素衍生物在骨肉瘤中的抗增殖潜力,并评估白细胞介素的产生。将MG-63、Saos-2、HOS和143B人骨肉瘤细胞系与木犀草素及八种含有羟基、氯或烷基取代基的衍生物一起孵育。在这些化合物存在的情况下评估细胞活力和生长情况。还通过分析Bax表达和半胱天冬酶-3活性来检测细胞凋亡。最后,测定了棉黄素对促炎细胞因子白细胞介素(IL)-6、IL-1β和IL-12p70产生的影响。我们的研究结果表明,棉黄素是最有效的化合物,具有抑制增殖的活性,可诱导一系列关键事件,包括抑制细胞活力和生长。细胞凋亡与半胱天冬酶-3活性增强和Bax表达增加有关,表明细胞凋亡的内在途径参与其中。此外,棉黄素预处理/共处理可显著降低促炎细胞因子的自分泌产生。尽管还需要进一步研究,但考虑到骨肉瘤中炎症、致癌作用和转移之间的联系,我们的研究结果表明棉黄素具有抗增殖和抗炎特性,在临床环境中可能具有相关性。