黄原酮
磺酰罗丹明B细胞培养试剂染料
预酸化
干扰素
细胞培养
肿瘤坏死因子α
IC50型
细胞因子
药理学
化学
生物
分子生物学
生物化学
体外
细胞毒性
酶
免疫学
立体化学
遗传学
作者
Thi Thu Thuy Tran,Phuong Mai Le,Thi Kim An Nguyen,Thi Minh Nguyet Hoang,Taeha An,Alexandrine L. Martel,Jordan D. Lewicky,Alexandra Klem,Hoang‐Thanh Le
摘要
Abstract Objectives We investigate the anticancer activity and human stimulator of interferon genes pathway activation by a new hydrated-prenylated tetraoxygenated xanthone, garcicowanone I (1) and two known xanthones (2 and 3) that were isolated from the root bark of Garcinia cowa Roxb. ex Choisy. Methods The anticancer activity of each compound was evaluated by sulforhodamine B assay in immortalized cancer cell lines. Stimulator of interferon genes pathway activation was assessed by western blot analysis using human THP-1-derived macrophages. The production of pro-inflammatory cytokines from these macrophages was also evaluated via enzyme-linked immunosorbent assay. Key findings Both compounds 1 and 3 displayed moderate inhibitory effects on the cancer cells, including a cisplatin-resistant cell line, with IC50 values in the range of 10–20 µM. All three xanthones activated the stimulator of interferon genes, as evidenced by phosphorylation of tank-binding kinase 1, the stimulator of interferon genes protein and interferon regulatory factor 3. Furthermore, treatment of these macrophages with compounds 1–3 led to the production of pro-inflammatory cytokines, including interleukin 6, tumour necrosis factor α and interleukin 1β. Conclusions In conclusion, the isolated xanthones, including the novel garcicowanone I, displayed promising anticancer and immunomodulatory activity that warrants further research.
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