Novel human STING activation by hydrated-prenylated xanthones from Garcinia cowa

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....

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Veröffentlicht in:Journal of pharmacy and pharmacology 2023-08, Vol.75 (8), p.1058-1065
Hauptverfasser: Tran, Thi Thu Thuy, Le, Phuong Mai, Nguyen, Thi Kim An, Hoang, Thi Minh Nguyet, Do, Thi Quynh An, Martel, Alexandrine L, Lewicky, Jordan D, Klem, Alexandra, Le, Hoang-Thanh
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Sprache:eng
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Zusammenfassung: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.
ISSN:0022-3573
2042-7158
DOI:10.1093/jpp/rgad038