Pharmacological properties and therapeutic potential of saffron (Crocus sativus L.) in osteosarcoma

Abstract Objectives In this comprehensive study, we aimed to investigate pharmacological properties and therapeutic significance of saffron in osteosarcoma cancer cells. Methods Plant materials were obtained from Safranbolu district of Karabuk, Turkey. For the determination of anticancer properties,...

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Veröffentlicht in:Journal of pharmacy and pharmacology 2020-01, Vol.72 (1), p.56-67
Hauptverfasser: Ege, Bilal, Yumrutas, Onder, Ege, Miray, Pehlivan, Mustafa, Bozgeyik, Ibrahim
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Sprache:eng
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Zusammenfassung:Abstract Objectives In this comprehensive study, we aimed to investigate pharmacological properties and therapeutic significance of saffron in osteosarcoma cancer cells. Methods Plant materials were obtained from Safranbolu district of Karabuk, Turkey. For the determination of anticancer properties, thiazolyl blue tetrazolium bromide (MTT) cell viability, colony formation, wound closure, DNA ladder assays and gene expression analysis by real-time PCR were performed. Also, cellular inflammation, total antioxidant and oxidants status were determined. Key findings Dichloromethane and hexane extracts of saffron were significantly inhibited cell proliferation and interfered with colony forming and migration capabilities of U2-OS osteosarcoma cancer cells. Also, both extracts induced the activation of tumour suppressor CDKN2B gene and altered cellular morphology resembling the induction of apoptosis. However, DNA fragmentation was not observed after extract treatments. Saffron was also found to have no significant effect on cellular inflammation. Unexpectedly, both dichloromethane and hexane extracts of saffron had no marked effect on cellular total antioxidant and oxidant status. Lastly, vanillic acid, resveratrol, caffeic acid and 4-hydroxybenzoic acid were found to be highly rich in our extracts. Conclusions Findings of this study demonstrated significant antiproliferative and antitumorigenic properties of saffron in osteosarcoma.
ISSN:0022-3573
2042-7158
DOI:10.1111/jphp.13179