dc.creator | Bomfim, Diogo S. | |
dc.creator | Ferraz, Rosana Paula Cruz | |
dc.creator | Carvalho, Nanashara Coelho de | |
dc.creator | Soares, Milena Botelho Pereira | |
dc.creator | Pinheiro, Maria Lúcia Bélem | |
dc.creator | Costa, Emmanoel Vilaça | |
dc.creator | Bezerra, Daniel Pereira | |
dc.date | 2014-10-09T14:02:22Z | |
dc.date | 2014-10-09T14:02:22Z | |
dc.date | 2013 | |
dc.date.accessioned | 2023-09-26T20:42:02Z | |
dc.date.available | 2023-09-26T20:42:02Z | |
dc.identifier | BOMFIM, Diogo D. et al. Eudesmol isomers induce caspase-mediated apoptosis in human hepatocellular carcinoma HepG2 cells. Basic & Clinical Pharmacology & Toxicology, v. 113, n. 5, p. 300-306, 2013. | |
dc.identifier | 1742-7843 | |
dc.identifier | https://www.arca.fiocruz.br/handle/icict/8565 | |
dc.identifier | 10.1111/bcpt.12097 | |
dc.identifier.uri | https://repositorioslatinoamericanos.uchile.cl/handle/2250/8862272 | |
dc.description | Eudesmols are naturally occurring sesquiterpenoid alcohols that present cytotoxic effect to cancer cells. Herein, all eudesmol isomers displayed cytotoxicity to different tumour cell lines. a-Eudesmol showed IC50 values ranging from 5.38 1.10 to 10.60 1.33 lg/mL for B16-F10 and K562 cell lines, b-eudesmol showed IC50 values ranging from 16.51 1.21 to 24.57 2.75 lg/mL for B16-F10 and HepG2 cell lines, and c-eudesmol showed IC50 values ranging from 8.86 1.27 to 15.15 1.06 lg/mL for B16-F10 and K562 cell lines, respectively. In addition, in this work, we studied the mechanisms of cytotoxic action of eudesmol isomers (a-, b- and c-eudesmol) in human hepatocellular carcinoma HepG2 cells. After 24-hr incubation, HepG2 cells treated with eudesmol isomers presented typical hallmarks of apoptosis, as observed by morphological analysis in cells stained with haematoxylin–eosin and acridine orange/ethidium bromide. None of eudesmol isomers caused membrane disruption at any concentration tested. Moreover, eudesmol isomers induced loss of mitochondrial membrane potential and an increase in caspase-3 activation in HepG2 cells, suggesting the induction of caspase-mediated apoptotic cell death. In conclusion, the eudesmol isomers herein investigated are able to reduce cell proliferation and to induce tumour cell death by caspase-mediated apoptosis pathways. | |
dc.format | application/pdf | |
dc.language | eng | |
dc.publisher | John Wiley & Sons Ltd | |
dc.rights | open access | |
dc.subject | Eudesmol Isomers | |
dc.subject | Human Hepatocellular | |
dc.subject | Carcinoma HepG2 Cells | |
dc.subject | Apoptose/efeitos de drogas | |
dc.subject | Sesquiterpenos de Eudesmano/farmacologia | |
dc.subject | Carcinoma Hepatocelular/metabolismo | |
dc.subject | Carcinoma Hepatocelular/patologia | |
dc.subject | Caspase 3/genética | |
dc.subject | Caspase 3/metabolismo | |
dc.subject | Linhagem Celular Tumoral | |
dc.subject | Membrana Celular/efeitos de drogas | |
dc.subject | Proliferação de Células/efeitos de drogas | |
dc.subject | Células Hep G2 | |
dc.subject | Humanos | |
dc.subject | Concentração Inibidora 50 | |
dc.subject | Células K562 | |
dc.subject | Potencial da Membrana Mitocondrial/efeitos de drogas | |
dc.title | Eudesmol isomers induce caspase-mediated apoptosis in human hepatocellular carcinoma HepG2 cells | |
dc.type | Article | |