The Brazilian octocoral Phyllogorgia dilatata as a source of cytotoxic compounds

The extensive marine biodiversity has proved to be a promising source of substances with biomedical potential. In this study, the cytotoxicity of the Brazilian octocoral Phyllogorgia dilatata (Gorgoniidae) was evaluated against two tumor cell lines and three bacterial strains. The methanol/dichlorom...

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Veröffentlicht in:Anais da Academia Brasileira de Ciências 2021-01, Vol.93 (4), p.e20200686-e20200686, Article 20200686
Hauptverfasser: Fagundes, Thayssa S. F., Macedo, Arthur L., Rigato, Dhiego B., Do Amaral, Bruno S., Jimenez, Paula Christine, Costa-Lotufo, Leticia, Pereira, Renata F. A., Aguiar-Alves, Fabio, Soares, Angelica R., Vasconcelos, Thatyana R. A., Cass, Quezia B., Valverde, Alessandra L.
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Sprache:eng
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Zusammenfassung:The extensive marine biodiversity has proved to be a promising source of substances with biomedical potential. In this study, the cytotoxicity of the Brazilian octocoral Phyllogorgia dilatata (Gorgoniidae) was evaluated against two tumor cell lines and three bacterial strains. The methanol/dichloromethane crude extract presented no antibacterial activity up to the highest concentration tested (512 mu g/mL), however it revealed a noteworthy antiproliferative effect against HCT-116 (80%) and MCF-7 (54%) cell lines at 50 mu g/mL. Therefore, guided by the cytotoxic activity, a multistep chemical fractionation of the extract provided the subfraction 5 (PDPH2-5) with IC 50 values of 3.18 and 17.80 mu g/mL against HCT-116 and MCF-7, respectively. The LC-HRMS/MS analysis of PDPH2-5 showed ions of m/z 219.1742 and 219.1743, characterized as (E,E) and (Z,E) germacrone, after a LC-DAD-SPE/NMR analysis of the hexanic fraction and comparisons of NMR data with the literature. Previously reported assessments to the cytotoxic activity of the (E,E)-diastereoisomer disclosed higher IC 50 values than that obtained for the PDPH2-5 fraction, suggesting, herein, a potentiated effect of the diastereoisomeric mixture. Such remark encourage further bioactivity studies with stereoisomer mixtures and reduce the urge for compound isolation.
ISSN:0001-3765
1678-2690
1678-2690
DOI:10.1590/0001-3765202120200686