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Provedor de dados:  ArchiMer
País:  France
Título:  Antiproliferative Activity of Violaxanthin Isolated from Bioguided Fractionation of Dunaliella tertiolecta Extracts
Autores:  Pasquet, Virginie
Morisset, Perrine
Ihammouine, Said
Chepied, Amandine
Aumailley, Lucie
Berard, Jean-baptiste
Serive, Benoit
Kaas, Raymond
Lanneluc, Isabelle
Thiery, Valerie
Lafferriere, Mathieu
Piot, Jean-marie
Patrice, Thierry
Cadoret, Jean-paul
Picot, Laurent
Data:  2011-05
Ano:  2011
Palavras-chave:  Pigments
Microalgae
Dunaliella
Violaxanthin
Carotenoid
Cancer
Apoptosis
Resumo:  Dunaliella tertiolecta (DT) was chemically investigated to isolate molecules inhibiting cancer cell proliferation and inducing apoptosis in vitro. The potency to inhibit cell growth was used for the bio-guided fractionation and isolation of active compounds using chromatographic techniques. The DT dichloromethane extract exhibited a strong anti-proliferative activity on MCF-7 and LNCaP cells, and was further fractionated and sub-fractionated by RP-HPLC. High resolution mass spectrometry and spectrophotometric analysis unequivocally identified violaxanthin as the most antiproliferative molecule present in DT DCM extract. Violaxanthin purified from DT induced MCF-7 dose- dependent growth inhibition in continuous and discontinuous treatments, at concentrations as low as 0.1 mu g.mL(-1) (0.17 mu M). Phosphatidylserine exposure, typical of early apoptosis, was observed after 48 h treatment at 8 mu g.mL(-1) (13.3 mu M) but no DNA fragmentation, characteristic of late apoptosis steps, could be detected even after 72 h treatment at 40 mu g.mL(-1) (66.7 mu M). Taken together, our results demonstrate the strong antiproliferative activity of violaxanthin on one human mammary cancer cell line, and suggest that studying the pharmacology of violaxanthin and pharmacomodulated derivatives on cancer cells may allow potent antiproliferative drugs to be obtained.
Tipo:  Text
Idioma:  Inglês
Identificador:  http://archimer.ifremer.fr/doc/00040/15142/12575.pdf

DOI:10.3390/md9050819
Editor:  Mdpi Ag
Relação:  http://archimer.ifremer.fr/doc/00040/15142/
Formato:  application/pdf
Fonte:  Marine Drugs (1660-3397) (Mdpi Ag), 2011-05 , Vol. 9 , N. 5 , P. 819-831
Direitos:  2011 MDPI Publishing
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