Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/66880
Type: Artigo de periódico
Title: Ferruginol suppresses survival signaling pathways in androgen-independent human prostate cancer cells
Author: de Jesus, MB
Zambuzzi, WF
de Sousa, RRR
Areche, C
de Souza, ACS
Aoyama, H
Schmeda-Hirschmann, G
Rodriguez, JA
Brito, ARMD
Peppelenbosch, MP
den Hertog, J
de Paula, E
Ferreira, CV
Abstract: Ferruginol, a bioactive compound isolated from a Chilean tree (Podocarpaceae), attracts attention as a consequence of its pharmacological properties, which include anti-fungal, anti-bacterial, cardioprotective, anti-oxidative, anti-plasmodial and anti-ulcerogenic actions. Nevertheless, the molecular basis for these actions remains only partly understood and hence we investigated the effects of ferruginol on androgen-independent human prostate cancer cells (PC3), a known model for solid tumor cells with an exceptional resistance to therapy. The results show that ferruginol induces PC3 cell death via activation of caspases as well as apoptosis-inducing factor (AIF) as confirmed by its translocation into the nucleus. In order to clarify the biochemical mechanism responsible for the anti-tumor activity of ferruginol, we analyzed a set of molecular mediators involved in tumor cell survival, progression and aggressiveness. Ferruginol was able to trigger inhibition/downregulation of Ras/PI3K, STAT 3/5, protein tyrosine phosphatase and protein kinases related to cell cycle regulation. Importantly, the toxic effect of ferruginol was dramatically impeded in a more reducing environment, which indicates that at least in part, the anti-tumoral activity of ferruginol might be related to redox status modulation. This study supports further examination of ferruginol as a potential agent for both the prevention and treatment of prostate cancer. (C) 2008 Elsevier Masson SAS. All rights reserved.
Subject: natural compound
ferruginol
apoptosis
prostate cancer
Country: França
Editor: Elsevier France-editions Scientifiques Medicales Elsevier
Rights: fechado
Identifier DOI: 10.1016/j.biochi.2008.01.011
Date Issue: 2008
Appears in Collections:Unicamp - Artigos e Outros Documentos

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