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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

(-)-Hinokinin Induces G2/M Arrest and Contributes to the Antiproliferative Effects of Doxorubicin in Breast Cancer Cells

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Author(s):
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Cunha, Nayanne Larissa [1] ; Teixeira, Gabriella Machado [1] ; Martins, Thomas Duzzi [1] ; Souza, Anderson Roberto [1] ; Oliveira, Pollyana Francieli [1] ; Smaro, Guilherme Venancio [1] ; Souza Rezende, Karen Cristina [1] ; Goncalves, Natalia dos Santos [1] ; Souza, Daniel Gottardo [1] ; Tavares, Denise Crispim [1] ; Andrade Silva, Marcio Lus [1] ; dos Santos, Raquel Alves [1]
Total Authors: 12
Affiliation:
[1] Univ Franca, Franca, SP - Brazil
Total Affiliations: 1
Document type: Journal article
Source: Planta Medica; v. 82, n. 6, p. 530-538, APR 2016.
Web of Science Citations: 4
Abstract

Breast cancer incidence rises worldwide and new chemotherapeutical strategies have been investigated to overcome chemoresistance. (-)-Hinokinin is a dibenzylbutyrolactone lignan derived from the partial synthesis of (-)-cubebin extracted from Piper cubeba seeds. Biological effects of dibenzylbutyrolactone lignans include antiviral, antitumor, anti-inflammatory, and trypanocidal activities. In the present study, we evaluated the ability of (-)-hinokinin to modulate the antiproliferative effects of doxorubicin intumoral (MCF-7 and SKBR-3) and normal (MCF-10A) breast cell lines. Treatment with (-)-hinokinin did not affect the cellular proliferation or contribute to the antitproliferative effects of doxorubicin in MCF-10A cells. After 24 and 48 hours of treatment with (-)-hinokinin, MCF-7 and SKBR-3 were accumulated in G2/M and, when combined with doxorubicin, (-)-hinokinin contributed to the antiproliferative effects of this chemotherapic by modulation of the cyclin-dependent kinase inhibitor 1. Apoptotic cell death was observed in response to (-)-hinokinin alone in MCF-7, but not in SKBR-3 even 72 hours after treatment. In MCF-7, doxorubicin-induced apoptosis was not increased by (-)-hinokinin. The findings of the present study suggest (-)-hinokinin as an antiproliferative agent that contributes to the effects of doxorubicin. (-)-Hinokinin modulates apoptotic cell death via the molecular regulation of the cell cycle and apoptotic control genes, but the cellular genetic background directly affects the cell fate decision in response to treatment. (AU)

FAPESP's process: 11/17935-7 - Assessment of the intracellular pathways modulated by rosmarinic acid and (-)-hinokinin in response to genotoxic stress
Grantee:Raquel Alves dos Santos
Support type: Regular Research Grants