4.2 Article

Cytotoxic effects of Euterpe oleracea Mart. in malignant cell lines

Journal

Publisher

BIOMED CENTRAL LTD
DOI: 10.1186/1472-6882-14-175

Keywords

Anticancer; Euterpe oleracea mart.; MC Gamma-7; Phytochemicals; Chemopreventive

Funding

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq), Ministerio da Saude, Brasil
  2. Fundacao de Amparo a Pesquisa e ao Desenvolvimento Cientifico e Tecnologico do Estado do Maranhao (FAPEMA)

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Background: Euterpe oleracea Mart., a plant from the Amazon region, is commonly known as acai or jucara; it has high nutritional value and elevated levels of lipids, proteins, and minerals. Acai is an abundant and much consumed fruit by the Amazon local population, and studies have demonstrated that it is rich in phytochemicals with antioxidant, anti-inflammatory, and anticancer activities. Therefore, the aim of this study was to test this plant for anticancer activity in different human malignant cell lines. Methods: Cell lines derived from breast and colorectal adenocarcinomas were treated with 10, 20, and 40 mu g/mL of bark, seed, and total acai fruit hydroalcoholic extracts for 24 and 48 h. After treatment, cell viability was measured using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays, and cell morphological features were observed by light and transmission electron microscopy. The type of cell death was also evaluated. The data were analyzed statistically by one-way analysis of variance (ANOVA), followed by Dunnett's or Tukey's post hoc tests, as appropriate. Results: We observed that of all the cell lines tested, MCF-7 was the only line that responded to acai treatment. The extracts caused significant reduction (p < 0.01) in cell viability and altered cell morphological features by inducing the appearance of autophagic vacuoles, as observed by transmission electron microscopy. Furthermore, increased expression of LC3BII, a protein marker of autophagosome formation, was observed by western blotting. Caspase Glo (TM) assays and morphologic observations by DAPI nuclear staining and transmission electron microscopy did not indicate any apoptotic events. Conclusions: The present study demonstrated that acai possesses antitumorigenic potential in the MCF-7 cell line. Further studies are needed to identify the compound (s) responsible for this cytotoxic activity and the molecular target in the cell. This discovery of the anticancer potential of acai may help in the development of chemopreventive drugs and may have therapeutic effects in the treatment of breast cancer.

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