Email updates

Keep up to date with the latest news and content from BMC Proceedings and BioMed Central.

This article is part of the supplement: São Paulo Advanced School of Comparative Oncology: Abstracts

Open Access Poster presentation

Lafoensia pacari extract induces apoptosis mediated by caspase-3 and inhibition of growth in human lung cancer cells

Yonara G Cordeiro1, Arina L Rochetti1, Antônio M Scatolini1, Edson R Silva1, Vinicius C Souza2 and Heidge Fukumasu1*

Author affiliations

1 Department of Basic Science, FZEA, University of Sao Paulo, Pirassununga, Brazil

2 Department of Biological Science, ESALQ, University of Sao Paulo, Piracicaba, Brazil

For all author emails, please log on.

Citation and License

BMC Proceedings 2013, 7(Suppl 2):P70  doi:10.1186/1753-6561-7-S2-P70


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/7/S2/P70


Published:4 April 2013

© 2013 Cordeiro et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Background

Lafoensia pacari is a native species from South America which has been used in traditional medicine as anti-ulcerogenic and anti-inflammatory for several diseases, but the antineoplastic potential still have not been elucidated so far, though its etnopharmacological indication. The aim of this study was to evaluate the anti-neoplastic effect of L. pacari ethanolic extract in three human lung neoplastic cell lines.

Materials and methods

For the assessment of cytotoxicity, cell lines were grown in vitro, being two originally from non-small cell lung carcinoma (A549 and H2023) and one of giant cell lung carcinoma obtained from pleural effusion (H460). Cells were grown in 96 well plates under regular cell culture condition and treated with different concentrations of L.pacari ethanolic extract, then analyzed using 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyl bromide tetrazolium, widely used to determine the viability of cultured cells. The IC50 value and the regression curve were calculated with 5.0 Prism (GraphPad Software, USA). Also, the Caspase-3 Assay Kit for Live Cells (Biotium, USA) was used to determine the mode of action of L. pacari at IC50 concentration.

Results

After the treatment for 72h with the ethanolic extract of L.pacari, we determined a dose-dependent effect of L. pacari extract in all cell lineages, being the H460 cell line the most sensitive by means of lowest IC50. Thus, we also showed that this effect was due to induced caspase-3 dependent apoptosis.

Conclusions

The extract of L. pacari demonstrated an antineoplastic effect in all cell lines. The Caspase-3 activation in tumor cells after treatment with L. pacari suggests that the cytotoxic effect is related to activation of the intrinsic apoptotic pathway, leading ultimately to cell death. Further studies are under investigation to determine the specific substances responsible for these effects.

Financial support

CAPES and FAPESP (2008/56584-2).