Maytenus ilicifolia dry extract protects normal cells, induces apoptosis and regulates Bcl-2 in human cancer cells

Author:

Júnior Raimundo Fernandes de Araújo12,Oliveira Ana Luiza Cabral de Sá Leitão3,Pessoa Jonas Bispo1,Garcia Vinícios Barreto1,Guerra Gerlane Coelho Bernardo4,Soares Luiz Alberto Lira5,de Souza Tatiane Pereira6,Petrovick Pedro Ros7,de Araújo Aurigena Antunes348

Affiliation:

1. Departament of Morphology, Federal University of Rio Grande do Norte, Natal, Cep: 59078-970, Brazil

2. Post graduation program in Functional and Structural Biology/ Post graduation program Health Science/Department of Morphology, UFRN , Natal, Cep: 59078-970, Brazil

3. Programm post-graduation Pharmaceutical Science Federal University of Rio Grande do Norte, Natal, Cep: 59078-970, Brazil

4. Departament of Biophysic and Pharmacology, Federal University of Rio Grande do Norte, Natal, Cep: 59078-970, Brazil

5. Departament of Pharmaceutical Sciences /Federal University of Pernambuco, Recife, Cep: 50740-530, Brazil

6. Departament of Drugs and Foods/Federal University of Amazonas, Manaus, Cep:69010-300, Brazil

7. Faculty of Pharmacy / Federal University of do Rio Grande do Sul, Porto Alegre, Cep: 90610-000, Brazil

8. Post graduation program Public Health UFRN, Natal, Cep: 59078-970, Brazil

Abstract

Maytenus is the largest genus of the family Celastraceae and the species Maytenus ilicifolia (popularly known as ‘Espinheira Santa’). It is widely used in traditional Brazilian medicine to treat stomach conditions including nausea, gastritis, and ulcers. In this study, the apoptotic effects of a spray-dried extract of M. ilicifolia (SDEMI) was evaluated using human hepatocellular cells (HepG2), colorectal carcinoma cells (HT-29), and normal keratinocytes (HaCaT). Cells were treated with SDEMI for 4 and 24 h, then were assayed for levels of apoptosis, caspase-3, and Bcl-2 by flow cytometry, immunostaining, and Western blot, respectively. Significant differences between groups were determined using analysis of variance ( P < 0.05). For HepG2 and HT-29 cells treated with SDEMI, various cytotoxic effects were observed compared with control cells at all timepoints assayed ( P < 0.001). Furthermore, positive caspase-3 staining and down-regulation of Bcl-2 were observed, consistent with the induction of cell death detected in these cell lines. In contrast, treatment of HaCaT cells with SDEMI was associated with a protective effect compared with control cells at both timepoints ( P < 0.001). For example, increased expression of Bcl-2 and negative caspase-3 staining were detected. Taken together, these results suggest that SDEMI protects normal cells, while SDEMI mediates induction of apoptosis via down-regulation of Bcl-2 and involvement of caspase-3 in human carcinoma cells.

Publisher

SAGE Publications

Subject

General Biochemistry, Genetics and Molecular Biology

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