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Antitumor activity of Brazilian red propolis fractions against Hep-2 cancer cell line.
Frozza, Caroline Olivieri da Silva; Santos, Denis Amilton; Rufatto, Luciane Corbellini; Minetto, Luciane; Scariot, Fernando Joel; Echeverrigaray, Sergio; Pich, Claus Tröger; Moura, Sidnei; Padilha, Francine Ferreira; Borsuk, Sibele; Savegnago, Lucielli; Collares, Tiago; Seixas, Fabiana Kömmling; Dellagostin, Odir; Roesch-Ely, Mariana; Henriques, João Antonio Pêgas.
Afiliação
  • Frozza CODS; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Santos DA; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Rufatto LC; Laboratory of Natural and Synthetic Products, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Minetto L; Laboratory of Natural and Synthetic Products, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Scariot FJ; Laboratory of Applied Microbiology, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Echeverrigaray S; Laboratory of Applied Microbiology, Biotechnology Institute, University of Caxias do Sul, RS, Brazil; Cytogene Molecular Diagnostics Company, RS, Brazil.
  • Pich CT; NITBIO Federal University of Santa Catarina, Araranguá, SC, Brazil.
  • Moura S; Laboratory of Natural and Synthetic Products, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Padilha FF; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • Borsuk S; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • Savegnago L; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • Collares T; Cancer Biotechnology Laboratory, Research Group on Cellular and Molecular Oncology, Postgraduate Program in Biotechnology, Technology Development Center, Federal University of Pelotas, Pelotas, RS, Brazil.
  • Seixas FK; Cancer Biotechnology Laboratory, Research Group on Cellular and Molecular Oncology, Postgraduate Program in Biotechnology, Technology Development Center, Federal University of Pelotas, Pelotas, RS, Brazil.
  • Dellagostin O; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • Roesch-Ely M; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Henriques JAP; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil. Electronic address: pegas.henriques@gmail.com.
Biomed Pharmacother ; 91: 951-963, 2017 Jul.
Article em En | MEDLINE | ID: mdl-28514834
Continuous increases in the rates of tumor diseases have highlighted the need for identification of novel and inexpensive antitumor agents from natural sources. In this study, we investigated the effects of enriched fraction from hydroalcoholic Brazilian red propolis extract against Hep-2 cancer cell line. Initially 201 fractions were arranged in 12 groups according to their chromatographic characteristics (A-L). After an in vitro cell viability screening, J and L were further selected as promising enriched fractions for this study. The chemical characterization was performed and Biochanin A, Formononetin, and Liquiritigenin compounds were quantified. Through MTT viability assay and morphological changes observed by Giemsa and DAPI staining, the results showed that red propolis inhibited cancer cells growth. Flow cytometry results indicated effects that were partly mediated through programmed cell death as confirmed by externalization of phosphatidylserine, DNA cleaved assay, increase at SUB G1-G0 phase in cell cycle analysis and loss of mitochondrial membrane potential. In conclusion, our results demonstrated that red propolis enriched fractions promoted apoptotic effects in human cancer cells through the mechanisms involving mitochondrial perturbation. Therefore, red propolis fractions contain candidate agents for adjuvant cancer treatment, which further studies should elucidate the comprehensive mechanistic pathways.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Própole / Neoplasias / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Própole / Neoplasias / Antineoplásicos Tipo de estudo: Prognostic_studies Limite: Humans País como assunto: America do sul / Brasil Idioma: En Ano de publicação: 2017 Tipo de documento: Article