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Proteomic analysis identifies differentially expressed proteins after red propolis treatment in Hep-2 cells.
Frozza, Caroline Olivieri da Silva; Ribeiro, Tanara da Silva; Gambato, Gabriela; Menti, Caroline; Moura, Sidnei; Pinto, Paulo Marcos; Staats, Charley Christian; Padilha, Francine Ferreira; Begnini, Karine Rech; de Leon, Priscila Marques Moura; Borsuk, Sibele; Savegnago, Lucielli; Dellagostin, Odir; Collares, Tiago; Seixas, Fabiana Kömmling; Henriques, João Antonio Pêgas; Roesch-Ely, Mariana.
Afiliação
  • Frozza CO; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Ribeiro Tda S; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Gambato G; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Menti C; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Moura S; Laboratory of Biotechnology of Natural and Synthetics Products, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Pinto PM; Laboratory of Applied Proteomics Campus São Gabriel, Federal University of Pampa, São Gabriel, RS, Brazil.
  • Staats CC; Biotechnology Center, Federal University of Rio Grande do Sul, Av. Bento Gonçalves, Porto Alegre, RS, Brazil.
  • Padilha FF; Program on Health and Environment, Tiradentes University, Aracaju, SE, Brazil.
  • Begnini KR; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • de Leon PM; 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.
  • Dellagostin O; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • Collares T; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • Seixas FK; Biotechnology Unit, Center for Technology Development, Federal University of Pelotas, RS, Brazil.
  • Henriques JA; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil.
  • Roesch-Ely M; Laboratory of Genomics, Proteomics and DNA Repair, Biotechnology Institute, University of Caxias do Sul, RS, Brazil. Electronic address: mrely@ucs.br.
Food Chem Toxicol ; 63: 195-204, 2014 Jan.
Article em En | MEDLINE | ID: mdl-24239894
ABSTRACT
Here we investigated alterations in the protein profile of Hep-2 treated with red propolis using two-dimensional electrophoresis associated to mass spectrometry and apoptotic rates of cells treated with and without red propolis extracts through TUNEL and Annexin-V assays. A total of 325 spots were manually excised from the two-dimensional gel electrophoresis and 177 proteins were identified using LC-MS-MS. Among all proteins identified that presented differential expression, most were down-regulated in presence of red propolis extract at a concentration of 120 µg/mL (IC50) GRP78, PRDX2, LDHB, VIM and TUBA1A. Only two up-regulated proteins were identified in this study in the non-cytotoxic (6 µg/mL) red propolis treated group RPLP0 and RAD23B. TUNEL staining assay showed a markedly increase in the mid- to late-stage apoptosis of Hep-2 cells induced by red propolis at concentrations of 60 and 120 µg/mL when compared with non-treated cells. The increase of late apoptosis was confirmed by in situ Annexin-V analysis in which red propolis extract induced late apoptosis in a dose-dependent manner. The differences in tumor cell protein profiles warrant further investigations including isolation of major bioactive compounds of red propolis in different cell lines using proteomics and molecular tests to validate the protein expression here observed.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Própole / Proteínas de Neoplasias Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Própole / Proteínas de Neoplasias Limite: Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article