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Menadione and protocatechuic acid: A drug combination with antitumor effects in murine osteosarcoma cells.
Inacio, Kelly Karina; Pessoa, Adriano de Souza; Tokuhara, Cintia Kazuko; Pagnan, Ana Lígia; Sanches, Mariana Liessa Rovis; Fakhoury, Vanessa Svizzero; Oliveira, Gabriela Silva Neubern de; Oliveira, Flavia Amadeu de; Ximenes, Valdecir Farias; Oliveira, Rodrigo Cardoso de.
Affiliation
  • Inacio KK; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.
  • Pessoa AS; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.
  • Tokuhara CK; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.
  • Pagnan AL; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.
  • Sanches MLR; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.
  • Fakhoury VS; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.
  • Oliveira GSN; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil.
  • Oliveira FA; Sanford Children's Health Research Center. Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
  • Ximenes VF; Department of Chemistry, Faculty of Sciences, UNESP, São Paulo State University, Bauru, São Paulo, Brazil.
  • Oliveira RC; Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Brazil. Electronic address: rodrigocardoso@usp.br.
Arch Biochem Biophys ; 751: 109840, 2024 01.
Article in En | MEDLINE | ID: mdl-38040223
Osteosarcoma (OS) is a primary malignant bone tumor that has an abnormal expression of oncogenesis and tumor suppressors and causes dysregulation of various signaling pathways. Thus, novel therapeutic strategies for OS are needed to overcome the resistance of traditional treatments. This study evaluated the cytotoxic and anticancer effects of the association between menadione (MEN) and protocatechuic acid (PCA) in murine OS cells (UMR-106). The concentrations were 3.12 µM of isolated MEN, 500 µM of isolated PCA, and their associations. We performed cell viability assays, morphology modification analysis, cell migration by the wound-healing method, apoptosis by flow cytometry, reactive oxygen species (ROS) production, gene expression of NOX by RT-qPCR, and degradation of MMP-2 and 9 by zymography. Our results showed that the association of MEN+PCA was more effective in OS cells than the compounds alone. The association decreased cell viability, delayed cell migration, and decreased the expression of NOX-2 and ROS. In addition, the MEN+PCA association induced a slight increase in the apoptotic process. In summary, the association can enhance the compound's antitumor effects and establish a higher selectivity for tumor cells, possibly caused by significant mitochondrial damage and antioxidant properties.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteosarcoma Limits: Animals / Humans Language: En Journal: Arch Biochem Biophys Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteosarcoma Limits: Animals / Humans Language: En Journal: Arch Biochem Biophys Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United States