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Protective Effect of an Isoflavone, Tectorigenin, Against Oxidative Stress-induced Cell Death via Catalase Activation.
Zhang, Rui; Piao, Mei Jing; Oh, Min Chang; Park, Jeong Eon; Shilnikova, Kristina; Moon, Yu Jin; Kim, Dong Hyun; Jung, Uhee; Kim, In Gyu; Hyun, Jin Won.
Afiliação
  • Zhang R; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea; School of Medical Science and Laboratory Medicine, Jiangsu University, Jiangsu, China.
  • Piao MJ; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Oh MC; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Park JE; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Shilnikova K; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Moon YJ; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Kim DH; Department of Microbial Chemistry, College of Pharmacy, Kyung Hee University, Seoul, Korea.
  • Jung U; Radiation Biotechnology Research Division, Korea Atomic Energy Research Institute, Jeongeup, Korea.
  • Kim IG; Department of Radiation Biology, Environmental Radiation Research Group, Korea Atomic Energy Research Institute, Daejeon, Korea; Department of Radiation Biotechnology and Applied Radioisotope, Korea University of Science and Technology, Daejeon, Korea.
  • Hyun JW; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
J Cancer Prev ; 21(4): 257-263, 2016 Dec.
Article em En | MEDLINE | ID: mdl-28053960
BACKGROUND: Isoflavones are biologically active compounds that occur naturally in a variety of plants, with relatively high levels in soybean. Tectorigenin, an isoflavone, protects against hydrogen peroxide (H2O2)-induced cell damage. However, the underlying mechanism is unknown. METHODS: The MTT assay was performed to determine cell viability. Catalase activity was assessed by determining the amount of enzyme required to degrade 1 µM H2O2. Protein expression of catalase, phospho-extracellular signal-regulated kinase (ERK), IκB-α, and NF-κB were evaluated by Western blot analysis. A mobility shift assay was performed to assess the DNA-binding ability of NF-κB. Transient transfection and a NF-κB luciferase assay were performed to assess transcriptional activity. RESULTS: Tectorigenin reduced H2O2-induced death of Chinese hamster lung fibroblasts (V79-4). In addition, tectorigenin increased the activity and protein expression of catalase. Blockade of catalase activity attenuated the protective effect of tectorigenin against oxidative stress. Furthermore, tectorigenin enhanced phosphorylation of ERK and nuclear expression of NF-κB, while inhibition of ERK and NF-κB attenuated the protective effect of tectorigenin against oxidative stress. CONCLUSIONS: Tectorigenin protects cells against oxidative damage by activating catalase and modulating the ERK and NF-κB signaling pathway.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2016 Tipo de documento: Article