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Saccharina japonica Extract Suppresses Stemness of Glioma Stem Cells by Degrading Epidermal Growth Factor Receptor/Epidermal Growth Factor Receptor Variant III.
Kim, So Yeon; Kim, Jeong-Yub; Shin, Woon-Seob; Lee, Seok Joon; Chi, Sung-Gil; Lee, Ji-Yun; Park, Myung-Jin.
Afiliação
  • Kim SY; 1 Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences , Research Center for Radio-Senescence, Seoul, Korea.
  • Kim JY; 2 School of Life Sciences and Biotechnology, Korea University , Seoul, Korea.
  • Shin WS; 1 Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences , Research Center for Radio-Senescence, Seoul, Korea.
  • Lee SJ; 3 Department of Pathology, College of Medicine, Korea University , Seoul, Korea.
  • Chi SG; 4 Department of Microbiology, Catholic Kwandong University College of Medicine , Gangneung, Korea.
  • Lee JY; 5 Department of Pharmacology, Catholic Kwandong University College of Medicine , Gangneung, Korea.
  • Park MJ; 2 School of Life Sciences and Biotechnology, Korea University , Seoul, Korea.
J Med Food ; 21(5): 496-505, 2018 May.
Article em En | MEDLINE | ID: mdl-29648968
ABSTRACT
Cancer stem cells, a small subpopulation of cells with stem cell-like characteristics found within most solid tumors, are widely reported to be responsible for the malignancy of aggressive cancer cells, and targeting these cells presents a sound therapeutic strategy for reducing the risk of tumor relapse. In the present study, we examined the effects of an extract of Saccharina japonica (ESJ) on glioblastoma stem cells (GSCs). Saccharina japonica is a member of the Phaeophyceae (brown algae) family, which displays biological activities, including antitumor effects. ESJ inhibited the sphere-forming ability of GSCs in vitro as evidenced by neurosphere formation and limiting dilution assays. Treatment with ESJ partially induced apoptosis, reduced cell invasiveness, and sensitized GSCs to ionizing radiation. In addition, ESJ inhibited the maintenance of stemness in GSCs by suppressing the expression of epidermal growth factor receptor (EGFR)/EGFR variant III (EGFRvIII) and Notch intracellular domain. Intriguingly, the observed ESJ-induced suppression also appeared to induce the proteasomal degradation of EGFR/EGFRvIII. Our results indicate that ESJ could be considered a potent therapeutic adjuvant that targets GSCs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Phaeophyceae / Receptores ErbB Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Phaeophyceae / Receptores ErbB Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article