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海带提取物通过降解表皮生长因子受体/表皮生长因子受体III型变体抑制胶质瘤干细胞的干性。

Saccharina japonica Extract Suppresses Stemness of Glioma Stem Cells by Degrading Epidermal Growth Factor Receptor/Epidermal Growth Factor Receptor Variant III.

作者信息

Kim So Yeon, Kim Jeong-Yub, Shin Woon-Seob, Lee Seok Joon, Chi Sung-Gil, Lee Ji-Yun, Park Myung-Jin

机构信息

1 Division of Radiation Cancer Research, Korea Institute of Radiological and Medical Sciences , Research Center for Radio-Senescence, Seoul, Korea.

2 School of Life Sciences and Biotechnology, Korea University , Seoul, Korea.

出版信息

J Med Food. 2018 May;21(5):496-505. doi: 10.1089/jmf.2017.3992. Epub 2018 Mar 14.

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.

摘要

癌症干细胞是在大多数实体瘤中发现的具有干细胞样特征的一小部分细胞,广泛报道其与侵袭性癌细胞的恶性肿瘤有关,靶向这些细胞为降低肿瘤复发风险提供了一种合理的治疗策略。在本研究中,我们研究了海带提取物(ESJ)对胶质母细胞瘤干细胞(GSCs)的影响。海带是褐藻门的成员,具有包括抗肿瘤作用在内的生物活性。ESJ在体外抑制了GSCs的成球能力,这通过神经球形成和有限稀释分析得到证明。ESJ处理部分诱导了细胞凋亡,降低了细胞侵袭性,并使GSCs对电离辐射敏感。此外,ESJ通过抑制表皮生长因子受体(EGFR)/EGFR变异体III(EGFRvIII)和Notch细胞内结构域的表达来抑制GSCs干性的维持。有趣的是,观察到的ESJ诱导的抑制似乎还诱导了EGFR/EGFRvIII的蛋白酶体降解。我们的结果表明,ESJ可被视为一种靶向GSCs的有效治疗佐剂。

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