中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Oligosaccharide G19 inhibits U-87 MG human glioma cells growth in vitro and in vivo by targeting epidermal growth factor (EGF) and activating p53/p21 signaling

文献类型:期刊论文

作者Liu, Hailing2,3; Zhou, Ling2,3; Shi, Songshan1; Wang, Ying3; Ni, Xinyan3; Xiao, Fei3; Wang, Shunchun1; Li, Ping2; Ding, Kan3
刊名GLYCOBIOLOGY
出版日期2014-08
卷号24期号:8
ISSN号0959-6658
关键词apoptosis cell cycle arrest glioma oligosaccharide G19 p53
文献子类Article
英文摘要G19 is a novel homogeneous sulfated oligosaccharide, prepared from Grateloupia filicina (G. filicina). In the present study, we firstly reported that oligosaccharide G19 exhibited a dose-and time-dependent anti-proliferation effect against U-87 MG human glioma cells. Further studies indicated that G19 strongly bound to epidermal growth factor (EGF), suppressed epidermal growth factor receptor (EGFR) phosphorylation and interrupted the phosphatidylinositol-3 kinase (PI3K)/Akt pathway in the cancer cells. Moreover, G19 elevated intracellular reactive oxygen species (ROS) levels and caused endogenous DNA damage. These actions were associated with activation of ataxia telangiectasia-mutated (ATM)/checkpoint kinase 2 (Chk2) pathway. The down-regulation of MDM2 with stabilizing p53 and the nuclear location of p21 were induced by G19 to cause cell cycle arrest and apoptosis to some extent. Meanwhile, intrinsic mitochondrial pathway and extrinsic death receptor pathway were involved in G19-mediated apoptosis. Pre-treatment with free radical scavenger N-acetyl-L-cysteine (NAC) nearly completely inversed G19-induced cell growth inhibition, cell cycle arrest and apoptosis in U-87 MG cells. Importantly, G19 could inhibit the growth of U-87 MG tumor cells xenograft in nude mice. The results suggested that G19 could be served as a new targeting drug candidate for human glioma treatment.
WOS关键词NF-KAPPA-B ; DOUBLE-STRAND BREAKS ; CANCER-CELLS ; DNA-DAMAGE ; IONIZING-RADIATION ; TRANSCRIPTIONAL ACTIVATION ; CARCINOMA-CELLS ; FACTOR RECEPTOR ; CYCLE ARREST ; COMET ASSAY
资助项目New Drug Creation and Manufacturing Program[2012ZX09301001-003] ; National Science Fund for Distinguished Young Scholars in China[81125025] ; National Natural Science Foundation of China (NSFC)[31230022] ; National Natural Science Foundation of China (NSFC)[81171914]
WOS研究方向Biochemistry & Molecular Biology
语种英语
出版者OXFORD UNIV PRESS INC
WOS记录号WOS:000339418000008
源URL[http://119.78.100.183/handle/2S10ELR8/276972]  
专题药理学第三研究室
通讯作者Ding, Kan
作者单位1.Shanghai Univ Tradit Chinese Med, Inst Chinese Mat Med, Key Lab Standardizat Chinese Med, Minist Educ, Shanghai 201203, Peoples R China
2.China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Peoples R China;
3.Chinese Acad Sci, Glycobiol & Glycochem Lab, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China;
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GB/T 7714
Liu, Hailing,Zhou, Ling,Shi, Songshan,et al. Oligosaccharide G19 inhibits U-87 MG human glioma cells growth in vitro and in vivo by targeting epidermal growth factor (EGF) and activating p53/p21 signaling[J]. GLYCOBIOLOGY,2014,24(8).
APA Liu, Hailing.,Zhou, Ling.,Shi, Songshan.,Wang, Ying.,Ni, Xinyan.,...&Ding, Kan.(2014).Oligosaccharide G19 inhibits U-87 MG human glioma cells growth in vitro and in vivo by targeting epidermal growth factor (EGF) and activating p53/p21 signaling.GLYCOBIOLOGY,24(8).
MLA Liu, Hailing,et al."Oligosaccharide G19 inhibits U-87 MG human glioma cells growth in vitro and in vivo by targeting epidermal growth factor (EGF) and activating p53/p21 signaling".GLYCOBIOLOGY 24.8(2014).

入库方式: OAI收割

来源:上海药物研究所

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