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Circadian gene Clock contributes to cell proliferation and migration of glioma and is directly regulated by tumor-suppressive miR-124

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机构: [1]Chinese Acad Med Sci, State Key Lab Med Mol Biol, Dept Mol Biol & Biochem, Inst Basic Med Sci, Beijing 100005, Peoples R China; [2]Peking Union Med Coll, Beijing 100005, Peoples R China; [3]Beijing Tiantan Hosp, Dept Neurosurg, Beijing 100050, Peoples R China
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关键词: Glioma CLOCK miR-124 NF-kappa B

摘要:
Although the roles of circadian Clock genes and microRNAs in tumorigenesis have been profoundly studied, mechanisms of cross-talk between them in regulation of gliomagenesis are poorly understood. Here we show that the expression level of CLOCK is significantly increased in high-grade human glioma tissues and glioblastoma cell lines. In contrast miR-124 is attenuated in similar samples. Further studies show that Clock is a direct target of miR-124, and either restoration of miR-124 or silencing of CLOCK can reduce the activation of NF-kappa B. In conclusion, we suggest that as a target of glioma suppressor miR-124, CLOCK positively regulates glioma proliferation and migration by reinforcing NF-kappa B activity. (C) 2013 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.

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出版当年[2012]版:
大类 | 3 区 生物
小类 | 3 区 生化与分子生物学 3 区 生物物理 4 区 细胞生物学
最新[2023]版:
大类 | 4 区 生物学
小类 | 4 区 生化与分子生物学 4 区 生物物理 4 区 细胞生物学
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出版当年[2011]版:
Q2 CELL BIOLOGY Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Q2 BIOPHYSICS
最新[2023]版:
Q2 BIOPHYSICS Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Q3 CELL BIOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2011版] 出版当年五年平均 出版前一年[2010版] 出版后一年[2012版]

第一作者:
第一作者机构: [1]Chinese Acad Med Sci, State Key Lab Med Mol Biol, Dept Mol Biol & Biochem, Inst Basic Med Sci, Beijing 100005, Peoples R China; [2]Peking Union Med Coll, Beijing 100005, Peoples R China;
通讯作者:
通讯机构: [1]Chinese Acad Med Sci, State Key Lab Med Mol Biol, Dept Mol Biol & Biochem, Inst Basic Med Sci, Beijing 100005, Peoples R China; [2]Peking Union Med Coll, Beijing 100005, Peoples R China;
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