MicroRNA-15b regulates cell cycle progression by targeting cyclins in glioma cells

被引:137
作者
Xia, Hongping [2 ]
Qi, Yanting [1 ]
Ng, Samuel S. [2 ]
Chen, Xiaona [1 ]
Chen, Shen [3 ]
Fang, Marong [2 ,4 ]
Li, Dan [1 ]
Zhao, Yu [1 ]
Ge, Ruiguang [3 ]
Li, Guo [3 ]
Chen, Yangchao [5 ]
He, Ming-Liang [5 ]
Kung, Hsiang-fu [1 ,3 ,5 ]
Lai, Lihui [1 ]
Lin, Marie C. [1 ,2 ]
机构
[1] E China Normal Univ, Inst Mol & Chem Biol, Shanghai 200062, Peoples R China
[2] Univ Hong Kong, Dept Chem, Inst Mol Technol, Integrat Chem Biol Lab, Hong Kong, Hong Kong, Peoples R China
[3] Sun Yat Sen Univ, Coll Life Sci, Lab Integrat Biol, Guangzhou 510275, Guangdong, Peoples R China
[4] Zhejiang Univ, Sch Med, Inst Cell Biol, Hangzhou 310058, Zhejiang, Peoples R China
[5] Chinese Univ Hong Kong, State Key Lab Oncol S China, Stanley Ho Ctr Emerging Infect Dis, Shatin, Hong Kong, Peoples R China
基金
美国国家科学基金会;
关键词
MicroRNA; MiR-15b; Cell cycle; CCNE1; Glioblastoma; CENTRAL-NERVOUS-SYSTEM; TUMORS; P27(KIP1); PROGNOSIS;
D O I
10.1016/j.bbrc.2008.12.169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are non-protein-cocling RNAs that function as post-transcriptional gene regulators. Recent evidence has shown that miRNA plays a pivotal role in the development of many cancers including glioma, a lethal brain cancer. We have recently compared the miRNA expression profiles between normal brain and glioma tissues from Chinese patients by miRNA microarray and identified a panel of differentially expressed miRNAs. Here, we studied the function of one miRNA, miR-15b, in glioma carcinogenesis and elucidated its down stream targets. Over-expression of miR-15b resulted in cell cycle arrest at G0/G1 phase while suppression of miR-15b expression resulted in a decrease of cell populations in G0/G1 and a corresponding increase of cell populations in S phase. We further showed that CCNE1 (encoding cyclin E1) is one of the downstream targets of miR-15b. Taken together, our findings indicate that miR-15b regulates cell cycle progression ill glioma cells by targeting cell cycle-related molecules. (c) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:205 / 210
页数:6
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