| Literature DB >> 19135980 |
Hongping Xia1, Yanting Qi, Samuel S Ng, Xiaona Chen, Shen Chen, Marong Fang, Dan Li, Yu Zhao, Ruiguang Ge, Guo Li, Yangchao Chen, Ming-Liang He, Hsiang-fu Kung, Lihui Lai, Marie C Lin.
Abstract
MicroRNAs (miRNAs) are non-protein-coding 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 downstream 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 in glioma cells by targeting cell cycle-related molecules.Entities:
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Year: 2009 PMID: 19135980 DOI: 10.1016/j.bbrc.2008.12.169
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575