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

  • Hongping Xia
  • , 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

Research output: Contribution to journalArticlepeer-review

135 Scopus citations

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.

Original languageEnglish
Pages (from-to)205-210
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume380
Issue number2
DOIs
StatePublished - 6 Mar 2009

Keywords

  • CCNE1
  • Cell cycle
  • Glioblastoma
  • MicroRNA
  • MiR-15b

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