MiR-136 promotes apoptosis of glioma cells by targeting AEG-1 and Bcl-2

► MiR-136 is downregulated in human glioma cell lines and tissues. ► Ectopic expression of miR-136 is able to sensitize glioma cells to cisplatin-induced apoptosis. ► AEG-1 and BCL-2 are two directly targets of miR-136. ► Expression of ectopic AEG-1 or Bcl-2 partially abrogates the effect of miR-136...

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Veröffentlicht in:FEBS letters 2012-10, Vol.586 (20), p.3608-3612
Hauptverfasser: Yang, Yi, Wu, Jueheng, Guan, Hongyu, Cai, Junchao, Fang, Lishan, Li, Jun, Li, Mengfeng
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Sprache:eng
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Zusammenfassung:► MiR-136 is downregulated in human glioma cell lines and tissues. ► Ectopic expression of miR-136 is able to sensitize glioma cells to cisplatin-induced apoptosis. ► AEG-1 and BCL-2 are two directly targets of miR-136. ► Expression of ectopic AEG-1 or Bcl-2 partially abrogates the effect of miR-136. MicroRNAs have the capacity to coordinately repress multiple target genes and interfere with biological functions of the cell, such as proliferation and apoptosis. Here we report that miR-136 is downregulated in human glioma, and that the miRNA promotes apoptosis of glioma cells induced by chemotherapy. Two anti-apoptotic genes, AEG-1 and Bcl-2, are identified as targets of miR-136, and restoration of AEG-1 or Bcl-2 expression suppresses miR-136-enhanced apoptosis. Therefore, miR-136 might play a tumor-suppressive role in human glioma and thereby might represent a potential therapeutic strategy.
ISSN:0014-5793
1873-3468
DOI:10.1016/j.febslet.2012.08.003