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Hsa-miR-125b suppresses bladder cancer development by down-regulating oncogene SIRT7 and oncogenic long non-coding RNA MALAT1

•Hsa-miR-125b and SIRT7/MALAT1 are inversely expressed in bladder cancer.•Hsa-miR-125b inhibits bladder cancer cell growth and motility, and increases apoptosis.•Hsa-miR-125b downregulates oncogene SIRT7 in bladder cancer.•Hsa-miR-125b downregulates oncogenic long non-coding RNA MALAT1 in bladder ca...

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Published in:FEBS letters 2013-11, Vol.587 (23), p.3875-3882
Main Authors: Han, Yonghua, Liu, Yuchen, Zhang, Hu, Wang, Tiantian, Diao, Ruiying, Jiang, Zhimao, Gui, Yaoting, Cai, Zhiming
Format: Article
Language:English
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Summary:•Hsa-miR-125b and SIRT7/MALAT1 are inversely expressed in bladder cancer.•Hsa-miR-125b inhibits bladder cancer cell growth and motility, and increases apoptosis.•Hsa-miR-125b downregulates oncogene SIRT7 in bladder cancer.•Hsa-miR-125b downregulates oncogenic long non-coding RNA MALAT1 in bladder cancer.•Hsa-miR-125b suppresses bladder cancer development via inhibiting SIRT7 and MALAT1. MicroRNAs mainly inhibit coding genes and long non-coding RNA expression. Here, we report that hsa-miR-125b and oncogene SIRT7/oncogenic long non-coding RNA MALAT1 were inversely expressed in bladder cancer. Hsa-miR-125b mimic down-regulated, whereas hsa-miR-125b inhibitor up-regulated the expression of SIRT7 and MALAT1. Binding sites were confirmed between hsa-miR-125b and SIRT7/MALAT1. Up-regulation of hsa-miR-125b or down-regulation of SIRT7 inhibited proliferation, motility and increased apoptosis. The effects of up-regulation of hsa-miR-125b were similar to that of silencing MALAT1 in bladder cancer as we had previously described. These data suggest that hsa-miR-125b suppresses bladder cancer development via inhibiting SIRT7 and MALAT1.
ISSN:0014-5793
1873-3468
DOI:10.1016/j.febslet.2013.10.023