| Literature DB >> 24999187 |
Satoru Inoguchi1, Naohiko Seki2, Takeshi Chiyomaru1, Tomoaki Ishihara1, Ryosuke Matsushita1, Hiroko Mataki3, Toshihiko Itesako1, Shuichi Tatarano1, Hirofumi Yoshino1, Yusuke Goto2, Rika Nishikawa2, Masayuki Nakagawa1, Hideki Enokida4.
Abstract
Here, we found that microRNA-24-1 (miR-24-1) is significantly reduced in bladder cancer (BC) tissues, suggesting that it functions as a tumour suppressor. Restoration of mature miR-24-1 inhibits cancer cell proliferation and induces apoptosis. Forkhead box protein M1 (FOXM1) is a direct target gene of miR-24-1, as shown by genome-wide gene expression analysis and luciferase reporter assay. Overexpressed FOXM1 is confirmed in BC clinical specimens, and silencing of FOXM1 induces apoptosis in cancer cell lines. Our data demonstrate that the miR-24-1-FOXM1 axis contributes to cancer cell proliferation in BC, and elucidation of downstream signalling will provide new insights into the molecular mechanisms of BC oncogenesis.Entities:
Keywords: Bladder cancer; Forkhead box protein M1; Tumour suppressor; microRNA; microRNA-24-1
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Year: 2014 PMID: 24999187 DOI: 10.1016/j.febslet.2014.06.058
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124