Tumour-suppressive microRNA-24-1 inhibits cancer cell proliferation through targeting FOXM1 in bladder cancer

被引:78
|
作者
Inoguchi, Satoru [1 ]
Seki, Naohiko [2 ]
Chiyomaru, Takeshi [1 ]
Ishihara, Tomoaki [1 ]
Matsushita, Ryosuke [1 ]
Mataki, Hiroko [3 ]
Itesako, Toshihiko [1 ]
Tatarano, Shuichi [1 ]
Yoshino, Hirofumi [1 ]
Goto, Yusuke [2 ]
Nishikawa, Rika [2 ]
Nakagawa, Masayuki [1 ]
Enokida, Hideki [1 ]
机构
[1] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Urol, Kagoshima 8908520, Japan
[2] Chiba Univ, Grad Sch Med, Dept Funct Genom, Chiba, Japan
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Pulm Med, Kagoshima 8908520, Japan
关键词
microRNA; microRNA-24-1; Forkhead box protein M1; Bladder cancer; Tumour suppressor; FUNCTIONAL-SIGNIFICANCE; CARCINOMA; INVASION; PROGRESSION; METASTASIS; EXPRESSION; IDENTIFICATION; MECHANISMS; MIGRATION; MIR-133A;
D O I
10.1016/j.febslet.2014.06.058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:3170 / 3179
页数:10
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