RETRACTED: MicroRNA-140 represses glioma growth and metastasis by directly targeting ADAM9 (Retracted Article)

被引:30
作者
Liu, Xiaogang [1 ,2 ]
Wang, Shanjun [1 ]
Yuan, Aiqin [1 ]
Yuan, Xunhui [1 ]
Liu, Bing [2 ]
机构
[1] Yidu Cent Hosp Weifang, Dept Neurosurg, Weifang 262500, Shandong, Peoples R China
[2] Weifang Med Univ, Affiliated Hosp, Dept Neurosurg, 2428 Yuhe Rd, Weifang 261030, Shandong, Peoples R China
关键词
microRNA-140; glioma; proliferation; migration; invasion; a disintegrin and metalloproteinase 9; HEPATOCELLULAR-CARCINOMA; TUMOR-SUPPRESSOR; POOR-PROGNOSIS; CELL INVASION; CANCER-CELLS; STEM-CELLS; EXPRESSION; PROLIFERATION; MIGRATION; PROGRESSION;
D O I
10.3892/or.2016.5007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioma is the most frequent primary malignant tumor of the human brain. Recently, great progress has been made in the combined therapy of glioma. However, the clinical effects of these treatments and prognosis for patients with glioma remains poor. MicroRNAs (miRNAs) have been demonstrated to play important roles in the initiation and progression of various types of human cancers, also including glioma. The present study investigated the expression patterns of microRNA-140 (miR-140) in glioma, and the roles of miR-140 in glioma cell proliferation, migration and invasion. The results showed that miR-140 was significantly downreuglated in glioma tissues and cell lines, and low expression levels of miR-140 were correlated with World Health Organization (WHO) grade and Karnofsky performance score (KPS) of glioma patients. Restoration of miR-140 obviously suppressed glioma cell proliferation, migration and invasion. In addition, a disintegrin and metalloproteinase 9 (ADAM9) was identified as a novel direct target gene of miR-140 in glioma. Furthermore, knockdown of ADAM9 simulated the tumor suppressor functions of miR-140, while overexpression of ADAM9 abrogated these suppressive effects induced by miR-140 in glioma cells. In conclusion, the present study demonstrated the expression and clinical roles of miR-140 in glioma and suggested that miR-140 inhibited proliferation, migration and invasion of glioma cells, partially at least via suppressing ADAM9 expression. Therefore, miR-140 may be a novel candidate target for the development of therapeutic strategies for patients with glioma.
引用
收藏
页码:2329 / 2338
页数:10
相关论文
共 49 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]  
[Anonymous], 2007, ACTA NEUROPATHOL, DOI DOI 10.1007/s00401-007-0243-4
[3]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[4]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[5]   Adams: Key components in EGFR signalling and development [J].
Blobel, CP .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (01) :32-43
[6]   Fisetin suppresses ADAM9 expression and inhibits invasion of glioma cancer cells through increased phosphorylation of ERK1/2 [J].
Chen, Chien-Min ;
Hsieh, Yi-Hsien ;
Hwang, Jin-Ming ;
Jan, Hsun-Jin ;
Hsieh, Shu-Ching ;
Lin, Shin-Huey ;
Lai, Chung-Yu .
TUMOR BIOLOGY, 2015, 36 (05) :3407-3415
[7]   VHL regulates the effects of miR-23b on glioma survival and invasion via suppression of HIF-1α/VEGF and β-catenin/Tcf-4 signaling [J].
Chen, Lingchao ;
Han, Lei ;
Zhang, Kailiang ;
Shi, Zhendong ;
Zhang, Junxia ;
Zhang, Anling ;
Wang, Yongzhi ;
Song, Yijun ;
Li, Yongli ;
Jiang, Tao ;
Pu, Peiyu ;
Jiang, Chuanlu ;
Kang, Chunsheng .
NEURO-ONCOLOGY, 2012, 14 (08) :1026-1036
[8]   Association between glioma susceptibility loci and tumour pathology defines specific molecular etiologies [J].
Di Stefano, Anna Luisa ;
Enciso-Mora, Victor ;
Marie, Yannick ;
Desestret, Virginie ;
Labussire, Marianne ;
Boisselier, Blandine ;
Mokhtari, Karima ;
Idbaih, Ahmed ;
Hoang-Xuan, Khe ;
Delattre, Jean-Yves ;
Houlston, Richard S. ;
Sanson, Marc .
NEURO-ONCOLOGY, 2013, 15 (05) :542-547
[9]   MiR-140-3p suppressed cell growth and invasion by downregulating the expression of ATP8A1 in non-small cell lung cancer [J].
Dong, Wei ;
Yao, Chunping ;
Teng, Xuepeng ;
Chai, Jie ;
Yang, Xinhua ;
Li, Baosheng .
TUMOR BIOLOGY, 2016, 37 (03) :2973-2985
[10]   Role of ADAMS in Cancer Formation and Progression [J].
Duffy, Michael J. ;
McKiernan, Eaclaoin ;
O'Donovan, Norma ;
McGowan, Patricia M. .
CLINICAL CANCER RESEARCH, 2009, 15 (04) :1140-1144