MicroRNA-635 inhibits the malignancy of osteosarcoma by inducing apoptosis

被引:12
作者
Tian, Linqiang [1 ]
Guo, Zhihao [1 ]
Wang, Hongwei [1 ]
Liu, Xiaotan [1 ]
机构
[1] Xinxiang Med Univ, Affiliated Hosp 3, Dept Orthoped Surg, East Hualan Ave, Xinxiang 453003, Henan, Peoples R China
关键词
microRNA-635; osteosarcoma; proliferation; migration; apoptosis; CELL LUNG-CANCER; TUMOR-SUPPRESSOR; CARCINOMA-CELLS; EXPRESSION; MIGRATION; INVASION; METASTASIS; INCREASES;
D O I
10.3892/mmr.2017.7127
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent evidence has suggested that microRNAs (miRs), which are a class of non-coding RNAs, serve diverse roles in tumorigenesis. However, the role of miR-635 in osteosarcoma (OS) remains unknown. The present study revealed that miR-635 may be a tumor suppressive miR. The expression of miR-635 was significantly decreased in OS specimens. In addition, the proliferation and invasion of OS cells transfected with miR-635 may be effectively attenuated. Transfection of cells with miR-635 may further inhibit tumor growth in vivo. miR-635 may antagonize tumorigenesis of OS possibly by inducing apoptosis, as demonstrated by flow cytometric analysis and caspase-3 kinase assays. The data of the present study suggested that miR-635 may be a novel tumor suppressor and may serve as a putative diagnostic marker for patients with OS.
引用
收藏
页码:4829 / 4834
页数:6
相关论文
共 22 条
[1]   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
[2]   Non-small-cell lung cancer and miRNAs: novel biomarkers and promising tools for treatment [J].
Feng, Bing ;
Zhang, Kai ;
Wang, Rui ;
Chen, Longbang .
CLINICAL SCIENCE, 2015, 128 (10) :619-634
[3]   Functional elucidation of MiR-34 in osteosarcoma cells and primary tumor samples [J].
He, Chunlei ;
Xiong, Jianyi ;
Xu, Xiaoping ;
Lu, Wei ;
Liu, Lijun ;
Xiao, Deming ;
Wang, Daping .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2009, 388 (01) :35-40
[4]   Bone tumors: osteosarcoma and Ewing's sarcoma [J].
Heare, Travis ;
Hensley, Mary A. ;
Dell'Orfano, Shelley .
CURRENT OPINION IN PEDIATRICS, 2009, 21 (03) :365-372
[5]   miR-20a Encoded by the miR-17-92 Cluster Increases the Metastatic Potential of Osteosarcoma Cells by Regulating Fas Expression [J].
Huang, Gangxiong ;
Nishimoto, Kazumasa ;
Zhou, Zhichao ;
Hughes, Dennis ;
Kleinerman, Eugenie S. .
CANCER RESEARCH, 2012, 72 (04) :908-916
[6]   MicroRNA-138 functions as a tumor suppressor in osteosarcoma by targeting differentiated embryonic chondrocyte gene 2 [J].
Jiang, Baoen ;
Mu, Weidong ;
Wang, Jiangquan ;
Lu, Jianshu ;
Jiang, Shanyong ;
Li, Liang ;
Xu, Haining ;
Tian, Hongyan .
JOURNAL OF EXPERIMENTAL & CLINICAL CANCER RESEARCH, 2016, 35
[7]  
Jin H, 2015, INT J CLIN EXP PATHO, V8, P8075
[8]   Genome-wide microRNA profiling of human temporal lobe epilepsy identifies modulators of the immune response [J].
Kan, Anne A. ;
van Erp, Susan ;
Derijck, Alwin A. H. A. ;
de Wit, Marina ;
Hessel, Ellen V. S. ;
O'Duibhir, Eoghan ;
de Jager, Wilco ;
Van Rijen, Peter C. ;
Gosselaar, Peter H. ;
de Graan, Pierre N. E. ;
Pasterkamp, R. Jeroen .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2012, 69 (18) :3127-3145
[9]   miRBase: annotating high confidence microRNAs using deep sequencing data [J].
Kozomara, Ana ;
Griffiths-Jones, Sam .
NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) :D68-D73
[10]   The functions of microRNAs in pluripotency and reprogramming [J].
Leonardo, Trevor R. ;
Schultheisz, Heather L. ;
Loring, Jeanne F. ;
Laurent, Louise C. .
NATURE CELL BIOLOGY, 2012, 14 (11) :1114-1121