MicroRNA-101 inhibits the metastasis of osteosarcoma cells by downregulation of EZH2 expression

被引:64
作者
Zhang, Kailiang [1 ]
Zhang, Yinglong [1 ]
Ren, Kun [1 ]
Zhao, Guangyi [1 ]
Yan, Kang [1 ]
Ma, Baoan [1 ]
机构
[1] Fourth Mil Med Univ, Tangdu Hosp, Dept Orthoped, Xian 710038, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
microRNA-101; osteosarcoma; enhancer of zeste homolog 2; metastasis; migration; invasion; ZESTE HOMOLOG 2; GROUP PROTEIN EZH2; PROSTATE-CANCER; GASTRIC-CANCER; BREAST-CANCER; OVEREXPRESSION; INVASION; ENHANCER; PROLIFERATION; CARCINOMA;
D O I
10.3892/or.2014.3459
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
MicroRNAs (miRNAs) are a class of small non-coding RNA molecules, which play regulatory roles at the post-transcriptional level by suppressing the translation of protein-coding genes or inducing mRNA cleavage. Dysregulated expression of miRNAs is involved in multiple types of cancers and plays important roles in regulating various biological processes including metastasis. miR-101 is downregulated in various types of cancer and functions as a suppressor of cell migration and invasion. Meanwhile, enhancer of zeste homolog 2 (EZH2) is associated with the metastatic potential of several aggressive tumors. In the present study, we reported that ectopic overexpression of miR-101 downregulated the expression level of EZH2 and significantly inhibited migration and invasion of osteosarcoma cells. In addition, knockdown of EZH2 by siRNA showed the same effect of miR-101 on migration and invasion. To conclude, these results indicate that miR-101 may act as a tumor suppressor in osteosarcoma, as it has a suppressive role in cell migration and invasion by targeting EZH2.
引用
收藏
页码:2143 / 2149
页数:7
相关论文
共 47 条
[1]
Increased risk for distant metastasis in patients with familial early-stage breast cancer and high EZH2 expression [J].
Alford, Sharon Hensley ;
Toy, Katherine ;
Merajver, Sofia D. ;
Kleer, Celina G. .
BREAST CANCER RESEARCH AND TREATMENT, 2012, 132 (02) :429-437
[2]
The tumor suppressor gene rap1GAP is silenced by miR-101-mediated EZH2 overexpression in invasive squamous cell carcinoma [J].
Banerjee, R. ;
Mani, R-S ;
Russo, N. ;
Scanlon, C. S. ;
Tsodikov, A. ;
Jing, X. ;
Cao, Q. ;
Palanisamy, N. ;
Metwally, T. ;
Inglehart, R. C. ;
Tomlins, S. ;
Bradford, C. ;
Carey, T. ;
Wolf, G. ;
Kalyana-Sundaram, S. ;
Chinnaiyan, A. M. ;
Varambally, S. ;
D'Silva, N. J. .
ONCOGENE, 2011, 30 (42) :4339-4349
[3]
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
[4]
Origins and Mechanisms of miRNAs and siRNAs [J].
Carthew, Richard W. ;
Sontheimer, Erik J. .
CELL, 2009, 136 (04) :642-655
[5]
Poorly differentiated synovial sarcoma is associated with high expression of enhancer of zeste homologue 2 (EZH2) [J].
Changchien, Yi-Che ;
Tatrai, Peter ;
Papp, Gergo ;
Sapi, Johanna ;
Fonyad, Laszlo ;
Szendroi, Miklos ;
Papai, Zsuzsanna ;
Sapi, Zoltan .
JOURNAL OF TRANSLATIONAL MEDICINE, 2012, 10
[6]
Dysregulation of MicroRNAs in cancer [J].
Chen, Pai-Sheng ;
Su, Jen-Liang ;
Hung, Mien-Chie .
JOURNAL OF BIOMEDICAL SCIENCE, 2012, 19
[7]
Establishment and characterization of human osteosarcoma cell lines with different pulmonary metastatic potentials [J].
Chen, Xiang ;
Yang, Tong-Tao ;
Wang, Wei ;
Sun, Hong-Hui ;
Ma, Bao-An ;
Li, Cun-Xiao ;
Ma, Qiong ;
Yu, Zhe ;
Fan, Qing-Yu .
CYTOTECHNOLOGY, 2009, 61 (1-2) :37-44
[8]
microRNA-101 inhibits lung cancer invasion through the regulation of enhancer of zeste homolog 2 [J].
Cho, Hyun Min ;
Jeon, Hyo Sung ;
Lee, Soo Young ;
Jeong, Kang Jin ;
Park, Soon-Young ;
Lee, Hoi Young ;
Lee, Jung Uee ;
Kim, Ji Hye ;
Kwon, Sun Jung ;
Choi, Eugene ;
Na, Moon Jun ;
Kang, Jaeku ;
Son, Ji Woong .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2011, 2 (05) :963-967
[9]
Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269
[10]
MicroRNA-145 targets vascular endothelial growth factor and inhibits invasion and metastasis of osteosarcoma cells [J].
Fan, Lei ;
Wu, Qiang ;
Xing, Xiaojuan ;
Wei, Yulong ;
Shao, Zengwu .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2012, 44 (05) :407-414