MicroRNA-21 is involved in osteosarcoma cell invasion and migration

被引:149
作者
Wu Ziyan [1 ]
Yang Shuhua [1 ]
Weng Xiufang [2 ]
Liu Xiaoyun [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Union Hosp, Dept Orthoped, Wuhan 430022, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Immunol, Wuhan 430022, Peoples R China
基金
中国国家自然科学基金;
关键词
Osteosarcoma; miR-21; Invasion; Migration; RECK; TUMOR-SUPPRESSOR GENE; EXPRESSION; IDENTIFICATION; TARGETS; CANCER;
D O I
10.1007/s12032-010-9563-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs are involved in different cancer-related processes. MicroRNA-21 (miR-21), as an oncomiR, is overexpressed in all kinds of tumors and the role of miR-21 in carcinogenesis is elucidated in many cancers gradually. However, the function of miR-21 in osteosarcoma is still unclear. In our study, we found that miR-21 was significantly overexpressed in osteosarcoma tissues. More importantly, we confirmed that knockdown of miR-21 greatly decreased cell invasion and migration of MG-63. Furthermore, we identified that RECK (reversion-inducing-cysteine-rich protein with kazal motifs), a tumor suppressor gene, was a direct target of miR-21. Finally, the expression of RECK protein negatively correlated with the expression of miR-21 in human osteosarcoma tissues, indicating the potential regulation of RECK by miR-21. Our results suggest that miR-21 expression has a key role in regulating cellular processes in osteosarcoma, likely through regulating RECK and may serve as a therapeutic target.
引用
收藏
页码:1469 / 1474
页数:6
相关论文
共 26 条
[1]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[2]   MicroRNA-21 (miR-21) post-transcriptionally downregulates tumor suppressor Pdcd4 and stimulates invasion, intravasation and metastasis in colorectal cancer [J].
Asangani, I. A. ;
Rasheed, S. A. K. ;
Nikolova, D. A. ;
Leupold, J. H. ;
Colburn, N. H. ;
Post, S. ;
Allgayer, H. .
ONCOGENE, 2008, 27 (15) :2128-2136
[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]   Identification of hundreds of conserved and nonconserved human microRNAs [J].
Bentwich, I ;
Avniel, A ;
Karov, Y ;
Aharonov, R ;
Gilad, S ;
Barad, O ;
Barzilai, A ;
Einat, P ;
Einav, U ;
Meiri, E ;
Sharon, E ;
Spector, Y ;
Bentwich, Z .
NATURE GENETICS, 2005, 37 (07) :766-770
[5]   Phylogenetic shadowing and computational identification of human microRNA genes [J].
Berezikov, E ;
Guryev, V ;
van de Belt, J ;
Wienholds, E ;
Plasterk, RHA ;
Cuppen, E .
CELL, 2005, 120 (01) :21-24
[6]   MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells [J].
Chan, JA ;
Krichevsky, AM ;
Kosik, KS .
CANCER RESEARCH, 2005, 65 (14) :6029-6033
[7]   MicroRNA-21 knockdown disrupts glioma growth In vivo and displays synergistic cytotoxicity with neural precursor cell-delivered S-TRAIL in human gliomas [J].
Corsten, Maarten F. ;
Miranda, Rafael ;
Kasmieh, Randa ;
Krichevsky, Anna M. ;
Weissleder, Ralph ;
Shah, Khalid .
CANCER RESEARCH, 2007, 67 (19) :8994-9000
[8]   Sequence variations of microRNAs in human cancer: Alterations in predicted secondary structure do not affect processing [J].
Diederichs, Sven ;
Haber, Daniel A. .
CANCER RESEARCH, 2006, 66 (12) :6097-6104
[9]   MicroRNA 21 promotes glioma invasion by targeting matrix metalloproteinase regulators [J].
Gabriely, Galina ;
Wurdinger, Thomas ;
Kesari, Santosh ;
Esau, Christine C. ;
Burchard, Julja ;
Linsley, Peter S. ;
Krichevsky, Anna M. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (17) :5369-5380
[10]   MicroRNAs in cell proliferation, cell death, and tumorigenesis [J].
Hwang, HW ;
Mendell, JT .
BRITISH JOURNAL OF CANCER, 2006, 94 (06) :776-780