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微小RNA-145通过靶向ROCK1抑制骨肉瘤细胞的增殖和侵袭。

MiR-145 inhibits osteosarcoma cells proliferation and invasion by targeting ROCK1.

作者信息

Li Enqi, Zhang Jinli, Yuan Tianxiang, Ma Baotong

机构信息

Department of Orthopaedic Trauma, TianJin Hospital, Jiefang Road No. 406, Hexi District, 300211, Tianjin, China,

出版信息

Tumour Biol. 2014 Aug;35(8):7645-50. doi: 10.1007/s13277-014-2031-9. Epub 2014 May 7.

Abstract

MicroRNAs (miRNAs) contribute to the development and progression of various types of human cancers. The aim of this study was to study the role of miR-145 and to identify its functional target gene in osteosarcoma (OS) cells. We found that miR-145 was reduced in OS tissues and cell lines. Enforced expression of miR-145 inhibited cell proliferation, migration, and invasion abilities of MG-63 cells. Furthermore, we revealed that Rho-associated protein kinase 1 (ROCK1) was a target of miR-145 in OS. Finally, we found that silencing of ROCK1 performed similar effects with miR-145 in MG-63 cells, and ROCK1 was inversely correlated with miR-145 in OS tissues. Collectively, these data indicate that miR-145 may act as a tumor suppressor and contributes to the progression of OS through targeting ROCK1.

摘要

微小RNA(miRNA)在多种人类癌症的发生和发展过程中发挥作用。本研究旨在探讨miR-145在骨肉瘤(OS)细胞中的作用,并鉴定其功能靶基因。我们发现miR-145在OS组织和细胞系中表达降低。过表达miR-145可抑制MG-63细胞的增殖、迁移和侵袭能力。此外,我们发现Rho相关蛋白激酶1(ROCK1)是OS中miR-145的靶基因。最后,我们发现沉默ROCK1在MG-63细胞中产生与miR-145相似的效应,且在OS组织中ROCK1与miR-145呈负相关。综上所述,这些数据表明miR-145可能作为一种肿瘤抑制因子,通过靶向ROCK1促进OS的进展。

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