Li Enqi, Zhang Jinli, Yuan Tianxiang, Ma Baotong
Department of Orthopaedic Trauma, TianJin Hospital, Jiefang Road No. 406, Hexi District, 300211, Tianjin, China,
Tumour Biol. 2014 Aug;35(8):7645-50. doi: 10.1007/s13277-014-2031-9. Epub 2014 May 7.
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.
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。