Department of Orthopaedics, Sheng Jing Hospital of China Medical University, Shenyang, 110004, Liaoning, People's Republic of China.
Mol Cell Biochem. 2013 Dec;384(1-2):105-11. doi: 10.1007/s11010-013-1786-4. Epub 2013 Aug 22.
Accumulating evidence has shown that microRNAs are involved in multiple processes in cancer development and progression. Recently, miR-335 has been identified as a tumor-suppressing microRNA in many human cancers. However, the specific function of miR-335 in osteosarcoma is unclear at this point. In this study, we found that the expression of miR-335 in osteosarcoma tissues and cell lines was much lower than that in normal control, respectively, and the downregulated miR-335 was significantly associated with lymph-node metastasis. Transfection of miR-335 mimics could significantly inhibit the cell migration and invasion in MG-63 and U2OS osteosarcoma cell lines. Moreover, we also showed that ROCK1 was negatively regulated by miR-335 at the posttranscriptional level, via a specific target site within the 3'UTR by luciferase reporter assay. The expression of ROCK1 was inversely correlated with miR-335 expression in osteosarcoma tissues, and knockdown of ROCK1 by siRNA-inhibited osteosarcoma cells migration and invasion resembling that of miR-335 overexpression. Thus, our findings suggest that miR-335 acts as tumor suppressor by targeting the ROCK1 gene and inhibiting osteosarcoma cells migration and invasion. The findings of this study contribute to current understanding of the functions of miR-335 in osteosarcoma.
越来越多的证据表明,microRNAs 参与了癌症发展和进展的多个过程。最近,miR-335 已被确定为许多人类癌症中的肿瘤抑制 microRNA。然而,miR-335 在骨肉瘤中的具体功能目前尚不清楚。在这项研究中,我们发现 miR-335 在骨肉瘤组织和细胞系中的表达明显低于正常对照,下调的 miR-335 与淋巴结转移显著相关。miR-335 模拟物的转染可显著抑制 MG-63 和 U2OS 骨肉瘤细胞系的细胞迁移和侵袭。此外,我们还通过荧光素酶报告基因检测显示,ROCK1 在转录后水平上被 miR-335 负调控,通过 3'UTR 中的特定靶位。ROCK1 的表达与骨肉瘤组织中 miR-335 的表达呈负相关,siRNA 敲低 ROCK1 抑制骨肉瘤细胞迁移和侵袭,类似于 miR-335 的过表达。因此,我们的研究结果表明,miR-335 通过靶向 ROCK1 基因抑制骨肉瘤细胞迁移和侵袭,发挥肿瘤抑制作用。本研究的结果有助于了解 miR-335 在骨肉瘤中的功能。