Maskey Niraj, Li Dengfeng, Xu Hui, Song Hongming, Wu Chenyang, Hua Kaiyao, Song Jialu, Fang Lin
Department of Thyroid and Breast Surgery, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai 200072, P.R. China.
Oncol Lett. 2017 Aug;14(2):2261-2267. doi: 10.3892/ol.2017.6439. Epub 2017 Jun 21.
MicroRNAs (miRNAs/miRs) are 19-25 nucleotide-long, non-coding RNAs that regulate the expression of target genes at the post-transcriptional level. In the present study, the role of miR-340 in breast cancer (BC) was investigated. The overexpression of miR-340 significantly inhibited the proliferation, migration and invasion of human breast MDA-MB-231 cancer cells . The Rho-associated, coiled-coil containing protein kinase 1 (ROCK1) gene was identified as a target of miR-340; its expression was downregulated by overexpression of miR-340 by binding to its 3'-untranslated region. The short interfering RNA-mediated silencing of ROCK1 was also performed, which phenocopied the effects of miR-340 overexpression. An inhibitor of miR-340 was used to suppress miR-340 expression, which led to increased expression of ROCK1, thus improving the proliferation, migration and invasion of MDA-MB-231 cells. Data from the present study suggest that miR-340 inhibits MDA-MB-231 cell growth and its downregulation may lead to the progression and metastasis of BC. Thus, miR340 may act as a tumor-suppressor agent that could serve a key role in the diagnosis and therapy of BC.
微小RNA(miRNA/miR)是长度为19 - 25个核苷酸的非编码RNA,其在转录后水平调节靶基因的表达。在本研究中,对miR - 340在乳腺癌(BC)中的作用进行了研究。miR - 340的过表达显著抑制了人乳腺MDA - MB - 231癌细胞的增殖、迁移和侵袭。含Rho相关卷曲螺旋的蛋白激酶1(ROCK1)基因被鉴定为miR - 340的靶标;通过与ROCK1基因的3'非翻译区结合,miR - 340的过表达下调了其表达。还进行了短干扰RNA介导的ROCK1基因沉默,其模拟了miR - 340过表达的效果。使用miR - 340抑制剂抑制miR - 340表达,这导致ROCK1表达增加,从而促进了MDA - MB - 231细胞的增殖、迁移和侵袭。本研究数据表明,miR - 340抑制MDA - MB - 231细胞生长,其下调可能导致BC的进展和转移。因此,miR340可能作为一种肿瘤抑制因子,在BC的诊断和治疗中发挥关键作用。