| Literature DB >> 24604520 |
Huawei Jiang1, Dasong Hua2, Jing Zhang2, Qing Lan3, Qiang Huang3, Jae-Geun Yoon4, Xu Han2, Lisha Li2, Gregory Foltz4, Shu Zheng1, Biaoyang Lin1.
Abstract
MicroRNAs (miRNAs) are small non-coding RNAs of 20-25 nucleotides in length that are capable of modulating gene expression post-transcriptionally. The potential roles of miRNAs in the tumorigenesis of glioblastoma (GBM) have been under intensive studies in the past few years. In the present study, we found a positive correlation between the levels of miR-127-3p and the cell migration and invasion abilities in several human GBM cell lines. We showed that miR-127-3p promoted cell migration and invasion of GBM cells using in vitro cell lines and in vivo mouse models. We identified SEPT7, a known tumor-suppressor gene that has been reported to suppress GBM cell migration and invasion, as a direct target of miR-127-3p. SEPT7 was able to partially abrogate the effect of miR-127-3p on cell migration and invasion. In addition, microarray analysis revealed that miR-127-3p regulated a number of migration and invasion-related genes. Finally, we verified that miR-127-3p affected the remodeling of the actin cytoskeleton mediated by SEPT7 in GBM cells.Entities:
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Year: 2014 PMID: 24604520 DOI: 10.3892/or.2014.3055
Source DB: PubMed Journal: Oncol Rep ISSN: 1021-335X Impact factor: 3.906