| Literature DB >> 30026052 |
Yun Wang1, Xiaojie Zhang1, Zhi Wang1, Qinchao Hu1, Jie Wu1, Yuanyuan Li1, Xianyue Ren1, Tong Wu1, Xiaoan Tao1, Xiaobing Chen1, Xiaoxu Li1, Juan Xia2, Bin Cheng3.
Abstract
The dysregulation of glycolysis has been suggested to lead to alteration of cell drug resistance signals, proliferation and metastasis. Emerging evidence indicates that lncRNAs play a key role in the cellular processes of tumor cells, including glycolysis, growth, and movement. However, the role and potential mechanism of lncRNAs in glycolysis-mediated metastasis has not been explored. In this study, we identified a novel lncRNA lnc-p23154 which is associated with OSCC patient metastasis and the promotion of OSCC cell migration and invasion in vitro and in vivo. Furthermore, we found that lnc-p23154 also participates in OSCC glycolysis by facilitating Glut1 expression. Rescue of lnc-p23154 reversed the suppression of OSCC cell migration and invasion induced by Glut1 knockdown. In addition, lnc-p23154 is mainly located in the nucleus and binds to the promoter region of miR-378a-3p, which represses Glut1 expression by targeting to its 3'UTR directly. Therefore, we concluded that lnc-p23154 may play an important role in Glut1-mediated glycolysis by inhibiting miR-378a-3p transcription and accelerate OSCC metastasis.Entities:
Keywords: Glut1; Glycolysis; Long non-coding RNA; Metastasis; Oral squamous cell carcinoma (OSCC)
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Year: 2018 PMID: 30026052 DOI: 10.1016/j.canlet.2018.07.016
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679