| Literature DB >> 25213660 |
Ming-zhe Ma1,2, Xiang Kong3,4, Ming-zhe Weng1, Ming-di Zhang1, Yi-yu Qin1, Wei Gong1, Wen-jie Zhang1, Zhi-wei Quan1.
Abstract
The identification of cancer-associated long non-coding RNAs (lncRNAs) and the investigation of their molecular and biological functions are vital for understanding the molecular biology and progression of cancer. The lncRNA-LET, a newly identified lncRNA, was demonstrated to be down-regulated in hepatocellular cancer. However, little is known about its role in gallbladder cancer. In the present study, an obvious down-regulation of lncRNA-LET was observed in gallbladder cancer compared to their adjacent normal tissues. Meanwhile, patients with low expression of lncRNA-LET have significantly poorer prognosis than those with high expression. We confirmed that hypoxia decreased lncRNA-LET levels in gallbladder cancer cells. Moreover, lncRNA-LET overexpression was further validated to inhibit the invasion of gallbladder cancer cells under hypoxic or normoxic conditions in vitro. We demonstrated that lncRNA-LET overexpression conferred a proliferative advantage to tumor cells under hypoxic conditions. The ectopic expression of lncRNA-LET led to the promotion of cell cycle arrest at G0/G1 phase and to the induction of apoptosis under hypoxic conditions. Ectopic expression of LncRNA-LET also suppressed gallbladder tumor growth in vivo. Our findings indicate that lncRNA-LET may represent a prognostic marker and a potential therapeutic target for gallbladder cancer.Entities:
Keywords: gallbladder cancer; hypoxia; lncRNA-LET; long non-coding RNA; prognosis
Mesh:
Substances:
Year: 2014 PMID: 25213660 DOI: 10.1002/mc.22215
Source DB: PubMed Journal: Mol Carcinog ISSN: 0899-1987 Impact factor: 4.784