Cargando…

Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214

Nasopharyngeal carcinoma (NPC) is a distinct head and neck cancer, which is occurring at a high frequency in Southern China. Emerging studies have shown that long noncoding RNAs (lncRNAs) play a critical role in carcinogenesis and progression. In this study, we established a comprehensive lncRNA pro...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Jie, Ma, Jinqi, Zhao, Guosheng, Li, Guocai, Fu, Yunfeng, Luo, Yanwei, Gui, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cognizant Communication Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841018/
https://www.ncbi.nlm.nih.gov/pubmed/28245169
http://dx.doi.org/10.3727/096504017X14865126670075
_version_ 1783643707327643648
author Guo, Jie
Ma, Jinqi
Zhao, Guosheng
Li, Guocai
Fu, Yunfeng
Luo, Yanwei
Gui, Rong
author_facet Guo, Jie
Ma, Jinqi
Zhao, Guosheng
Li, Guocai
Fu, Yunfeng
Luo, Yanwei
Gui, Rong
author_sort Guo, Jie
collection PubMed
description Nasopharyngeal carcinoma (NPC) is a distinct head and neck cancer, which is occurring at a high frequency in Southern China. Emerging studies have shown that long noncoding RNAs (lncRNAs) play a critical role in carcinogenesis and progression. In this study, we established a comprehensive lncRNA profile in NPC and found that 35 lncRNAs were differentially expressed in NPC. We found that LINC0086 was decreased in NPC patient serum samples and tissues. The Kaplan–Meier survival curve showed that patients with high LINC0086 expression had a higher survival rate than those with low LINC0086 expression. LINC0086 expression was associated with NPC histological grade, lymph node metastasis, and clinical stage. Upregulation of LINC0086 inhibited cancer cell proliferation and promoted apoptosis. In addition, upregulation of LINC0086 dramatically decreased the expression of miR-214, an oncogene in several cancers, in C666-1 and HK-1 cells. An miR-214 binding site was found in the 3′-UTR of LINC0086. We also validated that both miR-214 and LINC0086 presented in the RISC complex, demonstrating that LINC0086 could decrease miR-214 expression by directly interacting with miR-214. Furthermore, the suppressive effects of LINC0086 on NPC cell growth were reversed by overexpression of miR-214 in vitro and in vivo. Thus, our study reports a novel mechanism underlying NPC carcinogenesis and provides a potential novel diagnosis and treatment biomarker for NPC.
format Online
Article
Text
id pubmed-7841018
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Cognizant Communication Corporation
record_format MEDLINE/PubMed
spelling pubmed-78410182021-02-16 Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214 Guo, Jie Ma, Jinqi Zhao, Guosheng Li, Guocai Fu, Yunfeng Luo, Yanwei Gui, Rong Oncol Res Article Nasopharyngeal carcinoma (NPC) is a distinct head and neck cancer, which is occurring at a high frequency in Southern China. Emerging studies have shown that long noncoding RNAs (lncRNAs) play a critical role in carcinogenesis and progression. In this study, we established a comprehensive lncRNA profile in NPC and found that 35 lncRNAs were differentially expressed in NPC. We found that LINC0086 was decreased in NPC patient serum samples and tissues. The Kaplan–Meier survival curve showed that patients with high LINC0086 expression had a higher survival rate than those with low LINC0086 expression. LINC0086 expression was associated with NPC histological grade, lymph node metastasis, and clinical stage. Upregulation of LINC0086 inhibited cancer cell proliferation and promoted apoptosis. In addition, upregulation of LINC0086 dramatically decreased the expression of miR-214, an oncogene in several cancers, in C666-1 and HK-1 cells. An miR-214 binding site was found in the 3′-UTR of LINC0086. We also validated that both miR-214 and LINC0086 presented in the RISC complex, demonstrating that LINC0086 could decrease miR-214 expression by directly interacting with miR-214. Furthermore, the suppressive effects of LINC0086 on NPC cell growth were reversed by overexpression of miR-214 in vitro and in vivo. Thus, our study reports a novel mechanism underlying NPC carcinogenesis and provides a potential novel diagnosis and treatment biomarker for NPC. Cognizant Communication Corporation 2017-08-07 /pmc/articles/PMC7841018/ /pubmed/28245169 http://dx.doi.org/10.3727/096504017X14865126670075 Text en Copyright © 2017 Cognizant, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under a Creative Commons Attribution-NonCommercial NoDerivatives 4.0 International License.
spellingShingle Article
Guo, Jie
Ma, Jinqi
Zhao, Guosheng
Li, Guocai
Fu, Yunfeng
Luo, Yanwei
Gui, Rong
Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214
title Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214
title_full Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214
title_fullStr Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214
title_full_unstemmed Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214
title_short Long Noncoding RNA LINC0086 Functions as a Tumor Suppressor in Nasopharyngeal Carcinoma by Targeting miR-214
title_sort long noncoding rna linc0086 functions as a tumor suppressor in nasopharyngeal carcinoma by targeting mir-214
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7841018/
https://www.ncbi.nlm.nih.gov/pubmed/28245169
http://dx.doi.org/10.3727/096504017X14865126670075
work_keys_str_mv AT guojie longnoncodingrnalinc0086functionsasatumorsuppressorinnasopharyngealcarcinomabytargetingmir214
AT majinqi longnoncodingrnalinc0086functionsasatumorsuppressorinnasopharyngealcarcinomabytargetingmir214
AT zhaoguosheng longnoncodingrnalinc0086functionsasatumorsuppressorinnasopharyngealcarcinomabytargetingmir214
AT liguocai longnoncodingrnalinc0086functionsasatumorsuppressorinnasopharyngealcarcinomabytargetingmir214
AT fuyunfeng longnoncodingrnalinc0086functionsasatumorsuppressorinnasopharyngealcarcinomabytargetingmir214
AT luoyanwei longnoncodingrnalinc0086functionsasatumorsuppressorinnasopharyngealcarcinomabytargetingmir214
AT guirong longnoncodingrnalinc0086functionsasatumorsuppressorinnasopharyngealcarcinomabytargetingmir214