Cargando…
Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis
nc886 (= vtRNA2-1 or pre-miR-886) is a recently discovered noncoding RNA that is a cellular PKR (Protein Kinase RNA-activated) ligand and repressor. nc886 has been suggested to be a tumor suppressor, solely based on its expression pattern and genomic locus. In this report, we have provided sufficien...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116496/ https://www.ncbi.nlm.nih.gov/pubmed/25004084 |
_version_ | 1782328603665498112 |
---|---|
author | Lee, Hyun-Sung Lee, Kwanbok Jang, Hee-Jin Lee, Geon Kook Park, Jong-Lyul Kim, Seon-Young Kim, Sang-Bae Johnson, Betty H. Zo, Jae Ill Lee, Ju-Seog Lee, Yong Sun |
author_facet | Lee, Hyun-Sung Lee, Kwanbok Jang, Hee-Jin Lee, Geon Kook Park, Jong-Lyul Kim, Seon-Young Kim, Sang-Bae Johnson, Betty H. Zo, Jae Ill Lee, Ju-Seog Lee, Yong Sun |
author_sort | Lee, Hyun-Sung |
collection | PubMed |
description | nc886 (= vtRNA2-1 or pre-miR-886) is a recently discovered noncoding RNA that is a cellular PKR (Protein Kinase RNA-activated) ligand and repressor. nc886 has been suggested to be a tumor suppressor, solely based on its expression pattern and genomic locus. In this report, we have provided sufficient evidence that nc886 is a putative tumor suppressor in esophageal squamous cell carcinoma (ESCC). In 84 paired specimens from ESCC patients, nc886 expression is significantly lower in tumors than their normal adjacent tissues. More importantly, decreased expression of nc886 is significantly associated with shorter recurrence-free survival of the patients. Suppression of nc886 is mediated by CpG hypermethylation of its promoter, as evidenced by its significant negative correlation to nc886 expression in ESCC tumors and by induced expression of nc886 upon demethylation of its promoter. Knockdown of nc886 and consequent PKR activation induce FOS and MYC oncogenes as well as some inflammatory genes including oncogenic NF-κB. When ectopically expressed, nc886 inhibits proliferation of ESCC cells, further demonstrating that nc886 could be a tumor suppressor. All these findings implicate nc886 as a novel, putative tumor suppressor that is epigenetically silenced and regulates the expression of oncogenes in ESCC. |
format | Online Article Text |
id | pubmed-4116496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41164962014-08-04 Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis Lee, Hyun-Sung Lee, Kwanbok Jang, Hee-Jin Lee, Geon Kook Park, Jong-Lyul Kim, Seon-Young Kim, Sang-Bae Johnson, Betty H. Zo, Jae Ill Lee, Ju-Seog Lee, Yong Sun Oncotarget Research Paper nc886 (= vtRNA2-1 or pre-miR-886) is a recently discovered noncoding RNA that is a cellular PKR (Protein Kinase RNA-activated) ligand and repressor. nc886 has been suggested to be a tumor suppressor, solely based on its expression pattern and genomic locus. In this report, we have provided sufficient evidence that nc886 is a putative tumor suppressor in esophageal squamous cell carcinoma (ESCC). In 84 paired specimens from ESCC patients, nc886 expression is significantly lower in tumors than their normal adjacent tissues. More importantly, decreased expression of nc886 is significantly associated with shorter recurrence-free survival of the patients. Suppression of nc886 is mediated by CpG hypermethylation of its promoter, as evidenced by its significant negative correlation to nc886 expression in ESCC tumors and by induced expression of nc886 upon demethylation of its promoter. Knockdown of nc886 and consequent PKR activation induce FOS and MYC oncogenes as well as some inflammatory genes including oncogenic NF-κB. When ectopically expressed, nc886 inhibits proliferation of ESCC cells, further demonstrating that nc886 could be a tumor suppressor. All these findings implicate nc886 as a novel, putative tumor suppressor that is epigenetically silenced and regulates the expression of oncogenes in ESCC. Impact Journals LLC 2014-04-27 /pmc/articles/PMC4116496/ /pubmed/25004084 Text en Copyright: © 2014 Lee et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Lee, Hyun-Sung Lee, Kwanbok Jang, Hee-Jin Lee, Geon Kook Park, Jong-Lyul Kim, Seon-Young Kim, Sang-Bae Johnson, Betty H. Zo, Jae Ill Lee, Ju-Seog Lee, Yong Sun Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis |
title | Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis |
title_full | Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis |
title_fullStr | Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis |
title_full_unstemmed | Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis |
title_short | Epigenetic silencing of the non-coding RNA nc886 provokes oncogenes during human esophageal tumorigenesis |
title_sort | epigenetic silencing of the non-coding rna nc886 provokes oncogenes during human esophageal tumorigenesis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116496/ https://www.ncbi.nlm.nih.gov/pubmed/25004084 |
work_keys_str_mv | AT leehyunsung epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT leekwanbok epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT jangheejin epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT leegeonkook epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT parkjonglyul epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT kimseonyoung epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT kimsangbae epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT johnsonbettyh epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT zojaeill epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT leejuseog epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis AT leeyongsun epigeneticsilencingofthenoncodingrnanc886provokesoncogenesduringhumanesophagealtumorigenesis |