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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
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