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nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer
nc886 is a 101 nucleotide long non-coding RNA that has been designated as a precursor microRNA or a vault RNA based upon it sequence. nc886 has also been suggested to be a tumor suppressor, mainly inferred by its expression pattern as well as its genomic location at human chromosome 5q31, a locus fo...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116533/ https://www.ncbi.nlm.nih.gov/pubmed/25003254 |
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author | Lee, Kwang-Soo Park, Jong-Lyul Lee, Kwanbok Richardson, Lauren E. Johnson, Betty H. Lee, Hyun-Sung Lee, Ju-Seog Kim, Sang-Bae Kwon, Oh-Hyung Song, Kyu Sang Kim, Yong Sung Ashktorab, Hassan Smoot, Duane T. Jeon, Sung Ho Kim, Seon-Young Lee, Yong Sun |
author_facet | Lee, Kwang-Soo Park, Jong-Lyul Lee, Kwanbok Richardson, Lauren E. Johnson, Betty H. Lee, Hyun-Sung Lee, Ju-Seog Kim, Sang-Bae Kwon, Oh-Hyung Song, Kyu Sang Kim, Yong Sung Ashktorab, Hassan Smoot, Duane T. Jeon, Sung Ho Kim, Seon-Young Lee, Yong Sun |
author_sort | Lee, Kwang-Soo |
collection | PubMed |
description | nc886 is a 101 nucleotide long non-coding RNA that has been designated as a precursor microRNA or a vault RNA based upon it sequence. nc886 has also been suggested to be a tumor suppressor, mainly inferred by its expression pattern as well as its genomic location at human chromosome 5q31, a locus for a tumor suppressor gene(s). However, legitimate data based on nc886's correct identity for its functional cellular roles as a tumor suppressor have not been provided yet. Here we have investigated nc886 in gastric cancer where its expression is suppressed due to CpG DNA hypermethylation at its promoter region in a cohort of paired tumor/normal tissues from 88 gastric cancer patients. CpG hypermethylation of nc886 and thus its diminished expression is significantly associated with poor survival in these cancer patients. nc886 inhibits cell proliferation when ectopically expressed in gastric cancer cells. nc886's tumor suppressive role is corroborated by the induction of well-known oncogenes such as FOS, NF-κB, and MYC upon its knockdown. All these activities of nc886 are undoubtedly independent of mature microRNA or vault RNA. Our data indicate that nc886 is a putative tumor suppressor and could potentially be used as a diagnostic marker in gastric cancer. |
format | Online Article Text |
id | pubmed-4116533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41165332014-08-04 nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer Lee, Kwang-Soo Park, Jong-Lyul Lee, Kwanbok Richardson, Lauren E. Johnson, Betty H. Lee, Hyun-Sung Lee, Ju-Seog Kim, Sang-Bae Kwon, Oh-Hyung Song, Kyu Sang Kim, Yong Sung Ashktorab, Hassan Smoot, Duane T. Jeon, Sung Ho Kim, Seon-Young Lee, Yong Sun Oncotarget Research Paper nc886 is a 101 nucleotide long non-coding RNA that has been designated as a precursor microRNA or a vault RNA based upon it sequence. nc886 has also been suggested to be a tumor suppressor, mainly inferred by its expression pattern as well as its genomic location at human chromosome 5q31, a locus for a tumor suppressor gene(s). However, legitimate data based on nc886's correct identity for its functional cellular roles as a tumor suppressor have not been provided yet. Here we have investigated nc886 in gastric cancer where its expression is suppressed due to CpG DNA hypermethylation at its promoter region in a cohort of paired tumor/normal tissues from 88 gastric cancer patients. CpG hypermethylation of nc886 and thus its diminished expression is significantly associated with poor survival in these cancer patients. nc886 inhibits cell proliferation when ectopically expressed in gastric cancer cells. nc886's tumor suppressive role is corroborated by the induction of well-known oncogenes such as FOS, NF-κB, and MYC upon its knockdown. All these activities of nc886 are undoubtedly independent of mature microRNA or vault RNA. Our data indicate that nc886 is a putative tumor suppressor and could potentially be used as a diagnostic marker in gastric cancer. Impact Journals LLC 2014-05-31 /pmc/articles/PMC4116533/ /pubmed/25003254 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, Kwang-Soo Park, Jong-Lyul Lee, Kwanbok Richardson, Lauren E. Johnson, Betty H. Lee, Hyun-Sung Lee, Ju-Seog Kim, Sang-Bae Kwon, Oh-Hyung Song, Kyu Sang Kim, Yong Sung Ashktorab, Hassan Smoot, Duane T. Jeon, Sung Ho Kim, Seon-Young Lee, Yong Sun nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer |
title | nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer |
title_full | nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer |
title_fullStr | nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer |
title_full_unstemmed | nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer |
title_short | nc886, a non-coding RNA of anti-proliferative role, is suppressed by CpG DNA methylation in human gastric cancer |
title_sort | nc886, a non-coding rna of anti-proliferative role, is suppressed by cpg dna methylation in human gastric cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116533/ https://www.ncbi.nlm.nih.gov/pubmed/25003254 |
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