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Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression

Evidence indicates that long non-coding RNAs (lncRNAs) play a critical role in the regulation of tumor cellular processes, such as proliferation, apoptosis, and metastasis. LncRNA CRNDE (Colorectal Neoplasia Differentially Expressed) is located at human chromosome 16 and has been found overexpressed...

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Autores principales: Ding, Jie, Li, Juan, Wang, HaiYan, Tian, Yun, Xie, Min, He, XueZhi, Ji, Hao, Ma, Zhonghua, Hui, Bingqing, Wang, Keming, Ji, Guozhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596537/
https://www.ncbi.nlm.nih.gov/pubmed/28796262
http://dx.doi.org/10.1038/cddis.2017.328
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author Ding, Jie
Li, Juan
Wang, HaiYan
Tian, Yun
Xie, Min
He, XueZhi
Ji, Hao
Ma, Zhonghua
Hui, Bingqing
Wang, Keming
Ji, Guozhong
author_facet Ding, Jie
Li, Juan
Wang, HaiYan
Tian, Yun
Xie, Min
He, XueZhi
Ji, Hao
Ma, Zhonghua
Hui, Bingqing
Wang, Keming
Ji, Guozhong
author_sort Ding, Jie
collection PubMed
description Evidence indicates that long non-coding RNAs (lncRNAs) play a critical role in the regulation of tumor cellular processes, such as proliferation, apoptosis, and metastasis. LncRNA CRNDE (Colorectal Neoplasia Differentially Expressed) is located at human chromosome 16 and has been found overexpressed in a variety of cancers including colorectal cancer (CRC). In this paper, we report that lncRNA CRNDE expression was remarkably upregulated in CRC tissues and that lncRNA CRNDE overexpression was positively correlated with advanced pathological stages and larger tumor sizes. In addition, the knockdown of CRNDE significantly suppressed proliferation and caused apoptosis of CRC cells both in vitro and in vivo. Furthermore, RNA immunoprecipitation and chromatin immunoprecipitation assays demonstrated that lncRNA CRNDE could epigenetically suppress the expressions of dual-specificity phosphatase 5 (DUSP5) and CDKN1A by binding to EZH2 (the key components of Polycomb repressive complex 2 (PRC2)), thus promoting CRC development. In conclusion, our data suggest that the lncRNA CRNDE promotes the progression of CRC and is a potential therapeutic target for CRC intervention.
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spelling pubmed-55965372017-09-14 Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression Ding, Jie Li, Juan Wang, HaiYan Tian, Yun Xie, Min He, XueZhi Ji, Hao Ma, Zhonghua Hui, Bingqing Wang, Keming Ji, Guozhong Cell Death Dis Original Article Evidence indicates that long non-coding RNAs (lncRNAs) play a critical role in the regulation of tumor cellular processes, such as proliferation, apoptosis, and metastasis. LncRNA CRNDE (Colorectal Neoplasia Differentially Expressed) is located at human chromosome 16 and has been found overexpressed in a variety of cancers including colorectal cancer (CRC). In this paper, we report that lncRNA CRNDE expression was remarkably upregulated in CRC tissues and that lncRNA CRNDE overexpression was positively correlated with advanced pathological stages and larger tumor sizes. In addition, the knockdown of CRNDE significantly suppressed proliferation and caused apoptosis of CRC cells both in vitro and in vivo. Furthermore, RNA immunoprecipitation and chromatin immunoprecipitation assays demonstrated that lncRNA CRNDE could epigenetically suppress the expressions of dual-specificity phosphatase 5 (DUSP5) and CDKN1A by binding to EZH2 (the key components of Polycomb repressive complex 2 (PRC2)), thus promoting CRC development. In conclusion, our data suggest that the lncRNA CRNDE promotes the progression of CRC and is a potential therapeutic target for CRC intervention. Nature Publishing Group 2017-08 2017-08-10 /pmc/articles/PMC5596537/ /pubmed/28796262 http://dx.doi.org/10.1038/cddis.2017.328 Text en Copyright © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ Cell Death and Disease is an open-access journal published by Nature Publishing Group. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Ding, Jie
Li, Juan
Wang, HaiYan
Tian, Yun
Xie, Min
He, XueZhi
Ji, Hao
Ma, Zhonghua
Hui, Bingqing
Wang, Keming
Ji, Guozhong
Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression
title Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression
title_full Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression
title_fullStr Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression
title_full_unstemmed Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression
title_short Long noncoding RNA CRNDE promotes colorectal cancer cell proliferation via epigenetically silencing DUSP5/CDKN1A expression
title_sort long noncoding rna crnde promotes colorectal cancer cell proliferation via epigenetically silencing dusp5/cdkn1a expression
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596537/
https://www.ncbi.nlm.nih.gov/pubmed/28796262
http://dx.doi.org/10.1038/cddis.2017.328
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