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Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation

Long non‐coding RNAs (lncRNAs) have potential applications in clinical diagnosis and targeted cancer therapies. However, the expression profile of lncRNAs in colorectal cancer (CRC) initiation is still unclear. In this study, the expression profiles of lncRNAs and mRNAs were determined by microarray...

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Autores principales: Dai, Lei, Li, Junshu, Dong, Zhexu, Liu, Yi, Chen, Ye, Chen, Na, Cheng, Lin, Fang, Chao, Wang, Huiling, Ji, Yanhong, Chen, Shuang, Su, Xiaolan, Shi, Gang, Lin, Yi, Zhang, Shuang, Yang, Yang, Qiu, Meng, Yu, Dechao, Huang, Wei, Zhou, Zongguang, Wei, Yuquan, Deng, Hongxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533480/
https://www.ncbi.nlm.nih.gov/pubmed/30920116
http://dx.doi.org/10.1111/jcmm.14300
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author Dai, Lei
Li, Junshu
Dong, Zhexu
Liu, Yi
Chen, Ye
Chen, Na
Cheng, Lin
Fang, Chao
Wang, Huiling
Ji, Yanhong
Chen, Shuang
Su, Xiaolan
Shi, Gang
Lin, Yi
Zhang, Shuang
Yang, Yang
Qiu, Meng
Yu, Dechao
Huang, Wei
Zhou, Zongguang
Wei, Yuquan
Deng, Hongxin
author_facet Dai, Lei
Li, Junshu
Dong, Zhexu
Liu, Yi
Chen, Ye
Chen, Na
Cheng, Lin
Fang, Chao
Wang, Huiling
Ji, Yanhong
Chen, Shuang
Su, Xiaolan
Shi, Gang
Lin, Yi
Zhang, Shuang
Yang, Yang
Qiu, Meng
Yu, Dechao
Huang, Wei
Zhou, Zongguang
Wei, Yuquan
Deng, Hongxin
author_sort Dai, Lei
collection PubMed
description Long non‐coding RNAs (lncRNAs) have potential applications in clinical diagnosis and targeted cancer therapies. However, the expression profile of lncRNAs in colorectal cancer (CRC) initiation is still unclear. In this study, the expression profiles of lncRNAs and mRNAs were determined by microarray at specific tumour stages in an AOM/DSS‐induced primary colon cancer model. The temporal expression of lncRNAs was analysed by K‐means clustering. Additionally, weighted correlation network analysis (WGCNA) and gene ontology analysis were performed to construct co‐expression networks and establish functions of the identified lncRNAs and mRNAs. Our results suggested that 4307 lncRNAs and 5798 mRNAs are deregulated during CRC initiation. These differential expression genes (DEGs) exhibited a clear correlation with the differential stage of tumour initiation. WGCNA results suggested that a series of hub lncRNAs are involved in regulating cell stemness, colon inflammation, oxidative stress response and cell death at each stage. Among them, lncRNA H19 was up‐regulated in colon tumours and correlated with poor patient prognosis. Collectively, we have been the first to demonstrate the temporal expression and function of lncRNAs in CRC initiation. These results provide novel diagnosis and therapy targets for CRC.
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spelling pubmed-65334802019-06-01 Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation Dai, Lei Li, Junshu Dong, Zhexu Liu, Yi Chen, Ye Chen, Na Cheng, Lin Fang, Chao Wang, Huiling Ji, Yanhong Chen, Shuang Su, Xiaolan Shi, Gang Lin, Yi Zhang, Shuang Yang, Yang Qiu, Meng Yu, Dechao Huang, Wei Zhou, Zongguang Wei, Yuquan Deng, Hongxin J Cell Mol Med Original Articles Long non‐coding RNAs (lncRNAs) have potential applications in clinical diagnosis and targeted cancer therapies. However, the expression profile of lncRNAs in colorectal cancer (CRC) initiation is still unclear. In this study, the expression profiles of lncRNAs and mRNAs were determined by microarray at specific tumour stages in an AOM/DSS‐induced primary colon cancer model. The temporal expression of lncRNAs was analysed by K‐means clustering. Additionally, weighted correlation network analysis (WGCNA) and gene ontology analysis were performed to construct co‐expression networks and establish functions of the identified lncRNAs and mRNAs. Our results suggested that 4307 lncRNAs and 5798 mRNAs are deregulated during CRC initiation. These differential expression genes (DEGs) exhibited a clear correlation with the differential stage of tumour initiation. WGCNA results suggested that a series of hub lncRNAs are involved in regulating cell stemness, colon inflammation, oxidative stress response and cell death at each stage. Among them, lncRNA H19 was up‐regulated in colon tumours and correlated with poor patient prognosis. Collectively, we have been the first to demonstrate the temporal expression and function of lncRNAs in CRC initiation. These results provide novel diagnosis and therapy targets for CRC. John Wiley and Sons Inc. 2019-03-28 2019-06 /pmc/articles/PMC6533480/ /pubmed/30920116 http://dx.doi.org/10.1111/jcmm.14300 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Dai, Lei
Li, Junshu
Dong, Zhexu
Liu, Yi
Chen, Ye
Chen, Na
Cheng, Lin
Fang, Chao
Wang, Huiling
Ji, Yanhong
Chen, Shuang
Su, Xiaolan
Shi, Gang
Lin, Yi
Zhang, Shuang
Yang, Yang
Qiu, Meng
Yu, Dechao
Huang, Wei
Zhou, Zongguang
Wei, Yuquan
Deng, Hongxin
Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation
title Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation
title_full Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation
title_fullStr Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation
title_full_unstemmed Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation
title_short Temporal expression and functional analysis of long non‐coding RNAs in colorectal cancer initiation
title_sort temporal expression and functional analysis of long non‐coding rnas in colorectal cancer initiation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533480/
https://www.ncbi.nlm.nih.gov/pubmed/30920116
http://dx.doi.org/10.1111/jcmm.14300
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