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Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma

Pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive and lethal malignancies. Long non-coding RNAs (lncRNAs) are a novel class of non-protein-coding transcripts that have been implicated in cancer biogenesis and prognosis. By repurposing microarray probes, we herein analysed th...

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Autores principales: Fu, Xue-Liang, Liu, De-Jun, Yan, Ting-Ting, Yang, Jian-Yu, Yang, Min-Wei, Li, Jiao, Huo, Yan-Miao, Liu, Wei, Zhang, Jun-Feng, Hong, Jie, Hua, Rong, Chen, Hao-Yan, Sun, Yong-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024322/
https://www.ncbi.nlm.nih.gov/pubmed/27628540
http://dx.doi.org/10.1038/srep33535
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author Fu, Xue-Liang
Liu, De-Jun
Yan, Ting-Ting
Yang, Jian-Yu
Yang, Min-Wei
Li, Jiao
Huo, Yan-Miao
Liu, Wei
Zhang, Jun-Feng
Hong, Jie
Hua, Rong
Chen, Hao-Yan
Sun, Yong-Wei
author_facet Fu, Xue-Liang
Liu, De-Jun
Yan, Ting-Ting
Yang, Jian-Yu
Yang, Min-Wei
Li, Jiao
Huo, Yan-Miao
Liu, Wei
Zhang, Jun-Feng
Hong, Jie
Hua, Rong
Chen, Hao-Yan
Sun, Yong-Wei
author_sort Fu, Xue-Liang
collection PubMed
description Pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive and lethal malignancies. Long non-coding RNAs (lncRNAs) are a novel class of non-protein-coding transcripts that have been implicated in cancer biogenesis and prognosis. By repurposing microarray probes, we herein analysed the lncRNA expression profiles in two public PDAC microarray datasets and identified 34 dysregulated lncRNAs in PDAC. In addition, the expression of 6 selected lncRNAs was confirmed in Ren Ji cohort and pancreatic cell lines, and their association with 80 PDAC patients’ clinicopathological features and prognosis was investigated. Results indicated that AFAP1-AS1, UCA1 and ENSG00000218510 might be involved in PDAC progression and significantly associated with overall survival of PDAC. UCA1 and ENSG00000218510 expression status may serve as independent prognostic biomarkers for overall survival of PDAC. Gene set enrichment analysis (GSEA) analysis suggested that high AFAP1-AS1, UCA1 and low ENSG00000218510 expression were correlated with several tumorigenesis related pathways. Functional experiments demonstrated that AFAP1-AS1 and UCA1 were required for efficient invasion and/or proliferation promotion in PDAC cell lines, while ENSG00000218510 acted the opposite. Our findings provide novel information on lncRNAs expression profiles which might be beneficial to the precise diagnosis, subcategorization and ultimately, the individualized therapy of PDAC.
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spelling pubmed-50243222016-09-20 Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma Fu, Xue-Liang Liu, De-Jun Yan, Ting-Ting Yang, Jian-Yu Yang, Min-Wei Li, Jiao Huo, Yan-Miao Liu, Wei Zhang, Jun-Feng Hong, Jie Hua, Rong Chen, Hao-Yan Sun, Yong-Wei Sci Rep Article Pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive and lethal malignancies. Long non-coding RNAs (lncRNAs) are a novel class of non-protein-coding transcripts that have been implicated in cancer biogenesis and prognosis. By repurposing microarray probes, we herein analysed the lncRNA expression profiles in two public PDAC microarray datasets and identified 34 dysregulated lncRNAs in PDAC. In addition, the expression of 6 selected lncRNAs was confirmed in Ren Ji cohort and pancreatic cell lines, and their association with 80 PDAC patients’ clinicopathological features and prognosis was investigated. Results indicated that AFAP1-AS1, UCA1 and ENSG00000218510 might be involved in PDAC progression and significantly associated with overall survival of PDAC. UCA1 and ENSG00000218510 expression status may serve as independent prognostic biomarkers for overall survival of PDAC. Gene set enrichment analysis (GSEA) analysis suggested that high AFAP1-AS1, UCA1 and low ENSG00000218510 expression were correlated with several tumorigenesis related pathways. Functional experiments demonstrated that AFAP1-AS1 and UCA1 were required for efficient invasion and/or proliferation promotion in PDAC cell lines, while ENSG00000218510 acted the opposite. Our findings provide novel information on lncRNAs expression profiles which might be beneficial to the precise diagnosis, subcategorization and ultimately, the individualized therapy of PDAC. Nature Publishing Group 2016-09-15 /pmc/articles/PMC5024322/ /pubmed/27628540 http://dx.doi.org/10.1038/srep33535 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ 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 Article
Fu, Xue-Liang
Liu, De-Jun
Yan, Ting-Ting
Yang, Jian-Yu
Yang, Min-Wei
Li, Jiao
Huo, Yan-Miao
Liu, Wei
Zhang, Jun-Feng
Hong, Jie
Hua, Rong
Chen, Hao-Yan
Sun, Yong-Wei
Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma
title Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma
title_full Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma
title_fullStr Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma
title_full_unstemmed Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma
title_short Analysis of long non-coding RNA expression profiles in pancreatic ductal adenocarcinoma
title_sort analysis of long non-coding rna expression profiles in pancreatic ductal adenocarcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5024322/
https://www.ncbi.nlm.nih.gov/pubmed/27628540
http://dx.doi.org/10.1038/srep33535
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