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Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells

Preoperative 5-fluorouracil- (5-FU-) based chemoradiotherapy is a standard treatment for locally advanced colorectal cancer (CRC). However, the effect of 5-FU-based chemoradiotherapy on CRC is limited due to the development of chemoradiation resistance (CRR), and the molecular mechanisms underlying...

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Autores principales: Xiong, Wei, Ai, Yi-Qin, Li, Yun-Fen, Ye, Qing, Chen, Zheng-Ting, Qin, Ji-Yong, Liu, Qiu-Yan, Wang, Hong, Ju, Yun-He, Li, Wen-Hui, Li, Yun-Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471554/
https://www.ncbi.nlm.nih.gov/pubmed/28656150
http://dx.doi.org/10.1155/2017/8421614
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author Xiong, Wei
Ai, Yi-Qin
Li, Yun-Fen
Ye, Qing
Chen, Zheng-Ting
Qin, Ji-Yong
Liu, Qiu-Yan
Wang, Hong
Ju, Yun-He
Li, Wen-Hui
Li, Yun-Feng
author_facet Xiong, Wei
Ai, Yi-Qin
Li, Yun-Fen
Ye, Qing
Chen, Zheng-Ting
Qin, Ji-Yong
Liu, Qiu-Yan
Wang, Hong
Ju, Yun-He
Li, Wen-Hui
Li, Yun-Feng
author_sort Xiong, Wei
collection PubMed
description Preoperative 5-fluorouracil- (5-FU-) based chemoradiotherapy is a standard treatment for locally advanced colorectal cancer (CRC). However, the effect of 5-FU-based chemoradiotherapy on CRC is limited due to the development of chemoradiation resistance (CRR), and the molecular mechanisms underlying this resistance are yet to be investigated. Recently, circular RNAs (circRNAs), which can function as microRNA sponges, were found to be involved in the development of several cancers. In this study, we focused on clarifying the modulation of the expression profiles of circRNAs in CRR. Microarray analysis identified 71 circRNAs differentially expressed in chemoradiation-resistant CRC cells. Among them, 47 were upregulated and 24 were downregulated by more than twofold. Furthermore, expression modulation of five representative circRNAs was validated by quantitative reverse transcription PCR (qRT-PCR). Moreover, these modulated circRNAs were predicted to interact with 355 miRNAs. Furthermore, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that the most modulated circRNAs regulate several cancers and cancer-related pathways, and the possible mechanism underlying CRR was discussed. This is the first report revealing the circRNA modulations in 5-FU chemoradiation-resistant CRC cells by microarray. The study provided a useful database for further understanding CRR and presents potential targets to overcome CRR in CRC.
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spelling pubmed-54715542017-06-27 Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells Xiong, Wei Ai, Yi-Qin Li, Yun-Fen Ye, Qing Chen, Zheng-Ting Qin, Ji-Yong Liu, Qiu-Yan Wang, Hong Ju, Yun-He Li, Wen-Hui Li, Yun-Feng Biomed Res Int Research Article Preoperative 5-fluorouracil- (5-FU-) based chemoradiotherapy is a standard treatment for locally advanced colorectal cancer (CRC). However, the effect of 5-FU-based chemoradiotherapy on CRC is limited due to the development of chemoradiation resistance (CRR), and the molecular mechanisms underlying this resistance are yet to be investigated. Recently, circular RNAs (circRNAs), which can function as microRNA sponges, were found to be involved in the development of several cancers. In this study, we focused on clarifying the modulation of the expression profiles of circRNAs in CRR. Microarray analysis identified 71 circRNAs differentially expressed in chemoradiation-resistant CRC cells. Among them, 47 were upregulated and 24 were downregulated by more than twofold. Furthermore, expression modulation of five representative circRNAs was validated by quantitative reverse transcription PCR (qRT-PCR). Moreover, these modulated circRNAs were predicted to interact with 355 miRNAs. Furthermore, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis showed that the most modulated circRNAs regulate several cancers and cancer-related pathways, and the possible mechanism underlying CRR was discussed. This is the first report revealing the circRNA modulations in 5-FU chemoradiation-resistant CRC cells by microarray. The study provided a useful database for further understanding CRR and presents potential targets to overcome CRR in CRC. Hindawi 2017 2017-06-01 /pmc/articles/PMC5471554/ /pubmed/28656150 http://dx.doi.org/10.1155/2017/8421614 Text en Copyright © 2017 Wei Xiong et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Xiong, Wei
Ai, Yi-Qin
Li, Yun-Fen
Ye, Qing
Chen, Zheng-Ting
Qin, Ji-Yong
Liu, Qiu-Yan
Wang, Hong
Ju, Yun-He
Li, Wen-Hui
Li, Yun-Feng
Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells
title Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells
title_full Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells
title_fullStr Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells
title_full_unstemmed Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells
title_short Microarray Analysis of Circular RNA Expression Profile Associated with 5-Fluorouracil-Based Chemoradiation Resistance in Colorectal Cancer Cells
title_sort microarray analysis of circular rna expression profile associated with 5-fluorouracil-based chemoradiation resistance in colorectal cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5471554/
https://www.ncbi.nlm.nih.gov/pubmed/28656150
http://dx.doi.org/10.1155/2017/8421614
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