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胰腺导管腺癌中的环状RNA表达

Circular RNA expression in pancreatic ductal adenocarcinoma.

作者信息

Zhang Qian, Wang Jin Yan, Zhou Si Ying, Yang Su Jin, Zhong Shan Liang

机构信息

Department of General Surgery, Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, Jiangsu 210009, P.R. China.

The First Clinical Medical College, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, P.R. China.

出版信息

Oncol Lett. 2019 Sep;18(3):2923-2930. doi: 10.3892/ol.2019.10624. Epub 2019 Jul 16.

Abstract

The regulatory roles of circular RNAs (circRNAs) in cancer are attracting increasing attention. The aim of the present study was to explore the roles of circRNAs in pancreatic ductal adenocarcinoma (PDAC) using microarray data. The circRNA and microRNA (miRNA) microarray data were downloaded from Gene Expression Omnibus. A total of 256 differentially expressed circRNAs were obtained by analyzing the circRNA microarray data from 26 pairs of PDAC and adjacent normal tissues. Differentially expressed miRNAs were analyzed using a dataset of 6 PDAC tissues and 5 non-neoplastic pancreas samples (GSE43796); 20 differentially expressed miRNAs were detected. circRNA/miRNA interactions were predicted between differentially expressed circRNAs and miRNAs using miRanda and RNAhybrid algorithms and 51 circRNA/miRNA interactions were obtained. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis using gene symbols of differentially expressed circRNAs demonstrated that 41 circRNAs were enriched in 17 pathways. Subnetworks that were associated with apoptosis or proliferation were extracted from the 17 pathways and a new network was constructed using Cytoscape software, which identified that mitogen-activated protein kinase, PI3K/AKT and WNT/β-catenin signaling pathways may be associated with PDAC development. In conclusion, 256 differentially expressed circRNAs and 20 differentially expressed miRNAs were identified in PDAC tissues compared with normal tissues; the circRNA/miRNA interactions and the networks of KEGG pathways provided a global view of the function of these differentially expressed circRNAs and miRNAs.

摘要

环状RNA(circRNAs)在癌症中的调控作用正受到越来越多的关注。本研究的目的是利用微阵列数据探索circRNAs在胰腺导管腺癌(PDAC)中的作用。circRNA和微小RNA(miRNA)微阵列数据从基因表达综合数据库下载。通过分析26对PDAC组织和相邻正常组织的circRNA微阵列数据,共获得256个差异表达的circRNAs。使用6个PDAC组织和5个非肿瘤胰腺样本的数据集(GSE43796)分析差异表达的miRNAs;检测到20个差异表达的miRNAs。使用miRanda和RNAhybrid算法预测差异表达的circRNAs和miRNAs之间的circRNA/miRNA相互作用,获得51个circRNA/miRNA相互作用。使用差异表达circRNAs的基因符号进行京都基因与基因组百科全书(KEGG)通路分析,结果表明41个circRNAs在17条通路中富集。从这17条通路中提取与凋亡或增殖相关的子网,并使用Cytoscape软件构建一个新的网络,该网络确定丝裂原活化蛋白激酶、PI3K/AKT和WNT/β-连环蛋白信号通路可能与PDAC的发生发展有关。总之,与正常组织相比,在PDAC组织中鉴定出256个差异表达的circRNAs和20个差异表达的miRNAs;circRNA/miRNA相互作用和KEGG通路网络提供了这些差异表达的circRNAs和miRNAs功能的全局视图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fc2/6676441/518a5cdc69be/ol-18-03-2923-g00.jpg

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