Suppr超能文献

基于转录组测序和生物信息学分析鉴定胃癌差异表达的长链非编码 RNA。

Identification of differential expression lncRNAs in gastric cancer using transcriptome sequencing and bioinformatics analyses.

机构信息

Department of Laboratory Medicine, Shanghai Shuguang Hospital Affiliated with Shanghai University of TCM, Shanghai 200021, P.R. China.

出版信息

Mol Med Rep. 2018 Jun;17(6):8189-8195. doi: 10.3892/mmr.2018.8889. Epub 2018 Apr 16.

Abstract

The current study aimed to identify novel long non‑coding RNAs (lncRNAs) associated with gastric cancer (GC). Transcriptome sequencing of the lncRNAs and mRNAs from GC tissues and normal adjacent tissues was performed. The data were analyzed using bioinformatics analysis, specifically analysis of differentially expressed lncRNAs and mRNA, target gene prediction and functional enrichment analysis. A total of 1,181 differentially expressed mRNA and 390 differentially expressed lncRNAs were identified. The targets of upregulated lncRNAs were significantly enriched in functions associated with collagen fibril organization, whereas the downregulated lncRNA were significantly associated with ion transmembrane transport and regulation of membrane potential. A total of 7 lncRNAs were verified by reverse transcription‑quantitative polymerase chain reaction (RT‑qPCR). Following RT‑qPCR validation, AC016735.2, AP001626.1, RP11‑400N13.3 and RP11‑243M5.2 were considered to be consistent with the prediction of the bioinformatics analysis. Transcriptome sequencing and RT‑qPCR experiments identified 4 lncRNAs, including AC016735.2, AP001626.1, RP11‑400N13.3 and RP11‑243M5.2 to have an important role in the carcinogenesis of GC.

摘要

本研究旨在鉴定与胃癌(GC)相关的新型长链非编码 RNA(lncRNA)。对 GC 组织和正常相邻组织的 lncRNA 和 mRNA 进行转录组测序。使用生物信息学分析对数据进行分析,特别是差异表达的 lncRNA 和 mRNA、靶基因预测和功能富集分析。鉴定出 1181 个差异表达的 mRNA 和 390 个差异表达的 lncRNA。上调 lncRNA 的靶基因显著富集在与胶原纤维组织相关的功能中,而下调的 lncRNA 则与离子跨膜转运和膜电位调节显著相关。通过逆转录-定量聚合酶链反应(RT-qPCR)验证了 7 个 lncRNA。经过 RT-qPCR 验证,AC016735.2、AP001626.1、RP11-400N13.3 和 RP11-243M5.2 被认为与生物信息学分析的预测一致。转录组测序和 RT-qPCR 实验鉴定出 4 个 lncRNA,包括 AC016735.2、AP001626.1、RP11-400N13.3 和 RP11-243M5.2,它们在 GC 的致癌作用中具有重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验