Suppr超能文献

子宫内膜癌中lncRNA的独特表达谱

Distinct expression profile of lncRNA in endometrial carcinoma.

作者信息

Xu Juan, Qian Yujia, Ye Min, Fu Ziyi, Jia Xuemei, Li Wenqu, Xu Pengfei, Lv Mingming, Huang Lei, Wang Luyu, Ruan Hongjie, Lv Juan

机构信息

Department of Obstetrics and Gynecology, Affiliated Obstetrics and Gynecology Hospital, Nanjing Medical University, Nanjing 210004, P.R. China.

Department of Breast Surgery, Affiliated Obstetrics and Gynecology Hospital, Nanjing Medical University, Nanjing 210004, P.R. China.

出版信息

Oncol Rep. 2016 Dec;36(6):3405-3412. doi: 10.3892/or.2016.5173. Epub 2016 Oct 14.

Abstract

Endometrial carcinoma (EC) is the most common malignancy in women. Dispite its prevalence, the prognosis of endometrial carcinoma still relies on conventional histological type, grade and invasion information. Its morbidity is still increasing and the outcome is very poor. To the best of our knowledge, hormonal imbalance and/or molecular genetic alterations are the main cause of EC. However, the alterations of lncRNAs which accounts for approximately 4/5 of human transcripts are still poorly understood. In the present study, using the RiboArray™ Custom Array, we studied the expression profiles of lncRNA in EC as compared to normal endometrium (NE) to find potential core lncRNAs for the diagnosis of EC. We found the potential core lncRNA by GO, KEGG, lncRNA and mRNA co-expression network. The potential functional lncRNAs were further detected by qPCR to validate the microarray results. A total of 172 lncRNAs and 188 mRNAs were found to be differentially expressed between type Ⅰ EC and the NE samples (fold change >1.5). qPCR validation showed good consistency with the microarray data. GO, pathway analysis, the lncRNA and mRNA co-expression network as well as the TCGA data revealed that 6 lncRNAs (KIAA0087, RP11-501O2, FAM212B-AS1, LOC102723552, RP11-140I24 and RP11-600K151) may be the core regulators of endometrial carcinogenesis. The potential core lncRNAs revealed by the mRNA and lncRNA co-expression network might be helpful to explore potential early diagnostic and therapeutic targets for EC.

摘要

子宫内膜癌(EC)是女性中最常见的恶性肿瘤。尽管其发病率很高,但子宫内膜癌的预后仍依赖于传统的组织学类型、分级和浸润信息。其发病率仍在上升,且预后很差。据我们所知,激素失衡和/或分子遗传改变是EC的主要病因。然而,占人类转录本约4/5的长链非编码RNA(lncRNA)的改变仍知之甚少。在本研究中,我们使用RiboArray™定制芯片,研究了EC与正常子宫内膜(NE)相比lncRNA的表达谱,以寻找用于EC诊断的潜在核心lncRNA。我们通过基因本体论(GO)、京都基因与基因组百科全书(KEGG)、lncRNA与mRNA共表达网络发现了潜在的核心lncRNA。通过定量聚合酶链反应(qPCR)进一步检测潜在的功能性lncRNA,以验证芯片结果。在Ⅰ型EC和NE样本之间共发现172个lncRNA和188个mRNA差异表达(倍数变化>1.5)。qPCR验证与芯片数据显示出良好的一致性。GO、通路分析、lncRNA与mRNA共表达网络以及癌症基因组图谱(TCGA)数据表明,6个lncRNA(KIAA0087、RP11-501O2、FAM212B-AS1、LOC102723552、RP11-140I24和RP11-600K151)可能是子宫内膜癌发生的核心调节因子。mRNA与lncRNA共表达网络揭示的潜在核心lncRNA可能有助于探索EC潜在的早期诊断和治疗靶点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验