Wang Jiwen, Liu Han, Shen Xiaokun, Wang Yueqi, Zhang Dexiang, Shen Sheng, Suo Tao, Pan Hongtao, Ming Yue, Ding Kan, Liu Houbao
Department of General Surgery, Zhongshan Hospital, General Surgery Institute, Fudan University, Shanghai 200032, P.R. China.
Glycobiology and Glycochemistry Laboratory, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, P.R. China.
Oncol Lett. 2017 May;13(5):3508-3516. doi: 10.3892/ol.2017.5893. Epub 2017 Mar 22.
Gallbladder carcinoma (GBC) is the most common biliary tract cancer and exhibits poor patient prognosis. Previous studies have identified that long non-coding RNAs (lncRNAs) serve important regulatory roles in cancer biology. Alterations in lncRNAs are associated with several types of cancer. However, the contribution of lncRNAs to GBC remains unclear. To investigate the lncRNAs that are potentially involved in GBC, lncRNA profiles were identified in three pairs of human GBC and corresponding peri-carcinomatous tissue samples using microarray analysis. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to validate the microarray data. In order to elucidate potential functions, Gene Ontology, Kyoto Encyclopedia of Genes and Genomes analysis, and network analysis were used to determine relevant signaling pathways. Abundant RNA probes were used, and 1,758 lncRNAs and 1,254 mRNAs were detected to be differentially expressed by the microarray. Compared with para-carcinoma tissue, numerous lncRNAs were markedly upregulated or downregulated in GBC. The results demonstrated that the lncRNAs that were downregulated in GBC were more numerous compared with the lncRNAs that were upregulated. Among them, RP11-152P17.2-006 was the most upregulated, whereas CTA-941F9.9 was the most downregulated. The RT-qPCR results were consistent with the microarray data. Pathway analysis indicated that five pathways corresponded to the differentially expressed transcripts. It was demonstrated that lncRNA expression in GBC was markedly altered, and a series of novel lncRNAs associated with GBC were identified. The results of the present study suggest that the functions of lncRNAs are important in GBC development and progression.
胆囊癌(GBC)是最常见的胆道癌,患者预后较差。先前的研究已经确定,长链非编码RNA(lncRNA)在癌症生物学中发挥重要的调控作用。lncRNA的改变与多种类型的癌症相关。然而,lncRNA对GBC的作用仍不清楚。为了研究可能参与GBC的lncRNA,使用微阵列分析在三对人GBC及其相应的癌旁组织样本中鉴定了lncRNA谱。采用逆转录定量聚合酶链反应(RT-qPCR)验证微阵列数据。为了阐明潜在功能,使用基因本体论、京都基因与基因组百科全书分析和网络分析来确定相关信号通路。使用了大量RNA探针,微阵列检测到1758个lncRNA和1254个mRNA差异表达。与癌旁组织相比,GBC中有大量lncRNA明显上调或下调。结果表明,与上调的lncRNA相比,GBC中下调的lncRNA更多。其中,RP11-152P17.2-006上调最为明显,而CTA-941F9.9下调最为明显。RT-qPCR结果与微阵列数据一致。通路分析表明,五条通路与差异表达的转录本相对应。结果表明,GBC中lncRNA表达明显改变,并鉴定出一系列与GBC相关的新型lncRNA。本研究结果表明,lncRNA的功能在GBC的发生发展中具有重要作用。