Cheng Liyun, Shi Guijun, Fang Chunxiao, Li Guanghua, Zheng Yong, Chen Weigang
Department of Digestion, The First Affiliated Hospital, School of Medicine, Shihezi University, Shihezi, Xinjiang 832000, P.R. China.
Oncol Lett. 2019 Mar;17(3):2657-2668. doi: 10.3892/ol.2019.9904. Epub 2019 Jan 8.
Despite improvements in diagnosis and treatment, the survival of patients with advanced stages of esophageal squamous cell carcinoma (ESCC) remains poor. Therefore, novel biomarkers that can assist with early detection of ESCC are required. In the present study, three paired ESCC and normal esophageal tissue samples from Xinjiang Kazakh patients were obtained and microRNA (miRNA) microarray analysis was used to detect the differentially-expressed miRNAs. The target genes of the identified miRNAs were predicted using miRWalk software. A total of 23 miRNAs were differently expressed in Kazakh patients with ESCC. Gene Ontology enrichment analysis demonstrated that the upregulated miRNAs were predominantly associated with the 'vesicle' and 'membrane-bounded vesicle' terms, while the downregulated miRNAs were primarily associated with the term 'negative regulation of integrin-mediated signaling pathway'. The most highly enriched Kyoto Encyclopedia of Genes and Genomes pathway for the differentially-expressed miRNAs was 'Endocrine and other factor-regulated calcium reabsorption'. Protein-protein interaction network analysis revealed that IQ motif containing GTPase activating protein 1, RAB11A, lysine acetyltransferase 2B, catenin α 1 and tight junction protein 2 were hub genes of the network. In conclusion, a number of differentially-expressed miRNAs were identified in ESCC tissues samples from Xinjiang Kazakh patients, which may improve the understanding of the processes of tumorigenesis and development.
尽管在诊断和治疗方面有所改进,但晚期食管鳞状细胞癌(ESCC)患者的生存率仍然很低。因此,需要能够辅助早期检测ESCC的新型生物标志物。在本研究中,获取了来自新疆哈萨克族患者的三对ESCC和正常食管组织样本,并使用微小RNA(miRNA)微阵列分析来检测差异表达的miRNA。使用miRWalk软件预测已鉴定miRNA的靶基因。共有23种miRNA在哈萨克族ESCC患者中差异表达。基因本体富集分析表明,上调的miRNA主要与“囊泡”和“膜结合囊泡”术语相关,而下调的miRNA主要与“整合素介导的信号通路的负调控”术语相关。差异表达miRNA最富集的京都基因与基因组百科全书途径是“内分泌和其他因子调节的钙重吸收”。蛋白质-蛋白质相互作用网络分析显示,含IQ基序的GTP酶激活蛋白1、RAB11A、赖氨酸乙酰转移酶2B、连环蛋白α1和紧密连接蛋白2是该网络的枢纽基因。总之,在来自新疆哈萨克族患者的ESCC组织样本中鉴定出了一些差异表达的miRNA,这可能有助于增进对肿瘤发生和发展过程的理解。