The global expression profiling in esophageal squamous cell carcinoma

被引:29
作者
Dai Fuqiang [1 ]
Mei Longyong [1 ]
Meng Shenglan [1 ]
Ma Zheng [1 ]
Gao Wei [1 ]
Zhou Jinghai [1 ]
Zhang Jingge [1 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Inst Surg Res, Dept Thorac Surg, Chongqing, Peoples R China
关键词
Long no-coding RNAs; microRNAs; mRNAs; Expression profiling; Esophageal squamous cell carcinoma; GASTRIC-CANCER; INVASION; RNA; PROGRESSION; PROMOTES; PROLIFERATION; MIGRATION; MICRORNA; GROWTH; METASTASIS;
D O I
10.1016/j.ygeno.2017.04.005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Esophageal squamous cell carcinoma (ESCC) is the dominant subtype of esophageal cancer worldwide. This study aimed to explore the aberrant global expression profiling and construct regulatory network in ESCC for understanding tumorigenesis of ESCC. The expression pattern of long non-coding RNA (lncRNA), microRNA (miRNA) and mRNA was measured by RNA-sequencing in ESCC. Differentially expressed lncRNAs/miRNAs/mRNAs (DELs/DEMs/DEMIs) were identified in ESCC. DEMIs-DEMs network was constructed; hsa-miR-424-5p and hsa-miR-450b-5p were the hub miRNAs in the network, which negatively regulated 19 and 17 DEMs. DEMs targeted by DEMIs were significantly enriched in MAPK signaling pathway, pathways in cancer and focal adhesion signaling pathway. The expression of candidate DEMs and DEMIs in ESCC were validated through quantitative real-time polymerase chain reaction and microarray expression profiling analyses, and the results were generally consistent with our bioinformatics analysis. Our results might provide useful information for exploring the tumorigenesis mechanism and potentially therapeutic targets in ESCC. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:241 / 250
页数:10
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