RNA-sequencing based identification of crucial genes for esophageal squamous cell carcinoma

被引:5
|
作者
Fu, Jian-Hua
Wang, Li-Quan [1 ]
Li, Tao
Ma, Guo-Jun
机构
[1] Taishan Med Univ, Liaocheng Peoples Hosp, Dept Thorac Surg, Liaocheng, Shandong, Peoples R China
关键词
Esophageal squamous cell carcinoma; gene ontology analysis; KEGG pathway analysis; RNA-seq; RICH SECRETORY PROTEIN-3; LYMPH-NODE METASTASIS; DIFFERENTIAL EXPRESSION; PATHOLOGICAL STAGE; CANCER; OVEREXPRESSION; TISSUE; ASSOCIATION; PROGRESSION; MICROARRAY;
D O I
10.4103/0973-1482.160122
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: To identify key genes and pathways in the development of esophageal squamous cell carcinoma with RNA-seq data. Materials and Methods: RNA-seq data including three paired samples were downloaded from Sequence Read Archive database under accession number SRP007169 and differentially expressed genes (DEGs) were identified with package edge R of R. Functional enrichment analysis was performed to uncover their biological functions with the Database for Annotation, Visualization, and Integrated Discovery (DAVID) tools. Results: A total of 5561 DEGs were obtained, including 1829 upregulated and 3732 downregulated. Quite a few upregulated genes were components of collagen and matrix metallopeptidases (MMPs), which are involved in cell adhesion, cell mobility and so on. Keratin, mucin and cysteine-rich secretory protein were found to be significantly downregulated. Significantly over-represented biological processes for downregulated genes were epidermis development, epidermal cell differentiation and arachidonic acid metabolism. Conclusion: These identified DEGs may be underlying targets for diagnosis and treatment of esophageal squamous cell carcinoma.
引用
收藏
页码:420 / 425
页数:6
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