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

J Cancer Res Ther. 2015 Apr-Jun;11(2):420-5. doi: 10.4103/0973-1482.160122.

Abstract

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.

MeSH terms

  • Arachidonic Acid / genetics
  • Carcinoma, Squamous Cell / genetics*
  • Cell Adhesion / genetics
  • Cell Differentiation / genetics
  • Cell Movement / genetics
  • Collagen / genetics
  • Computational Biology / methods
  • Databases, Genetic
  • Down-Regulation / genetics
  • Esophageal Neoplasms / genetics*
  • Esophageal Squamous Cell Carcinoma
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Neoplastic / genetics
  • Humans
  • Matrix Metalloproteinases / genetics
  • RNA / genetics*
  • Sequence Analysis, RNA / methods
  • Up-Regulation / genetics

Substances

  • Arachidonic Acid
  • RNA
  • Collagen
  • Matrix Metalloproteinases