Genome-wide gene expression profiling of tongue squamous cell carcinoma by RNA-seq
Autor: | Chao Deng, Ousheng Liu, Haixia Zhang, Chun Hong Hu, Yan He, Jin An Ma, Zhan Gui Tang, Ye Qian Feng |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Down-Regulation Genome-wide association study RNA-Seq Real-Time Polymerase Chain Reaction 03 medical and health sciences 0302 clinical medicine HMGA2 Gene expression Humans General Dentistry Gene Epithelial cell differentiation biology Sequence Analysis RNA Gene Expression Profiling Molecular biology Tongue Neoplasms Up-Regulation Gene expression profiling 030104 developmental biology Real-time polymerase chain reaction 030220 oncology & carcinogenesis Carcinoma Squamous Cell biology.protein Genome-Wide Association Study |
Zdroj: | Clinical Oral Investigations. 22:209-216 |
ISSN: | 1436-3771 1432-6981 |
DOI: | 10.1007/s00784-017-2101-7 |
Popis: | Tongue squamous cell carcinoma (TSCC) is significantly more malignant than other type of oral squamous cell carcinoma (OSCC). In this study, we aimed to identify specific global gene expression signatures of TSCC to investigate the more invasive behavior of the deeply infiltrating cancer. Using RNA-seq technology, we detected gene expression of 20 TSCCs, 20 matched paratumor tissues, and 10 healthy normal mucosa tissues. Enrichment analysis of gene ontology (GO) and pathway was conducted using online tools DAVID for the dysregulated genes. Additionally, we performed the quantitative real-time RT-PCR (qRT-PCR) to validate the findings of RNA-Seq in 10 samples of TSCC, matched paratumor, and normal mucosa, respectively. We detected 252 differentially expressed genes (DEGs) between TSCC and matched paratumor tissue, including 117 up-regulated and 135 down-regulated genes. For comparison between TSCC and normal mucosa, 234 DEGS were identified, consisting of 67 up-regulated and 167 down-regulated genes. For both two comparisons, GO categories of muscle contraction (GO: 0006936), epidermis development (GO: 0008544), epithelial cell differentiation (GO: 0030855), and keratinization (GO: 0031424) were commonly enriched. Altered gene expression affected some cancer-related pathways, such as tight junction. The qRT-PCR validation showed that gene expression patterns of FOLR1, NKX3-1, TFF3, PIGR, NEFL, MMP13, and HMGA2 were fully in concordance with RNA-Seq results. Findings in this study demonstrated the genetic and molecular alterations associated with TSCC, providing new clues for understanding the molecular mechanisms of TSCC pathogenesis. |
Databáze: | OpenAIRE |
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