论文已发表
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IF 收录期刊
Authors Zhang X, Feng H, Li Z, Li D, Liu S, Huang H, Li M
Received 20 April 2018
Accepted for publication 11 July 2018
Published 19 September 2018 Volume 2018:11 Pages 6001—6021
DOI https://doi.org/10.2147/OTT.S171791
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Justinn Cochran
Peer reviewer comments 3
Editor who approved publication: Dr Carlos E Vigil
Purpose: Oral squamous cell carcinoma (OSCC) is one of the most common
malignant diseases worldwide, yet its molecular mechanisms are largely unknown.
We aimed to construct gene co-expression networks to identify key modules and
hub genes involved in the pathogenesis of OSCC.
Patients and
methods: We used dataset GSE30784 to
construct co-expression networks by weighted gene co-expression network
analysis (WGCNA). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and
Genomes (KEGG) enrichment analyses were performed by Database for Annotation,
Visualization and Integrated Discovery (DAVID). Hub genes were screened and
validated by other datasets.
Results: Turquoise and brown modules were found to be the most
significantly related to tumorigenesis. Functional enrichment analysis showed
that the turquoise module was associated with cell–cell adhesion, extracellular
matrix and collagen catabolic process. A total of 10 hub genes (MMP1 , TNFRSF12A , PLAU , FSCN1 , PDPN , KRT78 , EVPL , GGT6 , SMIM5 and CYSRT1 ) were identified and validated
at transcriptional and translational levels. Their genetic alteration and
survival analysis were also revealed.
Conclusion: We identified two modules and 10 hub genes, which were associated
with the tumorigenesis of OSCC. The two modules provided references that will
advance the understanding of mechanisms of tumorigenesis in OSCC. Moreover, the
hub genes may serve as biomarkers and therapeutic targets for precise diagnosis
and treatment of OSCC in the future.
Keywords: oral squamous cell carcinoma, co-expression, WGCNA, hub gene