Expression profiles of long noncoding RNAs in cutaneous squamous cell carcinoma. (April 2016)

• Record Type: Journal Article
• Authors: Sand, Michael; Bechara, Falk G; Sand, Daniel; Gambichler, Thilo; Hahn, Stephan A; Bromba, Michael; Stockfleth, Eggert; Hessam, Schapoor
• Is Part Of: Epigenomics. Volume 8:Number 4(2016)
• Page Start: 501
• Page End: 518
• Publication Date: 2016-04
• Subjects: cutaneous squamous cell carcinoma -- epithelial skin cancer -- long noncoding RNAs -- noncoding RNAs -- nonmelanoma skin cancer; Epigenesis -- Periodicals; Genomics -- Periodicals; Chromatin -- Periodicals; DNA -- Periodicals; 572.87
• DOI: 10.2217/epi-2015-0012
• Languages: English
• ISSNs: 1750-1911

Abstract

Background: Despite there being over 35, 000 different long noncoding RNA (lncRNA) sequences described little is known regarding their molecular–pathological role in cutaneous squamous cell carcinoma (cSCC).Materials & methods: In this pilot study, lncRNA and mRNA expression profiles were determined in cSCC and control (n = 6) by an Arraystar human lncRNA Microarray. Kyoto Encyclopedia of Genes and Genomes pathway enrichment and gene ontology analysis of mRNAs was performed.Results: Analysis of differential expression revealed 1516 upregulated lncRNAs and 2586 downregulated lncRNAs in cSCC compared with controls. Data analysis identified known oncogenic lncRNAs, such as the HOX transcript antisense RNA HOTAIR, among the differentially expressed lncRNA sequences. Kyoto Encyclopedia of Genes and Genomes pathway analysis showed that focal adhesion, extracellular matrix and the oncogenic phosphatidylinositol 3′-kinase-Akt signaling pathway had the highest enrichment scores.Conclusion: This study provides the first evidence for differential expression of lncRNA in cSCC and serves as a template for further, larger functional in-depth analyses regarding cSCC molecular lncRNAs.