Liu Qing, Wang Xinwen, Liu Yuan, Wei Minghui, Chen Lihua
State Key Laboratory of Military Stomatology, Department of Oral Medicine, School of Stomatology, Fourth Military Medical University, No. 145, Changle West Road, Xi'an, Shaanxi 710032, PR China.
State Key Laboratory of Military Stomatology, Department of Oral Medicine, School of Stomatology, Fourth Military Medical University, No. 145, Changle West Road, Xi'an, Shaanxi 710032, PR China.
Arch Oral Biol. 2016 Aug;68:61-5. doi: 10.1016/j.archoralbio.2016.03.018. Epub 2016 Mar 30.
Oral lichen planus (OLP) is a chronic inflammatory disease but aetiology and pathogenesis has not fully elucidated. To gain insight into the mechanism of OLP, bioinformatic analysis was performed in this study.
GSE38616 and GSE38615 were downloaded from GEO, including 7 cases of OLP and 7 healthy controls. Differentially expressed genes (DEGs) and miRNAs (DEMs) between OLP and control were screened with package Limma of R. Potential regulatory miRNAs were screened via gene set enrichment analysis. A protein-protein interaction network was constructed for the DEGs. KEGG pathways for DEGs were revealed using Gene Set Analysis Toolkit V2.
After DEGs and DEMs were obtained, potential regulatory miRNAs of the DEGs were revealed and only miR-362 was differentially expressed in OLP compared with DEMs. Four targets of miR-362 were SLIT-ROBO Rho GTPase activating protein 2 (SRGAP2), vesicle-associated membrane protein 4 (VAMP4), leucine rich repeat transmembrane neuronal 4 (LRRTM4) and lysine (K)-specific demethylase5C (KDM5C). Identified DEGs were significantly enriched in olfactory transduction and ribosome pathways.
miR-362, targeting SRGAP2 and VAMP4, may be a potential risk miRNA to regulate OLP. The findings may provide potential biomarkers for diagnosis or treatment of the disease.
口腔扁平苔藓(OLP)是一种慢性炎症性疾病,但其病因和发病机制尚未完全阐明。为深入了解OLP的发病机制,本研究进行了生物信息学分析。
从基因表达综合数据库(GEO)下载GSE38616和GSE38615数据集,包括7例OLP患者和7例健康对照。使用R语言的Limma软件包筛选OLP组和对照组之间的差异表达基因(DEGs)和微小RNA(DEMs)。通过基因集富集分析筛选潜在的调控微小RNA。构建DEGs的蛋白质-蛋白质相互作用网络。使用基因集分析工具包V2揭示DEGs的京都基因与基因组百科全书(KEGG)通路。
获得DEGs和DEMs后,揭示了DEGs的潜在调控微小RNA,与DEMs相比,仅miR-362在OLP中差异表达。miR-362的四个靶标是SLIT-ROBO Rho GTP酶激活蛋白2(SRGAP2)、囊泡相关膜蛋白4(VAMP4)、富含亮氨酸重复跨膜神经元蛋白4(LRRTM4)和赖氨酸(K)特异性去甲基化酶5C(KDM5C)。鉴定出的DEGs在嗅觉转导和核糖体通路中显著富集。
靶向SRGAP2和VAMP4的miR-362可能是调控OLP的潜在风险微小RNA。这些发现可能为该疾病的诊断或治疗提供潜在的生物标志物。