首页> 外文期刊>Annals of Dermatology >Gene Expression Patterns of Cutaneous Squamous Cell Carcinoma and Actinic Keratosis: Biomarkers Screening for Skin Disease Diagnosis
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Gene Expression Patterns of Cutaneous Squamous Cell Carcinoma and Actinic Keratosis: Biomarkers Screening for Skin Disease Diagnosis

机译:皮肤鳞状细胞癌和光化性角化病的基因表达模式:皮肤疾病诊断的生物标志物筛选

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Background pActinic keratosis (AK) was an intraepidermal tumor which caused by ultraviolet irradiation-induced skin damage. Objective pThe aim was to screen biomarkers for development of skin disease by comparing the gene expression profiles between cutaneous squamous cell carcinoma (CSCC) and AK. Methods pGSE45216 with 30 cutaneous squamous cell carcinoma patients and 10 actinic keratosis patients were downloaded and significance analysis of microarrays was processed to screen differently expressed genes (DEGs). Fisher's exact test was processed for DEGs enrichment. Pathway relationship network systematically reflected the signal conduction and synergism between enriched pathways based on Kyoto Encyclopedia of Genes and Genomes database. Gene co-expression network was constructed according to gene expression data. Quantitative real-time-PCR was used to verify screened biomarkers. Results pTotal 410 DEGs were screened and enriched into various functions, such as signal transduction and negative regulation of apoptotic process. They also participated into cytokine-cytokine receptor interaction and focal adhesion. The pathway relationship network was constructed with 27 nodes. Hub nodes with higher degree of this network were mitogen-activated protein kinase signaling pathway and apoptosis. The gene co-expression network was constructed with 39 nodes. Thereinto, hub node was ELOVL fatty acid elongase. The expression levels of ELOVL4 and HPGD were significantly higher in CSCC samples than that in AK samples, while the expression levels of INHBA and LAMC2 in CSCC samples were significantly lower than that in AK samples. Conclusion pThese screened genes, including ELOVL4, HPGD, INHBA and LAMC2, played important roles in transformation from AK to CSCC.
机译:背景技术光化性角化病(AK)是一种表皮内肿瘤,由紫外线照射引起的皮肤损伤引起。目的>目的是通过比较皮肤鳞状细胞癌(CSCC)和AK之间的基因表达谱来筛选皮肤疾病发展的生物标志物。方法下载30例皮肤鳞状细胞癌患者和10例光化性角化病患者的> GSE45216,并进行微阵列显着性分析以筛选差异表达基因(DEG)。 Fisher的精确测试用于DEG富集。通路关系网络基于《京都议定书》和基因组数据库,系统地反映了丰富通路之间的信号传导和协同作用。根据基因表达数据构建基因共表达网络。实时定量PCR用于验证筛选的生物标志物。结果总共筛选了410个DEG,并将其富集到各种功能中,例如信号转导和凋亡过程的负调控。他们还参与了细胞因子-细胞因子受体的相互作用和粘着斑。路径关系网络由27个节点构成。具有较高程度该网络的枢纽节点是有丝分裂原激活的蛋白激酶信号传导途径和细胞凋亡。基因共表达网络由39个节点组成。其中,枢纽节点是ELOVL脂肪酸延长酶。 CSCC样品中ELOVL4和HPGD的表达水平显着高于AK样品,而CSH样品中INHBA和LAMC2的表达水平显着低于AK样品。结论>这些筛选的基因,包括ELOVL4,HPGD,INHBA和LAMC2,在从AK到CSCC的转化中发挥了重要作用。

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