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首页> 外文期刊>Journal of International Medical Research >Identification of key genes involved in the pathogenesis of cutaneous melanoma using bioinformatics analysis
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Identification of key genes involved in the pathogenesis of cutaneous melanoma using bioinformatics analysis

机译:使用生物信息分析鉴定涉及皮肤黑素瘤发病机制的关键基因

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Objective Malignant melanoma is a highly invasive cancer whose pathogenesis remains unclear. We analyzed the microarray dataset GDS1375 in the Gene Expression Omnibus database to search for key genes involved in the occurrence and development of melanoma. Methods The dataset included 52 samples (7 normal skin and 45 melanoma samples). We identified differentially expressed genes (DEGs) between the two groups and used integrated discovery databases for Gene Ontology (GO) and Kyoto Gene and Genome Encyclopedia (KEGG) pathway analyses. In addition, we used the STRING and MCODE plugins of Cytoscape to visualize the protein-protein interactions (PPI) for these DEGs. Results A total of 509 upregulated and 618 downregulated DEGs were identified, which were enriched in GO terms including integrin binding, protein binding, and structural constituent of cytoskeleton, and in KEGG pathways such as melanogenesis, prostate cancer, focal adhesion, and renin secretion. Three major modules from the PPI networks and 10 hub genes were identified, including CDC20 , GNB2 , PPP2R1A , AURKB , POLR2E , and AGTR1 . Overall survival was low when these six hub genes were highly expressed. Conclusion This bioinformatics analysis identified hub genes that may promote the development of melanoma and represent potential new biomarkers for diagnosis and treatment of melanoma.
机译:客观恶性黑色素瘤是一种高度侵入性的癌症,其发病机制仍然不清楚。我们在基因表达综合数据库中分析了微阵列数据集GDS1375,以寻找参与黑素瘤的发生和发展的关键基因。方法数据集包括52个样品(7个正常皮肤和45个黑色素瘤样品)。我们在两组之间鉴定了两组之间的差异表达基因(DEGS),并使用了基因本体(GO)和京都基因和基因组细胞基因(KEGG)途径分析的综合发现数据库。此外,我们使用Cytoscape的字符串和MCODE插件来可视化这些DEG的蛋白质 - 蛋白质相互作用(PPI)。结果总共509种上调和618个下调的次数,其富集,包括整合素结合,蛋白质结合和细胞骨架的结构组分,如糖核,前列腺癌,局灶性粘附和肾素分泌。鉴定了来自PPI网络和10个轮毂基因的三个主要模块,包括CDC20,GNB2,PPP2R1A,AurkB,PolR2e和Agtr1。当这六个轮毂基因高表达时,总存活率低。结论这种生物信息学分析鉴定了可能促进黑素瘤发展的轮毂基因,并代表潜在的新生物标志物进行黑素瘤的诊断和治疗。

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