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Differential co-expression analysis of a microarray gene expression profiles of pulmonary adenocarcinoma

机译:肺腺癌微阵列基因表达谱的差异共表达分析

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Lung cancer severely reduces the quality of life worldwide and causes high socioeconomic burdens. However, key genes leading to the generation of pulmonary adenocarcinoma remain elusive despite intensive research efforts. The present study aimed to identify the potential associations between transcription factors (TFs) and differentially co-expressed genes (DCGs) in the regulation of transcription in pulmonary adenocarcinoma. Gene expression profiles of pulmonary adenocarcinoma were downloaded from the Gene Expression Omnibus, and gene expression was analyzed using a computational method. A total of 37,094 differentially co-expressed links (DCLs) and 251 DCGs were identified, which were significantly enriched in 10 pathways. The construction of the regulatory network and the analysis of the regulatory impact factors revealed eight crucial TFs in the regulatory network. These TFs regulated the expression of DCGs by promoting or inhibiting their expression. In addition, certain TFs and target genes associated with DCGs did not appear in the DCLs, which indicated that those TFs could be synergistic with other factors. This is likely to provide novel insights for research into pulmonary adenocarcinoma. In conclusion, the present study may enhance the understanding of disease mechanisms and lead to an improved diagnosis of lung cancer. However, further studies are required to confirm these observations.
机译:肺癌严重降低了全世界的生活质量,并造成了很高的社会经济负担。但是,尽管进行了深入的研究,导致肺腺癌发生的关键基因仍然难以捉摸。本研究旨在确定肺腺癌转录调控中转录因子(TFs)和差异共表达基因(DCGs)之间的潜在关联。从Gene Expression Omnibus下载了肺腺癌的基因表达谱,并使用计算方法分析了基因表达。共鉴定到37,094个差异共表达链接(DCL)和251个DCG,它们在10条途径中显着富集。监管网络的建设以及对监管影响因素的分析揭示了监管网络中的八个关键TF。这些TF通过促进或抑制DCG的表达来调节其表达。此外,某些DCs中与DCGs相关的TFs和靶基因未出现,这表明这些TFs可能与其他因素具有协同作用。这可能为肺腺癌的研究提供新颖的见解。总而言之,本研究可能会增强对疾病机制的了解,并改善肺癌的诊断。但是,需要进一步的研究来确认这些观察结果。

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