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Genome-wide Analyses on Single Disease Samples for Potential Biomarkers and Biological Features of Molecular Subtypes: A Case Study in Gastric Cancer

机译:全基因组分析潜在疾病标志物和分子亚型的生物学特征的单一疾病样品:胃癌的案例研究。

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摘要

>Purpose: Based on the previous 3 well-defined subtypes of gastric adenocarcinoma (invasive, proliferative and metabolic), we aimed to find potential biomarkers and biological features of each subtype.>Methods: The genome-wide co-expression network of each subtype of gastric cancer was firstly constructed. Then, the functional modules in each genome-wide co-expression network were divided. Next, the key genes were screened from each functional module. Finally, the enrichment analysis was performed on the key genes to mine the biological features of each subtype. Comparative analysis between each pair of subtypes was performed to find the common and unique features among different subtypes.>Results: A total of 207 key genes were identified in invasive, 215 key genes in proliferative, and 204 key genes in metabolic subtypes. Most key genes in each subtype were unique and new findings compared with that of the existing related researches. The GO and KEGG enrichment analyses for the key genes of each subtype revealed important biological features of each subtype.>Conclusions: For a subtype, most identified key genes and important biological features were unique, which means that the key genes can be used as the potential biomarker of a subtype, and each subtype of gastric cancer might have different occurrence and development mechanisms. Thus, different diagnosis and therapy methods should be applied to the invasive, proliferative and metabolic subtypes of gastric cancer.
机译:>目的:基于胃腺癌的前3种明确定义的亚型(侵袭性,增生性和代谢性),我们旨在寻找每种亚型的潜在生物标志物和生物学特征。>方法:首先建立了每种胃癌亚型的全基因组共表达网络。然后,每个基因组范围内的共表达网络中的功能模块被划分。接下来,从每个功能模块中筛选关键基因。最后,对关键基因进行了富集分析,以挖掘每种亚型的生物学特征。进行每对亚型之间的比较分析,以发现不同亚型之间的共性和独特性。>结果:入侵性中共鉴定出207个关键基因,增殖中鉴定了215个关键基因,204个关键基因在代谢亚型中。与现有的相关研究相比,每种亚型中的大多数关键基因都是独特的且具有新发现。对每个亚型的关键基因进行GO和KEGG富集分析,揭示了每个亚型的重要生物学特征。>结论:对于一个亚型,大多数鉴定出的关键基因和重要生物学特征是唯一的,这意味着关键基因可以用作一种亚型的潜在生物标志物,每种胃癌亚型可能具有不同的发生和发展机制。因此,应将不同的诊断和治疗方法应用于胃癌的浸润,增生和代谢亚型。

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