Center for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054, China.
School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 610054, China.
Int J Biol Sci. 2018 May 22;14(8):833-842. doi: 10.7150/ijbs.24816. eCollection 2018.
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. 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. 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. 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.
基于之前明确定义的三种胃腺癌亚型(浸润型、增殖型和代谢型),我们旨在寻找每种亚型的潜在生物标志物和生物学特征。首先构建了每种胃癌亚型的全基因组共表达网络,然后对每个全基因组共表达网络中的功能模块进行划分,接着从每个功能模块中筛选关键基因,最后对关键基因进行富集分析,挖掘每种亚型的生物学特征。对每对亚型进行比较分析,以发现不同亚型之间的共同和独特特征。在浸润型中鉴定出 207 个关键基因,在增殖型中鉴定出 215 个关键基因,在代谢型中鉴定出 204 个关键基因。与现有相关研究相比,每个亚型中的大多数关键基因都是独特的新发现。对每个亚型关键基因的 GO 和 KEGG 富集分析揭示了每个亚型的重要生物学特征。对于一个亚型,大多数鉴定出的关键基因和重要的生物学特征都是独特的,这意味着关键基因可以作为亚型的潜在生物标志物,并且胃腺癌的每种亚型可能具有不同的发生和发展机制。因此,应该对浸润型、增殖型和代谢型胃腺癌采用不同的诊断和治疗方法。