转录组
基因
结直肠癌
生物
癌症
鉴定(生物学)
基因表达
计算生物学
生物途径
癌症研究
生物信息学
遗传学
植物
作者
Xiaolin Hou,Nengyi Hou,Junwen Fu,Xuelai He,Haibo Xiong,Wei Xie,Guiqing Jia,Xiaofei Zuo,Xianpeng Qin,Minghui Pang
标识
DOI:10.1080/01635581.2020.1783328
摘要
Colorectal cancer (CRC) is the third most cancer-related death worldwide. This work aimed to identify potential hub genes and dysregulated pathways in the CRC by bioinformatics analysis. Three gene expression datasets were collected from GEO datasets, including tumor sample (N = 242) and adjacent nontumor tissue sample (N = 59). RankProd was used to discover the differential expressed genes between tumor and adjacent nontumor tissues for datasets generated by different laboratories. The gene set enrichment analysis conducted on the DE genes, followed by the protein–protein interaction (PPI) network. In total, 2,007 significant differential expression (DE) genes between tumor and adjacent nontumor tissues, include 1,090 upregulated genes and 917 downregulated genes in the tumor. The DE mRNAs are involved in cancer-related pathways. We comprehensively identified the CRC-related key mRNAs. Our data demonstrated combined different resources of transcriptomes will promote the understanding of the molecular mechanisms underlying CRC development and may be useful in discovering candidate molecular biomarkers for diagnosing, prognosis, and treating of CRC.
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