Construction and analysis of dysregulated lncRNA‐associated ceRNA network in colorectal cancer

Colorectal cancer (CRC) is one of the most frequently diagnosed digestive system cancer. The aim of the present study was to investigate the interactions among messenger RNAs (mRNAs), microRNAs (miRNAs), and long noncoding RNAs (lncRNAs) in CRC to reveal the mechanisms of CRC. Differentially expressed genes (DEGs) were identified from public gene expression data sets. One thousand eighty‐one common dysregulated mRNAs in two data sets were identified. Gene function analysis and protein‐protein interaction network analysis indicated that these DEGs might play important roles in CRC. LINC00365 was selected through coding‐ noncoding network analysis and its expression was validated upregulated in 22 paired clinical samples and four CRC cell lines. A competing endogenous RNA network composed of 70 miRNAs, nine mRNAs, and LINC00365 was constructed. Eight of nine mRNAs were validated upregulated in The Cancer Genome Atlas data set. Our results suggested that LINC00365 was an oncogene in CRC and it could regulate the expression of several mRNAs through sponging miRNAs. Through bioinformatics analysis and validation in The Cancer Genome Atlas data set, this study suggested that LINC00365 was a potential oncogene in CRC. The expression of LINC00365 was validated upregulated in CRC cell lines and clinical samples and the result of bioinformatics analysis indicated that it could regulate several messenger RNAs through sponging microRNAs