Tumor Etiology and Screening Department of Cancer Institute and General Surgery, the First Hospital of China Medical University, and Key Laboratory of Cancer Etiology and Prevention (China Medical University), Liaoning Provincial Education Department, 155# North Nanjing Street, Heping District, Shenyang City, 110001, Liaoning Province, China.
Dig Dis Sci. 2019 Jul;64(7):1868-1877. doi: 10.1007/s10620-019-05506-9. Epub 2019 Feb 7.
Competitive endogenous RNA (ceRNA) regulation suggested complex network of all transcript RNAs including long noncoding RNAs (lncRNAs), which can act as natural miRNA sponges to inhibit miRNA functions and modulate mRNA expression. Until now, the specific ceRNA regulatory mechanism of lncRNA-miRNA-mRNA in colorectal cancer (CRC) still remains unclear.
RNA sequencing data of 478 colon adenocarcinoma cases and 41 controls as well as 166 rectum adenocarcinoma cases and 10 controls were obtained from The Cancer Genome Atlas (TCGA) to investigate the significant changes of lncRNAs, miRNAs and mRNAs in colorectal carcinogenesis. The target lncRNAs and mRNAs of miRNAs were predicted by miRWalk. Functional and enrichment analyses were conducted by DAVID database. The lncRNA-miRNA-mRNA interaction network was constructed using Cytoscape.
We constructed ceRNA regulatory networks including 22 up-regulated lncRNAs, 12 down-regulated miRNAs and 122 up-regulated mRNAs, as well as 8 down-regulated lncRNAs, 43 up-regulated miRNAs and 139 down-regulated mRNAs. The GO enrichment showed that up-regulated genes mainly enriched in biological process including organic anion transport, collagen catabolic process, wound healing, Wnt receptor signalling and in pathways of tyrosine metabolism, taurine and hypotaurine metabolism, melanogenesis and phenylalanine metabolism. For down-regulated genes, significant enrichment was found in biological process of metal ion homeostasis, transmission of nerve impulse, cell-cell signalling, transmembrane transport and in pathways of ABC transporters, neuroactive ligand-receptor interaction, retinol metabolism, nitrogen metabolism and steroid hormone biosynthesis.
We identified significantly altered lncRNAs, miRNAs and mRNAs in colorectal carcinogenesis, which might serve as potential biomarkers for tumorigenesis of CRC. In addition, the ceRNA regulatory network of lncRNA-miRNA-mRNA was constructed, which would elucidate novel molecular mechanisms involved in initiation and progression of CRC, thus providing promising clues for clinical diagnosis and therapy.
竞争性内源 RNA(ceRNA)调节提示包括长链非编码 RNA(lncRNA)在内的所有转录 RNA 的复杂网络,lncRNA 可以作为天然 miRNA 海绵,抑制 miRNA 功能并调节 mRNA 表达。到目前为止,lncRNA-miRNA-mRNA 在结直肠癌(CRC)中的特定 ceRNA 调节机制仍不清楚。
从癌症基因组图谱(TCGA)获得了 478 例结肠腺癌病例和 41 例对照以及 166 例直肠腺癌病例和 10 例对照的 RNA 测序数据,以研究结直肠发生过程中 lncRNA、miRNA 和 mRNA 的显著变化。通过 miRWalk 预测 miRNA 的靶 lncRNA 和 mRNA。使用 DAVID 数据库进行功能和富集分析。使用 Cytoscape 构建 lncRNA-miRNA-mRNA 相互作用网络。
我们构建了 ceRNA 调控网络,包括 22 个上调的 lncRNA、12 个下调的 miRNA 和 122 个上调的 mRNA,以及 8 个下调的 lncRNA、43 个上调的 miRNA 和 139 个下调的 mRNA。GO 富集表明上调基因主要富集在生物过程中,包括有机阴离子转运、胶原分解代谢、伤口愈合、Wnt 受体信号转导以及酪氨酸代谢、牛磺酸和次牛磺酸代谢、黑色素生成和苯丙氨酸代谢途径。对于下调基因,在生物过程中发现了显著的富集,包括金属离子稳态、神经冲动传递、细胞间信号转导、跨膜转运以及 ABC 转运蛋白、神经活性配体-受体相互作用、视黄醇代谢、氮代谢和甾体激素生物合成途径。
我们鉴定了结直肠癌发生过程中显著改变的 lncRNA、miRNA 和 mRNA,它们可能作为 CRC 肿瘤发生的潜在生物标志物。此外,构建了 lncRNA-miRNA-mRNA 的 ceRNA 调控网络,这将阐明 CRC 起始和进展中涉及的新分子机制,从而为临床诊断和治疗提供有希望的线索。