State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center for Biotherapy, Chengdu, P. R. China.
Department of Medical Oncology, Cancer Center, the State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu, P. R. China.
J Cell Mol Med. 2019 Jun;23(6):4127-4138. doi: 10.1111/jcmm.14300. Epub 2019 Mar 28.
Long non-coding RNAs (lncRNAs) have potential applications in clinical diagnosis and targeted cancer therapies. However, the expression profile of lncRNAs in colorectal cancer (CRC) initiation is still unclear. In this study, the expression profiles of lncRNAs and mRNAs were determined by microarray at specific tumour stages in an AOM/DSS-induced primary colon cancer model. The temporal expression of lncRNAs was analysed by K-means clustering. Additionally, weighted correlation network analysis (WGCNA) and gene ontology analysis were performed to construct co-expression networks and establish functions of the identified lncRNAs and mRNAs. Our results suggested that 4307 lncRNAs and 5798 mRNAs are deregulated during CRC initiation. These differential expression genes (DEGs) exhibited a clear correlation with the differential stage of tumour initiation. WGCNA results suggested that a series of hub lncRNAs are involved in regulating cell stemness, colon inflammation, oxidative stress response and cell death at each stage. Among them, lncRNA H19 was up-regulated in colon tumours and correlated with poor patient prognosis. Collectively, we have been the first to demonstrate the temporal expression and function of lncRNAs in CRC initiation. These results provide novel diagnosis and therapy targets for CRC.
长链非编码 RNA(lncRNAs)在临床诊断和靶向癌症治疗中有潜在的应用。然而,lncRNAs 在结直肠癌(CRC)起始中的表达谱尚不清楚。在这项研究中,通过微阵列在 AOM/DSS 诱导的原发性结肠癌模型中的特定肿瘤阶段确定了 lncRNAs 和 mRNAs 的表达谱。通过 K-means 聚类分析 lncRNAs 的时间表达。此外,进行了加权相关网络分析(WGCNA)和基因本体分析,以构建共表达网络,并确定鉴定的 lncRNAs 和 mRNAs 的功能。我们的结果表明,在 CRC 起始过程中,有 4307 个 lncRNAs 和 5798 个 mRNAs 被下调。这些差异表达基因(DEGs)与肿瘤起始的不同阶段具有明显的相关性。WGCNA 结果表明,一系列枢纽 lncRNAs 参与调节每个阶段的细胞干性、结肠炎症、氧化应激反应和细胞死亡。其中,lncRNA H19 在结肠肿瘤中上调,并与患者预后不良相关。总之,我们首次证明了 lncRNAs 在 CRC 起始中的时间表达和功能。这些结果为 CRC 提供了新的诊断和治疗靶点。