Duan Weicheng, Wang Kang, Duan Yijie, Chen Xiuyi, Chu Xufeng, Hu Ping, Xiong Bo
Department of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Key Laboratory of Environment and Health (HUST), Ministry of Education, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Front Oncol. 2021 Apr 23;11:615234. doi: 10.3389/fonc.2021.615234. eCollection 2021.
Malignant pleural mesothelioma (MPM) is a highly aggressive cancer with short survival time. Unbalanced competing endogenous RNAs (ceRNAs) have been shown to participate in the tumor pathogenesis and served as biomarkers for the clinical prognosis. However, the comprehensive analyses of the ceRNA network in the prognosis of MPM are still rarely reported. In this study, we obtained the transcriptome data of the MPM and the normal samples from TCGA, EGA, and GEO databases and identified the differentially expressed (DE) mRNAs, lncRNAs, and miRNAs. The functions of the prognostic genes and the overlapped DEmRNAs were further annotated by the multiple enrichment analyses. Then, the targeting relationships among lncRNA-miRNA and miRNA-mRNA were predicted and calculated, and a prognostic ceRNA regulatory network was established. We included the prognostic 73 mRNAs and 13 miRNAs and 26 lncRNAs into the ceRNA network. Moreover, 33 mRNAs, three miRNAs, and seven lncRNAs were finally associated with prognosis, and a model including seven mRNAs, two lincRNAs, and some clinical factors was finally established and validated by two independent cohorts, where CDK6 and SGMS1-AS1 were significant to be independent prognostic factors. In addition, the identified co-expressed modules associated with the prognosis were overrepresented in the ceRNA network. Multiple enrichment analyses showed the important roles of the extracellular matrix components and cell division dysfunction in the invasion of MPM potentially. In summary, the prognostic ceRNA network of MPM was established and analyzed for the first time and these findings shed light on the function of ceRNAs and revealed the potential prognostic and therapeutic biomarkers of MPM.
恶性胸膜间皮瘤(MPM)是一种侵袭性很强的癌症,生存时间短。失衡的竞争性内源性RNA(ceRNA)已被证明参与肿瘤发病机制,并作为临床预后的生物标志物。然而,关于MPM预后中ceRNA网络的综合分析仍鲜有报道。在本研究中,我们从TCGA、EGA和GEO数据库中获取了MPM和正常样本的转录组数据,鉴定了差异表达(DE)的mRNA、lncRNA和miRNA。通过多重富集分析进一步注释了预后基因和重叠的DEmRNA的功能。然后,预测并计算lncRNA-miRNA和miRNA-mRNA之间的靶向关系,建立了预后ceRNA调控网络。我们将73个预后mRNA、13个miRNA和26个lncRNA纳入ceRNA网络。此外,最终有33个mRNA、3个miRNA和7个lncRNA与预后相关,最终建立了一个包含7个mRNA、2个lincRNA和一些临床因素的模型,并通过两个独立队列进行了验证,其中CDK6和SGMS1-AS1是显著的独立预后因素。此外,在ceRNA网络中,与预后相关的共表达模块被过度富集。多重富集分析表明,细胞外基质成分和细胞分裂功能障碍可能在MPM侵袭中起重要作用。总之,首次建立并分析了MPM的预后ceRNA网络,这些发现揭示了ceRNA的功能,揭示了MPM潜在的预后和治疗生物标志物。