Li Fangwei, Shi Wenhua, Wan Yixin, Wang Qingting, Feng Wei, Yan Xin, Wang Jian, Chai Limin, Zhang Qianqian, Li Manxiang
Department of Respiratory Medicine The First Affiliated Hospital of Xi'an Jiaotong University China.
Department of Respiratory Medicine Lanzhou University Second Hospital China.
FEBS Open Bio. 2017 Oct 21;7(12):1880-1890. doi: 10.1002/2211-5463.12322. eCollection 2017 Dec.
The expression of microRNA (miR)-140-5p is known to be reduced in both pulmonary arterial hypertension (PAH) patients and monocrotaline-induced PAH models in rat. Identification of target genes for miR-140-5p with bioinformatics analysis may reveal new pathways and connections in PAH. This study aimed to explore downstream target genes and relevant signaling pathways regulated by miR-140-5p to provide theoretical evidences for further researches on role of miR-140-5p in PAH. Multiple downstream target genes and upstream transcription factors (TFs) of miR-140-5p were predicted in the analysis. Gene ontology (GO) enrichment analysis indicated that downstream target genes of miR-140-5p were enriched in many biological processes, such as biological regulation, signal transduction, response to chemical stimulus, stem cell proliferation, cell surface receptor signaling pathways. Kyoto Encyclopedia of Genes and Genome (KEGG) pathway analysis found that downstream target genes were mainly located in Notch, TGF-beta, PI3K/Akt, and Hippo signaling pathway. According to TF-miRNA-mRNA network, the important downstream target genes of miR-140-5p were PPI, TGF-betaR1, smad4, JAG1, ADAM10, FGF9, PDGFRA, VEGFA, LAMC1, TLR4, and CREB. After thoroughly reviewing published literature, we found that 23 target genes and seven signaling pathways were truly inhibited by miR-140-5p in various tissues or cells; most of these verified targets were in accordance with our present prediction. Other predicted targets still need further verification and .
已知在肺动脉高压(PAH)患者以及大鼠野百合碱诱导的PAH模型中,微小RNA(miR)-140-5p的表达均降低。通过生物信息学分析鉴定miR-140-5p的靶基因,可能会揭示PAH中的新途径和联系。本研究旨在探索受miR-140-5p调控的下游靶基因和相关信号通路,为进一步研究miR-140-5p在PAH中的作用提供理论依据。在分析中预测了miR-140-5p的多个下游靶基因和上游转录因子(TFs)。基因本体论(GO)富集分析表明,miR-140-5p的下游靶基因在许多生物学过程中富集,如生物调节、信号转导、对化学刺激的反应、干细胞增殖、细胞表面受体信号通路。京都基因与基因组百科全书(KEGG)通路分析发现,下游靶基因主要位于Notch、TGF-β、PI3K/Akt和Hippo信号通路中。根据TF-miRNA-mRNA网络,miR-140-5p的重要下游靶基因为PPI、TGF-βR1、smad4、JAG1、ADAM10、FGF9、PDGFRA、VEGFA、LAMC1、TLR4和CREB。在全面查阅已发表的文献后,我们发现23个靶基因和7条信号通路在各种组织或细胞中确实受到miR-140-5p的抑制;这些已验证的靶标大多与我们目前的预测一致。其他预测的靶标仍需进一步验证。