Wu Dan, Yang Nana, Xu Yetao, Wang Sailan, Zhang Yuanyuan, Sagnelli Matthew, Hui Bingqing, Huang Zhenyao, Sun Lizhou
Department of Obstetrics and Gynecology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China; Department of Neurobiology, Care Science and Society, Karolinska Institutet, Solna 17177, Sweden.
Department of Obstetrics and Gynecology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, Jiangsu Province, China.
Mol Ther Nucleic Acids. 2019 Jun 7;16:605-615. doi: 10.1016/j.omtn.2019.04.009. Epub 2019 Apr 18.
Long noncoding RNAs (lncRNAs) have been reported to be involved in various human diseases, and increasing studies have revealed that lncRNAs can play a vital role in preeclampsia (PE). In our study, lncRNA hypoxia-inducible factor 1 alpha (HIF1A) antisense RNA 2 (HIF1A-AS2) was found to be significantly downregulated in placenta tissues of PE patients by quantitative real-time PCR analysis. Moreover, Cell Counting Kit-8 (CCK-8) assays showed that downregulation of HIF1A-AS2 can impede cell proliferation of HTR-8/SVneo and JAR trophoblasts cells. Ectopic overexpression of HIF1A-AS2 can increase the function of trophoblasts cell migration and invasion in vitro. RNA-sequencing (RNA-seq), RNA immunoprecipitation (RIP), and chromatin immunoprecipitation (ChIP) experiments showed that HIF1A-AS2 can recruit lysine-specific demethylase 1 (LSD1) and epigenetically repress pleckstrin homology-like domain, family A, member 1 (PHLDA1) transcription in human trophoblasts cells. In summary, our findings suggest that downregulated HIF1A-AS2 may play a role in the pathogenesis and progression of PE, and has potential as a novel prognostic marker in PE.
据报道,长链非编码RNA(lncRNAs)参与多种人类疾病,越来越多的研究表明lncRNAs在子痫前期(PE)中可发挥重要作用。在我们的研究中,通过定量实时PCR分析发现,lncRNA缺氧诱导因子1α(HIF1A)反义RNA 2(HIF1A-AS2)在PE患者的胎盘组织中显著下调。此外,细胞计数试剂盒-8(CCK-8)检测表明,HIF1A-AS2的下调会阻碍HTR-8/SVneo和JAR滋养层细胞的细胞增殖。HIF1A-AS2的异位过表达可增强滋养层细胞在体外的迁移和侵袭功能。RNA测序(RNA-seq)、RNA免疫沉淀(RIP)和染色质免疫沉淀(ChIP)实验表明,HIF1A-AS2可招募赖氨酸特异性去甲基化酶1(LSD1),并在表观遗传上抑制人滋养层细胞中pleckstrin同源样结构域A家族成员1(PHLDA1)的转录。总之,我们的研究结果表明,HIF1A-AS2的下调可能在PE的发病机制和进展中起作用,并具有作为PE新型预后标志物的潜力。