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Identification of Potential Key Long Non-Coding RNAs and Target Genes Associated with Pneumonia Using Long Non-Coding RNA Sequencing (lncRNA-Seq): A Preliminary Study.
Huang, Sai; Feng, Cong; Chen, Li; Huang, Zhi; Zhou, Xuan; Li, Bei; Wang, Li-Li; Chen, Wei; Lv, Fa-Qin; Li, Tan-Shi.
Afiliação
  • Huang S; Department of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
  • Feng C; Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
  • Chen L; Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
  • Huang Z; Department of Electrical and Computer Engineering, Purdue University, Indianapolis, IN, USA.
  • Zhou X; Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
  • Li B; Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
  • Wang LL; Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
  • Chen W; Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
  • Lv FQ; Department of Ultrasound, General Hospital of the PLA, Beijing, China (mainland).
  • Li TS; Department of Emergency, General Hospital of the PLA, Beijing, China (mainland).
Med Sci Monit ; 22: 3394-3408, 2016 Sep 24.
Article em En | MEDLINE | ID: mdl-27663962
BACKGROUND This study aimed to identify the potential key long non-coding RNAs (lncRNAs) and target genes associated with pneumonia using lncRNA sequencing (lncRNA-seq). MATERIAL AND METHODS A total of 9 peripheral blood samples from patients with mild pneumonia (n=3) and severe pneumonia (n=3), as well as volunteers without pneumonia (n=3), were received for lncRNA-seq. Based on the sequencing data, differentially expressed lncRNAs (DE-lncRNAs) were identified by the limma package. After the functional enrichment analysis, target genes of DE-lncRNAs were predicted, and the regulatory network was constructed. RESULTS In total, 99 DE-lncRNAs (14 upregulated and 85 downregulated ones) were identified in the mild pneumonia group and 85 (72 upregulated and 13 downregulated ones) in the severe pneumonia group, compared with the control group. Among these DE-lncRNAs, 9 lncRNAs were upregulated in both the mild and severe pneumonia groups. A set of 868 genes were predicted to be targeted by these 9 DE-lncRNAs. In the network, RP11-248E9.5 and RP11-456D7.1 targeted the majority of genes. RP11-248E9.5 regulated several genes together with CTD-2300H10.2, such as QRFP and EPS8. Both upregulated RP11-456D7.1 and RP11-96C23.9 regulated several genes, such as PDK2. RP11-456D7.1 also positively regulated CCL21. CONCLUSIONS These novel lncRNAs and their target genes may be closely associated with the progression of pneumonia.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Med Sci Monit Assunto da revista: MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Risk_factors_studies Idioma: En Revista: Med Sci Monit Assunto da revista: MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de publicação: Estados Unidos