Detection of the long noncoding RNAs nuclear-enriched autosomal transcript 1 (NEAT1) and metastasis associated lung adenocarcinoma transcript 1 in the peripheral blood of HIV-1-infected patients.

Objectives: Long noncoding RNAs (lncRNAs) in HIV-1 infection have not been extensively studied. Here we detected two lncRNAs, nuclear-enriched autosomal transcript 1 (NEAT1) and metastasis associated lung adenocarcinoma transcript 1 (MALAT1), in peripheral blood mononuclear cells (PBMCs) and plasma...

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Publicado en:HIV Medicine Vol. 17; no. 1; pp. 68 - 73
Autores principales: Jin, C, Peng, X, Xie, T, Lu, X, Liu, F, Wu, H, Yang, Z, Wang, J, Cheng, L, Wu, N
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Jan2016
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jan2016
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1111/hiv.12276
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        atl: Detection of the long noncoding RNAs nuclear-enriched autosomal transcript 1 (NEAT1) and metastasis associated lung adenocarcinoma transcript 1 in the peripheral blood of HIV-1-infected patients.
      aug:
        au:
          Jin, C
          Peng, X
          Xie, T
          Lu, X
          Liu, F
          Wu, H
          Yang, Z
          Wang, J
          Cheng, L
          Wu, N
        affil: State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou China
      sug:
        subj:
          RNA
          HIV Infections
          Adenocarcinoma
          Human
          HIV-Positive Persons
          Neoplasm Metastasis
          Lung
          Anti-Retroviral Agents
          Antiretroviral Therapy, Highly Active
          Biological Markers
      ab: Objectives: Long noncoding RNAs (lncRNAs) in HIV-1 infection have not been extensively studied. Here we detected two lncRNAs, nuclear-enriched autosomal transcript 1 (NEAT1) and metastasis associated lung adenocarcinoma transcript 1 (MALAT1), in peripheral blood mononuclear cells (PBMCs) and plasma of HIV-1-infected patients. Methods: Fifty-nine HIV-1-infected patients and 21 healthy controls were recruited for the study, of whom 31 patients were highly active antiretroviral therapy (HAART)-naïve and 28 patients had been receiving HAART for more than 1 year with undetectable viral loads. Total RNA was extracted from PBMCs and plasma, and levels of NEAT1 and MALAT1 were determined by quantitative real-time polymerase chain reaction. Results: We found that the levels of NEAT1 and MALAT1 in PBMCs were up-regulated in HAART-naïve patients and were reduced in patients receiving HAART. NEAT1 was down-regulated in the plasma of infected patients and expression was correlated with CD4 T-cell count. Conclusions: Our findings suggest that NEAT1 and MALAT1 may interact with HIV-1 in vivo and that the presence of NEAT1 in plasma is a potential biomarker of HIV-1 infection.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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