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  1. Article ; Online: Differentially expressed plasmatic microRNAs in Brazilian patients with Coronavirus disease 2019 (COVID-19): preliminary results.

    Nicoletti, Aline de Souza / Visacri, Marília Berlofa / da Ronda, Carla Regina da Silva Correa / Vasconcelos, Pedro Eduardo do Nascimento Silva / Quintanilha, Julia Coelho França / de Souza, Rafael Nogueira / Ventura, Deise de Souza / Eguti, Adriana / Silva, Lilian Ferreira de Souza / Perroud Junior, Mauricio Wesley / Catharino, Rodrigo Ramos / Reis, Leonardo Oliveira / Dos Santos, Luiz Augusto / Durán, Nelson / Fávaro, Wagner José / Lancellotti, Marcelo / da Costa, José Luiz / Moriel, Patricia / Pincinato, Eder de Carvalho

    Molecular biology reports

    2022  Volume 49, Issue 7, Page(s) 6931–6943

    Abstract: Background: Coronavirus disease 2019 (COVID-19) is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is known that host microRNAs (miRNAs) can be modulated to favor viral infection or to protect the host. ... ...

    Abstract Background: Coronavirus disease 2019 (COVID-19) is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is known that host microRNAs (miRNAs) can be modulated to favor viral infection or to protect the host. Herein, we report preliminary results of a study aiming at identifying differentially expressed plasmatic miRNAs in Brazilian patients with COVID-19.
    Methods and results: miRNAs were extracted from the plasma of eight patients with COVID-19 (four patients with mild COVID-19 and four patients with severe/critical COVID-19) and four healthy controls. Patients and controls were matched for sex and age. miRNA expression levels were detected using high-throughput sequencing. Differential miRNA expression and enrichment analyses were further evaluated. A total of 18 miRNAs were differentially expressed between patients with COVID-19 and controls. miR-4433b-5p, miR-6780b-3p, miR-6883-3p, miR-320b, miR-7111-3p, miR-4755-3p, miR-320c, and miR-6511a-3p were the most important miRNAs significantly involved in the PI3K/AKT, Wnt/β-catenin, and STAT3 signaling pathways. Moreover, 42 miRNAs were differentially expressed between severe/critical and mild patients with COVID-19. miR-451a, miR-101-3p, miR-185-5p, miR-30d-5p, miR-25-3p, miR-342-3p, miR-30e-5p, miR-150-5p, miR-15b-5p, and miR-29c-3p were the most important miRNAs significantly involved in the Wnt/β-catenin, NF-κβ, and STAT3 signaling pathways.
    Conclusions: If validated by quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) in a larger number of participants, the miRNAs identified in this study might be used as possible biomarkers for the diagnosis and severity of COVID-19.
    MeSH term(s) Brazil/epidemiology ; COVID-19/genetics ; Gene Expression Profiling/methods ; Humans ; MicroRNAs/metabolism ; Phosphatidylinositol 3-Kinases/genetics ; SARS-CoV-2 ; beta Catenin/genetics
    Chemical Substances MicroRNAs ; beta Catenin
    Language English
    Publishing date 2022-03-17
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 186544-4
    ISSN 1573-4978 ; 0301-4851
    ISSN (online) 1573-4978
    ISSN 0301-4851
    DOI 10.1007/s11033-022-07338-9
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Differentially expressed plasmatic microRNAs in Brazilian patients with Coronavirus disease 2019 (COVID-19): preliminary results

    Nicoletti, Aline de Souza / Visacri, Marília Berlofa / da Ronda, Carla Regina da Silva Correa / Vasconcelos, Pedro Eduardo do Nascimento Silva / Quintanilha, Julia Coelho França / de Souza, Rafael Nogueira / Ventura, Deise de Souza / Eguti, Adriana / Silva, Lilian Ferreira de Souza / Perroud Junior, Mauricio Wesley / Catharino, Rodrigo Ramos / Reis, Leonardo Oliveira / dos Santos, Luiz Augusto / Durán, Nelson / Fávaro, Wagner José / Lancellotti, Marcelo / da Costa, José Luiz / Moriel, Patricia / Pincinato, Eder de Carvalho

    Molecular biology reports. 2022 July, v. 49, no. 7

    2022  

    Abstract: BACKGROUND: Coronavirus disease 2019 (COVID-19) is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is known that host microRNAs (miRNAs) can be modulated to favor viral infection or to protect the host. ... ...

    Abstract BACKGROUND: Coronavirus disease 2019 (COVID-19) is caused by a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). It is known that host microRNAs (miRNAs) can be modulated to favor viral infection or to protect the host. Herein, we report preliminary results of a study aiming at identifying differentially expressed plasmatic miRNAs in Brazilian patients with COVID-19. METHODS AND RESULTS: miRNAs were extracted from the plasma of eight patients with COVID-19 (four patients with mild COVID-19 and four patients with severe/critical COVID-19) and four healthy controls. Patients and controls were matched for sex and age. miRNA expression levels were detected using high-throughput sequencing. Differential miRNA expression and enrichment analyses were further evaluated. A total of 18 miRNAs were differentially expressed between patients with COVID-19 and controls. miR-4433b-5p, miR-6780b-3p, miR-6883-3p, miR-320b, miR-7111-3p, miR-4755-3p, miR-320c, and miR-6511a-3p were the most important miRNAs significantly involved in the PI3K/AKT, Wnt/β-catenin, and STAT3 signaling pathways. Moreover, 42 miRNAs were differentially expressed between severe/critical and mild patients with COVID-19. miR-451a, miR-101-3p, miR-185-5p, miR-30d-5p, miR-25-3p, miR-342-3p, miR-30e-5p, miR-150-5p, miR-15b-5p, and miR-29c-3p were the most important miRNAs significantly involved in the Wnt/β-catenin, NF-κβ, and STAT3 signaling pathways. CONCLUSIONS: If validated by quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) in a larger number of participants, the miRNAs identified in this study might be used as possible biomarkers for the diagnosis and severity of COVID-19.
    Keywords COVID-19 infection ; Severe acute respiratory syndrome coronavirus 2 ; biomarkers ; microRNA ; molecular biology ; reverse transcriptase polymerase chain reaction
    Language English
    Dates of publication 2022-07
    Size p. 6931-6943.
    Publishing place Springer Netherlands
    Document type Article
    ZDB-ID 186544-4
    ISSN 1573-4978 ; 0301-4851
    ISSN (online) 1573-4978
    ISSN 0301-4851
    DOI 10.1007/s11033-022-07338-9
    Database NAL-Catalogue (AGRICOLA)

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