Evidence map›Paper›PMID 37380930›Full record

ArticleArchives of virology2023

Circulating microRNA profile in response to remdesivir treatment in coronavirus disease 2019 (COVID-19) patients.

Mohammad Fayyad-Kazan, Rawan Makki, Mahmoud El Homsi, Ahmad Samadi, Hilal Chaaban, Rania El Majzoub, Eva Hamade, Hussein Fayyad-Kazan, Bassam Badran

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mohammad Fayyad-Kazan *Department of Natural and Applied Sciences, School of Arts and Sciences, The American University of Iraq-Baghdad, Baghdad, Iraq. mfayyadk@gmail.com.ORCID http://orcid.org/0000-0001-8442-1619
Rawan Makki *Laboratory of Cancer biology and Molecular Immunology, Faculty of Sciences-I, Lebanese University, Hadath-Beirut, Lebanon.
Mahmoud El HomsiLaboratory of Cancer biology and Molecular Immunology, Faculty of Sciences-I, Lebanese University, Hadath-Beirut, Lebanon.
Ahmad SamadiMolecular diagnostics Laboratory, Saida Governmental Hospital, Saida, Lebanon.
Hilal ChaabanMolecular diagnostics Laboratory, Saida Governmental Hospital, Saida, Lebanon.
Rania El MajzoubLaboratory of Cancer biology and Molecular Immunology, Faculty of Sciences-I, Lebanese University, Hadath-Beirut, Lebanon.
Eva HamadeLaboratory of Cancer biology and Molecular Immunology, Faculty of Sciences-I, Lebanese University, Hadath-Beirut, Lebanon.
Hussein Fayyad-Kazan *Laboratory of Cancer biology and Molecular Immunology, Faculty of Sciences-I, Lebanese University, Hadath-Beirut, Lebanon.
Bassam Badran *Laboratory of Cancer biology and Molecular Immunology, Faculty of Sciences-I, Lebanese University, Hadath-Beirut, Lebanon. bassam.badran@ul.edu.lb.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19), a serious infectious disease caused by the recently discovered severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has caused a major global health crisis. Although no specific antiviral drugs have been proven to be fully effective against COVID-19, remdesivir (GS-5734), a nucleoside analogue prodrug, has shown beneficial effects when used to treat severe hospitalized COVID-19 cases. The molecular mechanism underlying this beneficial therapeutic effect is still vaguely understood. In this study, we assessed the effect of remdesivir treatment on the pattern of circulating miRNAs in the plasma of COVID-19 patients, which was analyzed using MiRCURY LNA miRNA miRNome qPCR Panels and confirmed by quantitative real-time RT-PCR (qRT-PCR). The results revealed that remdesivir treatment can restore the levels of miRNAs that are upregulated in COVID-19 patients to the range observed in healthy subjects. Bioinformatics analysis revealed that these miRNAs are involved in diverse biological processes, including the transforming growth factor beta (TGF-β), hippo, P53, mucin-type O-glycan biosynthesis, and glycosaminoglycan biosynthesis signaling pathways. On the other hand, three miRNAs (hsa-miR-7-5p, hsa-miR-10b-5p, and hsa-miR-130b-3p) were found to be upregulated in patients receiving remdesivir treatment and in patients who experienced natural remission. These upregulated miRNAs could serve as biomarkers of COVID-19 remission. This study highlights that the therapeutic potential of remdesivir involves alteration of certain miRNA-regulated biological processes. Targeting of these miRNAs should therefore be considered for future COVID-19 treatment strategies.

Indexed as

Circulating MicroRNACOVID-19MicroRNAsAdenosine MonophosphateAlanineCOVID-19 Drug TreatmentHumansSARS-CoV-2Adenosine MonophosphateAlanineCirculating MicroRNAMicroRNAsremdesivir

Identifiers

PMID37380930

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.