Evidence map›Paper›PMID 35062245›Full record

ReviewViruses2021

miRNAs, from Evolutionary Junk to Possible Prognostic Markers and Therapeutic Targets in COVID-19.

Brandon Bautista-Becerril, Guillermo Pérez-Dimas, Paola C Sommerhalder-Nava, Alejandro Hanono, Julio A Martínez-Cisneros, Bárbara Zarate-Maldonado, Evangelina Muñoz-Soria, Arnoldo Aquino-Gálvez, Manuel Castillejos-López, Armida Juárez-Cisneros and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
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

22 citing papers in PubMed, 24 citations in OpenAlex.

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  17. COVID-19 therapies: do we see substantial progress?Cellular & molecular biology letters · 2022
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  18. Review
  19. miRNAs: The Key Regulator of COVID-19 Disease.International journal of cell biology · 2022
    Review
  20. Article
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

12 authors at 3 institutions in 1 country.

Brandon Bautista-BecerrilLaboratorio HLA, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.
Guillermo Pérez-DimasEscuela Superior de Medicina, Departamento de Posgrado, Instituto Politécnico Nacional, Mexico City 11340, Mexico.
Paola C Sommerhalder-NavaFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Mexico City 52786, Mexico.
Alejandro HanonoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Mexico City 52786, Mexico.ORCID 0000-0002-6235-124X
Julio A Martínez-CisnerosOrganismo Público Descentralizado, Servicios de Salud Jalisco, Zapopan City 45010, Mexico.
Bárbara Zarate-MaldonadoFacultad de Ciencias de la Salud, Universidad Anáhuac México Norte, Mexico City 52786, Mexico.
Evangelina Muñoz-SoriaEscuela Superior de Medicina, Departamento de Posgrado, Instituto Politécnico Nacional, Mexico City 11340, Mexico.
Arnoldo Aquino-GálvezLaboratorio de Biología Molecular, Departamento de Fibrosis Pulmonar, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.ORCID 0000-0002-2869-5516
Manuel Castillejos-LópezDepartamento de Epidemiología Hospitalaria e Infectología, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.ORCID 0000-0001-8689-9755
Armida Juárez-CisnerosLaboratorio HLA, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.
Jose S Lopez-GonzalezLaboratorio de Cáncer Pulmonar, Departamento de Enfermedades Crónico-Degenerativas, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.
Angel CamarenaLaboratorio HLA, Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City 14080, Mexico.
Instituto Nacional de Enfermedades Respiratorias · MXUniversidad Anáhuac · MXInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic has been a public health issue around the world in the last few years. Currently, there is no specific antiviral treatment to fight the disease. Thus, it is essential to highlight possible prognostic predictors that could identify patients with a high risk of developing complications. Within this framework, miRNA biomolecules play a vital role in the genetic regulation of various genes, principally, those related to the pathophysiology of the disease. Here, we review the interaction of host and viral microRNAs with molecular and cellular elements that could potentiate the main pulmonary, cardiac, renal, circulatory, and neuronal complications in COVID-19 patients. miR-26a, miR-29b, miR-21, miR-372, and miR-2392, among others, have been associated with exacerbation of the inflammatory process, increasing the risk of a cytokine storm. In addition, increased expression of miR-15b, -199a, and -491 are related to the prognosis of the disease, and miR-192 and miR-323a were identified as clinical predictors of mortality in patients admitted to the intensive care unit. Finally, we address miR-29, miR-122, miR-155, and miR-200, among others, as possible therapeutic targets. However, more studies are required to confirm these findings.

Indexed as

COVID-19 Drug TreatmentAntiviral AgentsCOVID-19Drug Delivery SystemsHost-Pathogen InteractionsHumansInflammationMicroRNAsPrognosisRNA, ViralSARS-CoV-2Antiviral AgentsMicroRNAsRNA, ViralcomplicationsCOVID-19miRNAprognosisSARS-CoV-2therapeuticvirus

Identifiers

PMID35062245
PMCPMC8781105
OpenAlexW4200209032

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.