Evidence map›Paper›PMID 25143867›Full record

ArticleAmerican journal of clinical and experimental immunology2014

MicroRNA-570-3p regulates HuR and cytokine expression in airway epithelial cells.

Alanna N Roff, Timothy J Craig, Avery August, Cristiana Stellato, Faoud T Ishmael

Open access · greenAbstract read
In one paragraph

Article in American journal of clinical and experimental immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

25 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
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  6. Article
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  10. Article
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  13. Article
  14. MicroRNA-570 is a novel regulator of cellular senescence and inflammaging.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  15. Diagnostic Potential of Extracellular MicroRNA in Respiratory Diseases.Clinical reviews in allergy & immunology · 2018
    Review
  16. Article
  17. Effects of allergic stimulation and glucocorticoids on miR-155 in CD4American journal of clinical and experimental immunology · 2018
    Article
  18. Review
  19. Article
  20. Posttranslational control of HuR function.Wiley interdisciplinary reviews. RNA · 2017
    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

5 authors at 3 institutions in 2 countries.

Alanna N RoffDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Section of Allergy and Immunology, The Pennsylvania State University Milton S Hershey Medical Center 500 University Dr, Hershey, PA 17033, USA.
Timothy J CraigDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Section of Allergy and Immunology, The Pennsylvania State University Milton S Hershey Medical Center 500 University Dr, Hershey, PA 17033, USA.
Avery AugustDepartment of Microbiology and Immunology, Cornell University Ithaca, NY 14853.
Cristiana StellatoUniversity of Salerno Medicine Campus Via Salvador Allende, Baronissi (SA), 84081 Italy.
Faoud T IshmaelDepartment of Medicine, Division of Pulmonary, Allergy, and Critical Care Medicine, Section of Allergy and Immunology, The Pennsylvania State University Milton S Hershey Medical Center 500 University Dr, Hershey, PA 17033, USA ; Department of Biochemistry and Molecular Biology, The Pennsylvania State University College of Medicine 500 University Dr, Hershey, PA 17033, USA.
Penn State Milton S. Hershey Medical Center · USCornell University · USUniversity of Salerno · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asthma is a chronic lung disease that affects people of all ages and is characterized by high morbidity. The mechanisms of asthma pathogenesis are unclear, and there is a need for development of diagnostic biomarkers and greater understanding of regulation of inflammatory responses in the lung. Post-transcriptional regulation of cytokines, chemokines, and growth factors by the action of microRNAs and RNA-binding proteins on stability or translation of mature transcripts is emerging as a central means of regulating the inflammatory response. In this study, we demonstrate that miR-570-3p expression is increased with TNFα stimuli in normal human bronchial epithelial cells (2.6 ± 0.6, p = 0.01) and the human airway epithelial cell line A549 (4.6 ± 1.4, p = 0.0068), and evaluate the functional effects of its overexpression on predicted mRNA target genes in transfected A549 cells. MiR-570-3p upregulated numerous cytokines and chemokines (CCL4, CCL5, TNFα, and IL-6) and also enhanced their induction by TNFα. For other cytokines (CCL2 and IL-8), the microRNA exhibited an inhibitory effect to repress their upregulation by TNFα. These effects were mediated by a complex pattern of both direct and indirect regulation of downstream targets by miR-570-3p. We also show that the RNA-binding protein HuR is a direct target of miR-570-3p, which has implications for expression of numerous other inflammatory mediators that HuR is known regulate post-transcriptionally. Finally, expression of endogenous miR-570-3p was examined in both serum and exhaled breath condensate (EBC) from asthmatic and healthy patients, and was found to be significantly lower in EBC of asthmatics and inversely correlated to their lung function. These studies implicate miR-570-3p as a potential regulator of asthmatic inflammation with potential as both a diagnostic and therapeutic target in asthma.

Indexed as

airwayasthmabiomarkercytokinesinflammationMicroRNApost-transcriptional regulation

Identifiers

PMID25143867
PMCPMC4138130
OpenAlexW1937512539

What OpenQuestion 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 OpenQuestion graph.